Title of Invention	HYDRATES OF TRIAZINYLAMINOSTILBENE COMPOUNDS AND PROCESS FOR PREPARING THE SAME
Abstract	The present invention provides a hydrate of the 4,4'-di-triazinylamino-2,2'-di- sulfostilbene compound having the formula: in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di- sulfostilbene compound having the formula (I); processes for the preparation of the new hydrates; and the use of the new hydrates for the preparation of concentrated aqueous formulations of fluorescent whitening agents.

Title of Invention

HYDRATES OF TRIAZINYLAMINOSTILBENE COMPOUNDS AND PROCESS FOR PREPARING THE SAME

Abstract

The present invention provides a hydrate of the 4,4'-di-triazinylamino-2,2'-di- sulfostilbene compound having the formula: in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di- sulfostilbene compound having the formula (I); processes for the preparation of the new hydrates; and the use of the new hydrates for the preparation of concentrated aqueous formulations of fluorescent whitening agents.

Full Text	The present invention relates to the novel hydrates of the salts of a specific 4.4'-di-triazinylamino-2,2'-di-sulfostilbene compound, characterised by their water of hydration content; to the crystal forms which are associated with the new hydrates and which are characterised by their X-ray diffraction pattern; to processes for the preparation of the new hydrates; and to the use of the new hydrates for the preparation of concentrated formulations of fluorescent whitening agents. According to recent practice, fluorescent whitening agents are preferably put on the market in the form of aqueous solutions or suspensions. To this end, for example, the moist filtercakes or dry powders of the fluorescent whitening agents are suspended in water Dispersants and thickeners are added to the suspension in order to increase the homogeneity, wettability and shelf life of the suspension. Frequently, an electrolyte is also added together with these auxiliaries. Despite the presence of these additives, there are concentration limits for the fluorescent whitening agent suspension, above which the suspension is often unstable on storage and has poor metering characteristics. These concentration limits are often difficult to reproduce, since they can be affected by the nature of a pretreatment which may have been applied to the suspension of the fluorescent whitening agent. In particular, depending on the nature of a pretreatment, a variety of hydrates of the fluorescent whitening agent, having different crystal forms, may be obtained. Surprisingly, it has now been found that formulations of a specific fluorescent whitening agent, which have an active substance concentration of more than 30% by weight, which are stable on storage and the viscosity of which can be selectively set at a value within a wide range, can be prepared if a specific hydrate or mixtures of hydrates of the fluorescent whitening agent used, having a specific crystal form, or several specific crystal forms, are present. The new formulations contain only low amounts of formulation auxiliaries and are useful for the fluorescent whitening of a wide range of substrates, including textiles and paper. in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'"di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I). Preferred hydrates of formula (I) are compounds in which M and Mi both represent hydrogen or sodium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 7; or a mixture containing one or more of the hydrates of the di-sodium salt of the 4,4'-di-triazinylamino-2,2'-di-suIfostiibene compound having the formula (I). Further preferred hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound (I) are those in which M and M1 both represent potassium, the hydrate being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figure 8 and in which x represents 9 to 17 and those in which M and M1 both represent lithium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 9 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di- triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and Mi representing lithium and in which x represents 9 to 30. Further hydrates of interest are such hydrates of the 4,4-di-triazinylamino-2,2'-dJ-sulfostilbene compound (I) in which M and Mi both represent calcium or magnesium and also those in which M and Mi both represent ammonium. In compounds of formula (I) in which M and Mi both represent ammonium these may be represented by the formula -N(R)4,whereby R represents hydrogen or Cr C4-alkyl, all R-groups not necessarily being identical, or C2-C4-alkanolammonium. The respective X-ray diffraction patterns, Figures 1 to 11, are obtained using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The reference patterns for crystal forms B (Figure 1) and C (Figure 2) are measured in suspensions in an atmosphere of air, without control of relative humidity. The measurement of the reference patterns for crystal form D (Figure 3), E (Figure 4), F (Figure 6) and G (Figure 7) and also that of the di-potassium salt (Figure 8) are also conducted in suspensions, under nitrogen, while maintaining the relative humidity at a level of 80-90%, as are those of the three crystal forms of the di-lithium salt (Figures 9-11). whilst that of crystal form A (Figure 5) was conducted in the solid state. In each of the accompanying Figures 1 to 11. there is shown the part of the measurements in the 20-area between 1 and 30° Each of the novel hydrates of formula (I) has a characteristic X-ray diffraction pattern. The crystal forms A, B, C, D, E, F and G and also those of the di-potassium and lithium salts consist for the most part of one or more hydrates of the formula (I) in which X is a number between 1 and 30. The amount of water of hydration may be determined via . differential thermal analysis or dynamic differential calorimetry in which the proportion of the unbound water, that is the water melting at 0°C, is measured, or by subsequent water analysis by methods such as Karl Fischer titration, thermogravimetric analysis or loss on drying at elevated temperature. The di-sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form may be produced by successively reacting cyanuric chloride with 4,4'-diaminostiibene disulphonic acid di-sodium salt, aniline and diethanoiamine, adjusting the pH of the mixture to 9.0 to 9.5 with concentrated sodium hydroxide solution and evaporating the mixture to dryness. If, prior to treatment with sodium hydroxide, the compound is isolated in the form of the free acid, a hydrate results possessing the (F) crystal form. The (C) hydrate crystal form may be obtained by neutralization of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with dilute sodium hydroxide solution, homogenising and allowing to stand at room temperature; the (D) hydrate crystal form by treatment of the sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form aqueous sodium chloride solution, stabilizing and homogenising; and the (E) hydrate crystal form by treatment of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with concentrated sodium hydroxide solution and homogenising. The (G) crystal form of the hydrate may be obtained from the (E) form by equilibration in a closed vessel at elevated temperature. The (C) hydrate can further be prepared by seeding an aqueous suspension of the corresponding free acid, with (C) seed crystals. This technique has the advantage that active substance concentrations of more than 30% by weight, preferably 30 to 50% by weight, can be used and thus the suspension obtained is formed in the desired concentration and does not have to be concentrated. The hydrate of crystal form (D) in accordance with Figure 3, or the hydrate of crystal form which is designated as (E) form and characterised by an X-ray diffraction pattern which is essentially as in Figure 4, may also be prepared by the seeding technique described in relation to the production of the (C) form. In a preferred embodiment, a mixture of one or more of the novel hydrates of formula (I) is prepared by the controlled mixing of an aqueous solution of an inorganic salt electrolyte, preferably an alkali metal halide or sulfate, especially sodium chloride or sodium sulfate; and the active substance of formula (I). The process is conveniently conducted by firstly preparing an aqueous solution of the electrolyte and then seeding this electrolyte solution with a previously-prepared sample of the active substance of formula (I). While maintaining the pH value of the seeded electrolyte solution within the range of from 7.5 to 9.0, preferably from 8.0 to 8.5, active substance of formula (I), as the free acid, alkali, preferably sodium hydroxide and water are preferably added, simultaneously and portionwise, to the seeded electrolyte solution. Preferably, water and the free acid form of the active substance are added until a) the content of the active substance in the synthesis mixture is within the range of from 5 to 40%, preferably from 10 to 30% and especially from 15 to 25% by weight and b) the content of electrolyte in the synthesis mixture is within the range of from 0.5 to 2.5%, preferably from 1 to 2% and especially about 1.5% by weight. The seed crystals should be used in the form of small crystals whose average size does not markedly exceed 10 micron. This allows the substantial reduction of the seed crystal content, for example down to 0.1 to 5% by weight, relative to the total active substance content. The seeding is preferably effected without stirring. The seed crystal content is in general between 0.1 and 60% by weight, preferably between 1 and 50% by weight, and particulariy preferably between 1 and 30% by weight, relative to the total active substance content. In all cases in which only a portion of the final compound is replaced by new starting material, the conversion can be carried out as semi-continuous or continuous process. The reaction temperature for preparing the mixtures of hydrate of formula (I) according to the present invention preferably lies within the range of from 10-95°C and preferably within the range of from 35-55°C. The di-potassium and lithium salts of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene (I) may be obtained by neutralising the free acid form of 4,4'-di-triazinylamino-2,2'-di- sulfostilbene with potassium or lithium hydroxide, respectively. In the case of the di-lithium salt, two further crystal forms of the hydrates may be obtained by equilibrating a slurry of the salt obtained directly by neutralisation at elevated temperatures. The invention also provides an aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms of the formula (I). This formulation remains flowable, has good metering characteristics and is stable for months, without forming sediments, even after standing at temperatures of between 5-40°C for an extended period of time. An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms A, B, C, D, E, F and G of the formula (I) is highly viscous when no formulation auxiliaries are added and is suitable for the production of brushable pastes or for being incorporated therein. Thus, by incorporating the active substance in the form of one or more of novel hydrate forms of the formula (I) having different crystal forms, a desired viscosity of an aqueous formulation can be selectively established, without the presence of any further auxiliaries. An electrolyte, for example NaCI or Na2S04, or a mixture thereof, can be admixed with the aqueous formulation in order to stabilise the hydrates contained therein. A particular advantage of the hydrates according to the present invention having different crystal forms is that they enable ready-to-use and stable formulations of a wide range of viscosities to be produced, without addition of ecologically harmful formulation auxiliaries. If desired, however, the formulations obtained according to the present invention may contain customary formulation auxiliaries, such as dispersing agents, builders, protective colloids, stabilisers, preservatives, perfumes and sequestering agents. Dispersing agents are preferably anionic dispersing agents, such as condensation products of aromatic sulfonic acids with formaldehyde, for example ditolylethersulfonic acid, a naphthalenesulfonate or a ligninsulfonate. Examples of suitable builders or protective colloids are modified polysaccharides derived from cellulose or heteropolysaccharides, such as xanthan, carboxymethylcellulose and polyvinyl alcohols (PVA), polyvinylpyrrolidones (PVP), polyethylene glycols (PEG) and aluminium silicates or magnesium silicates. They are usually used in a concentration range of 0.01 to 2% by weight and preferably 0.05 to 0.5% by weight, relative to the total weight of the formulation. Examples of auxiliaries which can be used for stabilisation are ethylene glycol, propylene glycol or dispersants in an amount of 0.2 to 5% by weight and preferably 0.3 to 2% by eight, relative to the total weight of the formulation. Compounds which may be used as stabilisers include 1,2-benzisothiazolin-3-one, formaldehyde or chloroacetamide in an amount of 0.1 to 1% by weight and preferably 0.1 to 0,5% by weight relative to the total weight of the formulation. The concentrated formulation thus prepared can be used for the fluorescent whitening of paper or textile material, for example in detergents. To this end, they are in general diluted to the optimum concentration for the practical application by the addition of further auxiliaries or water. The following Examples further illustrate the present invention. Parts and percentages shown therein are by weight unless otherwise stated. Example 1 In a reaction vessel, 400g of ice, 120g of cyanuric chloride and 785g of methyl ethyl ketone are mixed and, with intensive stirring and external cooling, treated with a solution of 120g of 4,4'-diaminostilbene-2,2'-disulphonic acid disodium salt in 800g of water and 164.5g of 17% sodium carbonate solution over 20 minutes at 5-10°C, the pH being maintained at 4.5 by the simultaneous addition of 39.4g of 17% sodium carbonate solution. After the addition, 55.4g of aniline and 8,7g of diethanolamine are added, the pH being maintained at 7.5 by the simultaneous addition of 72.2g of 36% sodium hydroxide solution. After heating to 60°C, 78.8g of diethanolamine are added whilst maintaining the pH at 8.2 by the simultaneous addition of 72.2g of 36% sodium hydroxide solution. The reaction mixture is heated to reflux and the methyl ethyl ketone destilled off, being gradually replaced by 1000g of water. At a temperature of 95°C, the mixture is acidified to pH 4.5 by the addition of 170g of 16% hydrochloric acid solution and the volume adjusted to 2.71 by addition of water. After cooling to 70°C, the mixture is filtered and the filter cake washed with 1.81 of water to yield the free acid. A 30% aqueous suspension of this free acid is heated to 95°C and the pH adjusted to 9.0-9.5 by the addition of 36% sodium hydroxide solution. The resulting solution is then evaporated to dryness to yield a compound of Formula (1) as the di-sodium salt, which has the A-crystal form containing 1 mole of water, corresponding to the X-ray diffraction pattern which is set out in the accompanying Figure 5. Example 2 75.0 g of the free acid form (having an active substance content of 40% by weight) of the di-sodium salt of formula (I) are dispersed in 24.7 g of deionised water at 25°'C. The dispersion so obtained is stabilised by adding to it 0.2 g of xanthan gum and 0.1 g of Proxe! GXL (1,2-benzisothiazolin"3-one) and the mixture is homogenised. The homogenised suspension is neutralised with 32.8 mis of a 2N aqueous sodium hydroxide solution. The homogenised, neutralised suspension has the B-crystal form which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 1. After standing for two days at 25°C., a suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 2. Using the same procedure, but using, as starting material, the di-sodium salt of formula (I) in the form of a pure hydrate of the A, B, D, E, F or G crystal form, or a mixture thereof, a suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water, which corresponds to the X-ray diffraction pattern which (s set out in the accompanying Figure 2. Example 3 700g of the moist filter cake from Example 1 (= 265g of free acid) are gradually added to 314g of water at 40-45°C whilst maintaining the pH at 8 J-9.1 by the simultaneous addition of 64g of 36% sodium hydroxide solution. Then, at 42°C. 20g of seed crystals of the C form of the hydrate obtained in Example 2 are added. After 5 hours, the liquid dispersion is cooled to 25-30°C and stabilised by the addition of 2.2g of 50% glutaraldehyde solution and 2.2g of xanthan gum (polysaccharide), predispersed in 5.5g of propylene glycol. A liquid suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 2.' Example 4 In a reaction flask, 400 g of a 6% aqueous sodium chloride solution are preheated to 60°C. Into this solution are introduced 120 g of the di-sodium salt of formula (I) (having an active substance content of 90% by weight and containing 10% sodium chloride) and the mixture is heated to 90°C. 180 g of 6% aqueous sodium chloride solution are added and the mixture is cooled, with stirring, to 25°C, The resulting liquid suspension is stabilised by the addition of 2.45 g of xanthan gum which has been pre-dispersed in 6.1 g of 1,2-propylene glycol and the mixture is heated to 90°C. for two hours. The mixture is cooled, with stirring, to 25°C., 3.22 g of Proxel GXL (1,2-benzisothiazolin-3-one) are added, as stabiliser, the mixture is stirred for a further twelve hours and finally homogenised using a high speed stirrer A suspension is obtained which has the D-crystal form containing 14 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 3. Example 5 In a reaction flask, 400 mis of deionised water are pre-heated to 40°C. Into this water are introduced, portionwise, 800 g of the free acid form (having an active substance content of 40% by weight) of the di-sodium salt of formula (I) and, by the simultaneous portionwise addition of 50.45 mis of a 37% (50% g/v %) aqueous sodium hydroxide solution, the pH value of the mixture is kept constant at 8.2. After the addition is complete, the whole is diluted with 400 mis of deionised water, stirred for one hour and then homogenised. A suspension is obtained which has the E-crystal form containing 14 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 4. Example 6 620g of the moist filter cake obtained as in Example 1 (= 279g free acid) are dispersed in 304g of water and stabilised by the addition of 1.7g of Proxel GXL and 1.7g of xanthan gum (polysaccharide), predispersed in 3.3g of propylene glycol. A liquid suspension is obtained which has the F crystal form containing 7 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 6. Example 7 A 20% slurry of the E crystal form of the hydrate, obtained as in Example 5, is stirred in a closed vessel at 60°C and maintained at this temperature for at least 20 hours. After cooling to room temperature, a liquid suspension is obtained which has the G crystal form containing 7 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 7. Example 8 400 mis of a 6.0 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (II). The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (II), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 1.5% by weight. The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The device is fitted with a closed sample chamber (Anton Parr) which can be adapted to be purged with gas. The aqueous formulation is filled tel quel into the sample carrier (layer thickness 0.8 mm) and the measurement of the powder diagram is conducted under nitrogen, while maintaining the relative humidity at a level of 80-90%, The aqueous formulation so obtained is found to consist of pure hydrates of crystal form A, B, C, D. E, F or G or mixtures thereof. Example 9 Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 8 instead of the aqueous solution of sodium chloride. Example 10 400 mis of a 3.0 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (II). The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (II), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 075% by weight. The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips. Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof. Example 11 Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 10 instead of the aqueous solution of sodium chloride. Example 12 400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (I). The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (I), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight. The aqueous formulation so obtained is examined using an XPert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof. Example 13 Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 12 instead of the aqueous solution of sodium chloride. Example 14 400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (I). The temperature of the seeded solution is adjusted to 45°C,, and there are simultaneously added to the seeded solution a) a moist aqueous presscake the di-sodium salt of formula (I) (active substance content 40% by weight), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight. The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof. Example 15 400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of the di-sodium salt of formula (I). The previously-prepared batch of the di-sodium salt of formula (I) is prepared in an organic phase, containing the free acid form of the active substance, and is obtained in the last reaction step which is conducted at 90-100°C. The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution a) the said organic phase containing the free acid form of the active substance and b) water. Water and the said organic phase containing the free acid form of the active substance are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight. The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B. C, D, E, F or G or mixtures thereof. Example 16 Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 15 instead of the aqueous solution of sodium chloride. Example 17 75.0g of the free acid of 4,4'-di-triazinylamino-2,2'-di"Sulfostilbene possessing the (A) hydrate form (active content 40%) are dispersed in 24.7g of deionised water, 0.2g polysaccharide (xanthan gum type) and O.lg of Proxel GXL added and the mixture homogenised. After storing for 24 hours at 40°C or at 60°C, the mixture is neutralised with 32.8ml of 2N potassium hydroxide solution. After storing at room temperature, a readily pourable suspension of the di-potassium salt is obtained which contains 13 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 8. Example 18 75.0g of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form (active content 40%) are dispersed in 24.7g of deionised water, 0.2g polysaccharide (xanthan gum) and O.lg of Proxel GXL added and the mixture homogenised. After storing for 24 hours at 40°C, the mixture is neutralised with 32.8ml of 2N lithium hydroxide solution. After storing at room temperature, a readily pourable suspension of the di-lithium salt is obtained which contains 29 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 9. Example 19 10g of the di-lithium salt obtained as in Example 18 are stirred in a closed vessel at 60°C. After 15 minutes a clear solution results which, after prolonged stirring, then begins to reprecipitate. After stirring for 12 hours at the same temperature, the mixture is cooled and the precipitated solid filtered off. A di-lithium salt is obtained which contains 14 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 10. Example 20 Example 19 is repeated but carrying out the equilibration at a temperature of 55°C. A di-lithium salt is obtained which contains 13 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 11. Example 21 A pulp suspension of sulfite beech/spruce (50:50) is stirred in water (containing 25 ppm CaO) in the presence of 20% by weight of calcium carbonate, as filler. 0.4% by weight of each of the products of Examples 1 to 20 are added to a separate sample of the pulp suspension, and each test slurry is stirred for 15 minutes. A paper sheet is formed from each of the test pulp suspensions with an area weight of 80 g/m2, and the respective paper sheets are dried. The whiteness (CIE-Whiteness measured by SCAN-P 66:93) of each dried sheet is determined and found to be from 140-142. The CiE whiteness of paper produced in the same way but in the absence of a fluorescent whitening agent formulation according to the present invention is only 75. in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I). 2. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent sodium, the hydrates being characterised by an X-ray diffraction pattern which Is essentially as set out in the accompanying Figures 1 to 5; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di"Sulfostilbene compound having the formula (I). M and Mi representing sodium. 3. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 represent hydrogen or sodium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 6 and 7; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and M1 representing sodium. 4. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent potassium, the hydrate being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figure 8 and in which x represents 9 to 17. 5. The hydrate of the 4,4'-di'triazinylamino-2,2'-di"Sulfostilbene compound according to claim 1 in which M and M1 both represent lithium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 9 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di"triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and Mi representing lithium and in which x represents 9 to 30. 6. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent calcium or magnesium. 7. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent ammonium. 8. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as B form and characterised by an X-ray diffraction pattern which is essentially as in Figure 1. 9. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as C form and characterised by an X-ray diffraction pattern which is essentially as in Figure 2 and in which x represents 14 to 20. 10. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as D form and characterised by an X-ray diffraction pattern which is essentially as in Figure 3 and in which x represents 10 to 14. 11. A hydrate, or a mixture thereof, according to claim 2 In which the hydrate is a crystal form which is designated as E form and characterised by an X-ray diffraction pattern which is essentially as in Figure 4 and in which x represents 16 to 26. 12. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as A form and characterised by an X-ray diffraction pattern which is essentially as in Figure 5 and in which x represents 1 to 6. 13. A hydrate, or a mixture thereof, according to claim 3 in which the hydrate is a crystal form which is designated as F form and characterised by an X-ray diffraction pattern which is essentially as in Figure 6 and in which x represents 4 to 10. 14. A hydrate, or a mixture thereof, according to claim 3 in which the hydrate is a crystal form which is designated as G form and characterised by an X-ray diffraction pattern which is essentially as in Figure 7 and in which x represents 4 to 10. 15. A process for the production of the di-sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form by successively reacting cyanuric chloride with 4,4'-diaminostilbene disulphonic acid di-sodium salt, aniline and diethanolamine, adjusting the pH of the mixture to 9.0 to 9.5 with concentrated sodium hydroxide solution and evaporating the mixture to dryness. 16. A process for the production of the (C) hydrate crystal form by neutralization of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with dilute sodium hydroxide solution, homogenising and allowing to stand at room temperature; the (D) hydrate crystal form by treatment of the sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form aqueous sodium chloride solution, stabilizing and homogenising; and the (E) hydrate crystal form by treatment of the free acid of 4,4'-di-triazinylamino- 2,2'-di-sulfostilbene possessing the (A) hydrate form with concentrated sodium hydroxide solution and homogenising. 17. A process for the production of a mixture of two or more of the novel hydrates of formula (I), according to claim 2, comprises mixing an aqueous solution of an inorganic salt electrolyte and the active substance of formula (I), according to claim 2. 18. A process according to claim 17 in which the inorganic electrolyte is an alkali metal halide or sulfate. 19. A process according to claim 18 in which the alkali metal halide or sulfate is sodium chloride or sodium sulfate, or a mixture thereof. 20. A process according to any of claims 17 to 19 which comprises a) firstly preparing an aqueous solution of the electrolyte, b) seeding this electrolyte solution with a previously-prepared sample of the active substance of formula (I), obtained according to claim 17, and, while maintaining the pH value of the seeded electrolyte solution within the range of from 7.5 to 9.0, c) adding the active substance of formula (I), as the free acid, alkali, and water, simultaneously and portionwise, to the seeded electrolyte solution. 21. A process according to claim 20 in which, in step b), the pH value of the seeded electrolyte solution is maintained within the range of from 8.0 to 8.5. 22. A process according to claim 20 in which, in step c), the alkali is sodium hydroxide. 23. A process according to any of claims 17 to 22 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 5 to 40% by weight and b) the content of electrolyte in the synthesis mixture is within the range of from 0.5 to 2.5% by weight. 24. A process according to claim 23 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 10 to 30% and b) the content of electrolyte in the synthesis mixture is within the range of from 1 to 2% by weight 25. A process according to claim 23 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 15 to 25% by weight and b) the content of electrolyte in the synthesis mixture is about 1.5% by weight. 26. A process according to any of claims 15 to 25 in which the seed crystals are used in the form of small crystals whose average size does not markedly exceed 10 microns. 27. A process according to any of claims 15 to 26 in which the amount of seed crystal added is between 0.1 and 60% by weight, relative to the total active substance content. 28. A process according to claim 27 in which the amount of seed crystal added is between 1 and 50% by weight, relative to the total active substance content. 29. A process according to claim 28 in which the amount of seed crystal added is between 1 and 30% by weight, relative to the total active substance content. 30. A process according to any of claims 15 to 29 in which the reaction temperature for preparing the mixtures of hydrate of formula (I) lies within the range of from 10-95°C, 31. A process according to claim 32 in which the reaction temperature for preparing the mixtures of hydrate of formula (I) lies within the range of from 35-55°C. 32. A process for the production of the (F), form according to claim 15, in the form of the free acid, by acidifying the sodium salt of a 4,4'-di-triazinylamino-2.2'-di-sulfostilbene with hydrochloric acid and filtering the precipitated product. 33. A process for the production of compounds according to claims 4 and 5 by neutralising the free acid form of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene with potassium or lithium hydroxide, respectively. 34. An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrates (I), or a mixture thereof, as defined in claim 1. 35. An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms A, B, C, D and E of the formula (I), or a mixture thereof, as defined in claim 2. 36. An aqueous formulation according to claims 34 and 35 in which an electrolyte is also present. 37. An aqueous formulation according to claim 36 in which the electrolyte is NaCI or Na2S04, or a mixture thereof. 38. An aqueous formulation according to any of claims 34 to 37 in which one or more formulation auxiliaries selected from dispersing agents, builders, protective colloids, stabilisers, perfumes and sequestering agents are also present. 39. An aqueous formulation according to claim 40 in which the dispersing agents are anionic dispersing agents. 40. An aqueous formulation according to claim 39 in which the anionic dispersing agents are condensation products of aromatic sulfonic acids with formaldehyde, a naphthalenesulfonate or a ligninsulfonate. 41. An aqueous formulation according to claim 40 in which the condensation product of aromatic sulfonic acids with formaldehyde is a condensation product of ditolylethersulfonic acid with formaldehyde. 42. An aqueous formulation according to claim 38 in which the builders or protective colloids are modified polysaccharides derived from cellulose or heteropolysaccharides, polyvinyl alcohols (PVA), polyvinylpyrrolidones (PVP), polyethylene glycols (PEG) or aluminium silicates or magnesium silicates and are used in a concentration range of 0,01 to 2% by weight, relative to the total weight of the formulation. 43. An aqueous formulation according to claim 42 in which the modified polysaccharide derived from cellulose or heteropolysaccharides is xanthan or carboxymethylcellulose. 44. An aqueous formulation according to claim 38 in which the stabiliser is ethylene glycol or propylene glycol and is used in an amount of 0.2 to 5% by weight, relative to the total weight of the formulation. 45. An aqueous formulation according to claim 38 in which the stabiliser is 1,2-benzisothiazolin-3-one, formaldehyde or chloroacetamide and is used in an amount of 0.1 to 1% by weight, relative to the total weight of the formulation. 46. A method for the fluorescent whitening of paper or textile material, comprising contacting the paper or textile material with an aqueous formulation according to any of claims 34 to 45. 47. A method according to claim 46 in which textile material is whitened and the aqueous formulation is a detergent. 48. A method according to claim 46 or 47 in which the aqueous formulation is diluted to the optimum concentration for the practical application by the addition of further auxiliaries or water. 49, A hydrate of the 4,4' tilbene compound having the formula (I) substantialLly inbefore described with reference to the accompanying 50. A process for the of the di-sodium salt of 4,4' -di-triaziny iamino-2 , 2'-di bene subs t ant ially as hereinbefore described with e to the accompanying drawings. 51. An aqueous formulat ntially as hereinbefore described with reference to 1b ying drawings. 52, A method for the whitening of paper or textile material substant i a' inbefore described with reference to the accompanying

Full Text

The present invention relates to the novel hydrates of the salts of a specific 4.4'-di-triazinylamino-2,2'-di-sulfostilbene compound, characterised by their water of hydration content; to the crystal forms which are associated with the new hydrates and which are characterised by their X-ray diffraction pattern; to processes for the preparation of the new hydrates; and to the use of the new hydrates for the preparation of concentrated formulations of fluorescent whitening agents.
According to recent practice, fluorescent whitening agents are preferably put on the market in the form of aqueous solutions or suspensions. To this end, for example, the moist filtercakes or dry powders of the fluorescent whitening agents are suspended in water Dispersants and thickeners are added to the suspension in order to increase the homogeneity, wettability and shelf life of the suspension. Frequently, an electrolyte is also added together with these auxiliaries. Despite the presence of these additives, there are concentration limits for the fluorescent whitening agent suspension, above which the suspension is often unstable on storage and has poor metering characteristics. These concentration limits are often difficult to reproduce, since they can be affected by the nature of a pretreatment which may have been applied to the suspension of the fluorescent whitening agent. In particular, depending on the nature of a pretreatment, a variety of hydrates of the fluorescent whitening agent, having different crystal forms, may be obtained.
Surprisingly, it has now been found that formulations of a specific fluorescent whitening agent, which have an active substance concentration of more than 30% by weight, which are stable on storage and the viscosity of which can be selectively set at a value within a wide range, can be prepared if a specific hydrate or mixtures of hydrates of the fluorescent whitening agent used, having a specific crystal form, or several specific crystal forms, are present. The new formulations contain only low amounts of formulation auxiliaries and are useful for the fluorescent whitening of a wide range of substrates, including textiles and paper.

in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'"di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I).
Preferred hydrates of formula (I) are compounds in which M and Mi both represent hydrogen or sodium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 7; or a mixture containing one or more of the hydrates of the di-sodium salt of the 4,4'-di-triazinylamino-2,2'-di-suIfostiibene compound having the formula (I).
Further preferred hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound (I) are those in which M and M1 both represent potassium, the hydrate being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figure 8 and in which x represents 9 to 17 and those in which M and M1 both represent lithium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 9 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di-

triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and Mi representing lithium and in which x represents 9 to 30.
Further hydrates of interest are such hydrates of the 4,4*-di-triazinylamino-2,2'-dJ-sulfostilbene compound (I) in which M and Mi both represent calcium or magnesium and also those in which M and Mi both represent ammonium.
In compounds of formula (I) in which M and Mi both represent ammonium these may be represented by the formula -N(R)4,whereby R represents hydrogen or Cr C4-alkyl, all R-groups not necessarily being identical, or C2-C4-alkanolammonium.
The respective X-ray diffraction patterns, Figures 1 to 11, are obtained using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The reference patterns for crystal forms B (Figure 1) and C (Figure 2) are measured in suspensions in an atmosphere of air, without control of relative humidity. The measurement of the reference patterns for crystal form D (Figure 3), E (Figure 4), F (Figure 6) and G (Figure 7) and also that of the di-potassium salt (Figure 8) are also conducted in suspensions, under nitrogen, while maintaining the relative humidity at a level of 80-90%, as are those of the three crystal forms of the di-lithium salt (Figures 9-11). whilst that of crystal form A (Figure 5) was conducted in the solid state. In each of the accompanying Figures 1 to 11. there is shown the part of the measurements in the 20-area between 1* and 30°
Each of the novel hydrates of formula (I) has a characteristic X-ray diffraction pattern.
The crystal forms A, B, C, D, E, F and G and also those of the di-potassium and lithium salts consist for the most part of one or more hydrates of the formula (I) in which X is a number between 1 and 30.
The amount of water of hydration may be determined via
. differential thermal analysis or dynamic differential calorimetry in which the proportion of the unbound water, that is the water melting at 0°C, is

measured, or by subsequent water analysis by methods such as Karl Fischer titration, thermogravimetric analysis or loss on drying at elevated temperature.
The di-sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form may be produced by successively reacting cyanuric chloride with 4,4'-diaminostiibene disulphonic acid di-sodium salt, aniline and diethanoiamine, adjusting the pH of the mixture to 9.0 to 9.5 with concentrated sodium hydroxide solution and evaporating the mixture to dryness. If, prior to treatment with sodium hydroxide, the compound is isolated in the form of the free acid, a hydrate results possessing the (F) crystal form.
The (C) hydrate crystal form may be obtained by neutralization of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with dilute sodium hydroxide solution, homogenising and allowing to stand at room temperature; the (D) hydrate crystal form by treatment of the sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form aqueous sodium chloride solution, stabilizing and homogenising; and the (E) hydrate crystal form by treatment of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with concentrated sodium hydroxide solution and homogenising. The (G) crystal form of the hydrate may be obtained from the (E) form by equilibration in a closed vessel at elevated temperature.
The (C) hydrate can further be prepared by seeding an aqueous suspension of the corresponding free acid, with (C) seed crystals. This technique has the advantage that active substance concentrations of more than 30% by weight, preferably 30 to 50% by weight, can be used and thus the suspension obtained is formed in the desired concentration and does not have to be concentrated.
The hydrate of crystal form (D) in accordance with Figure 3, or the hydrate of crystal form which is designated as (E) form and characterised by an X-ray diffraction pattern which is essentially as in Figure 4, may also be prepared by the seeding technique described in relation to the production of the (C) form.

In a preferred embodiment, a mixture of one or more of the novel hydrates of formula (I) is prepared by the controlled mixing of an aqueous solution of an inorganic salt electrolyte, preferably an alkali metal halide or sulfate, especially sodium chloride or sodium sulfate; and the active substance of formula (I). The process is conveniently conducted by firstly preparing an aqueous solution of the electrolyte and then seeding this electrolyte solution with a previously-prepared sample of the active substance of formula (I). While maintaining the pH value of the seeded electrolyte solution within the range of from 7.5 to 9.0, preferably from 8.0 to 8.5, active substance of formula (I), as the free acid, alkali, preferably sodium hydroxide and water are preferably added, simultaneously and portionwise, to the seeded electrolyte solution. Preferably, water and the free acid form of the active substance are added until a) the content of the active substance in the synthesis mixture is within the range of from 5 to 40%, preferably from 10 to 30% and especially from 15 to 25% by weight and b) the content of electrolyte in the synthesis mixture is within the range of from 0.5 to 2.5%, preferably from 1 to 2% and especially about 1.5% by weight.
The seed crystals should be used in the form of small crystals whose average size does not markedly exceed 10 micron. This allows the substantial reduction of the seed crystal content, for example down to 0.1 to 5% by weight, relative to the total active substance content. The seeding is preferably effected without stirring.
The seed crystal content is in general between 0.1 and 60% by weight, preferably between 1 and 50% by weight, and particulariy preferably between 1 and 30% by weight, relative to the total active substance content. In all cases in which only a portion of the final compound is replaced by new starting material, the conversion can be carried out as semi-continuous or continuous process.
The reaction temperature for preparing the mixtures of hydrate of formula (I) according to the present invention preferably lies within the range of from 10-95°C and preferably within the range of from 35-55°C.
The di-potassium and lithium salts of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene (I) may be obtained by neutralising the free acid form of 4,4'-di-triazinylamino-2,2'-di-

sulfostilbene with potassium or lithium hydroxide, respectively. In the case of the di-lithium salt, two further crystal forms of the hydrates may be obtained by equilibrating a slurry of the salt obtained directly by neutralisation at elevated temperatures.
The invention also provides an aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms of the formula (I). This formulation remains flowable, has good metering characteristics and is stable for months, without forming sediments, even after standing at temperatures of between 5-40°C for an extended period of time.
An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms A, B, C, D, E, F and G of the formula (I) is highly viscous when no formulation auxiliaries are added and is suitable for the production of brushable pastes or for being incorporated therein.
Thus, by incorporating the active substance in the form of one or more of novel hydrate forms of the formula (I) having different crystal forms, a desired viscosity of an aqueous formulation can be selectively established, without the presence of any further auxiliaries. An electrolyte, for example NaCI or Na2S04, or a mixture thereof, can be admixed with the aqueous formulation in order to stabilise the hydrates contained therein.
A particular advantage of the hydrates according to the present invention having different crystal forms is that they enable ready-to-use and stable formulations of a wide range of viscosities to be produced, without addition of ecologically harmful formulation auxiliaries.
If desired, however, the formulations obtained according to the present invention may contain customary formulation auxiliaries, such as dispersing agents, builders, protective colloids, stabilisers, preservatives, perfumes and sequestering agents.

Dispersing agents are preferably anionic dispersing agents, such as condensation products of aromatic sulfonic acids with formaldehyde, for example ditolylethersulfonic acid, a naphthalenesulfonate or a ligninsulfonate.
Examples of suitable builders or protective colloids are modified polysaccharides derived from cellulose or heteropolysaccharides, such as xanthan, carboxymethylcellulose and polyvinyl alcohols (PVA), polyvinylpyrrolidones (PVP), polyethylene glycols (PEG) and aluminium silicates or magnesium silicates. They are usually used in a concentration range of 0.01 to 2% by weight and preferably 0.05 to 0.5% by weight, relative to the total weight of the formulation.
Examples of auxiliaries which can be used for stabilisation are ethylene glycol, propylene glycol or dispersants in an amount of 0.2 to 5% by weight and preferably 0.3 to 2% by eight, relative to the total weight of the formulation.
Compounds which may be used as stabilisers include 1,2-benzisothiazolin-3-one, formaldehyde or chloroacetamide in an amount of 0.1 to 1% by weight and preferably 0.1 to 0,5% by weight relative to the total weight of the formulation.
The concentrated formulation thus prepared can be used for the fluorescent whitening of paper or textile material, for example in detergents. To this end, they are in general diluted to the optimum concentration for the practical application by the addition of further auxiliaries or water.
The following Examples further illustrate the present invention. Parts and percentages shown therein are by weight unless otherwise stated.
Example 1
In a reaction vessel, 400g of ice, 120g of cyanuric chloride and 785g of methyl ethyl ketone are mixed and, with intensive stirring and external cooling, treated with a solution of 120g of 4,4'-diaminostilbene-2,2'-disulphonic acid disodium salt in 800g of water and 164.5g of 17% sodium carbonate solution over 20 minutes at 5-10°C, the pH being maintained at 4.5 by the simultaneous addition of 39.4g of

17% sodium carbonate solution. After the addition, 55.4g of aniline and 8,7g of diethanolamine are added, the pH being maintained at 7.5 by the simultaneous addition of 72.2g of 36% sodium hydroxide solution. After heating to 60°C, 78.8g of diethanolamine are added whilst maintaining the pH at 8.2 by the simultaneous addition of 72.2g of 36% sodium hydroxide solution. The reaction mixture is heated to reflux and the methyl ethyl ketone destilled off, being gradually replaced by 1000g of water. At a temperature of 95°C, the mixture is acidified to pH 4.5 by the addition of 170g of 16% hydrochloric acid solution and the volume adjusted to 2.71 by addition of water. After cooling to 70°C, the mixture is filtered and the filter cake washed with 1.81 of water to yield the free acid. A 30% aqueous suspension of this free acid is heated to 95°C and the pH adjusted to 9.0-9.5 by the addition of 36% sodium hydroxide solution. The resulting solution is then evaporated to dryness to yield a compound of Formula (1) as the di-sodium salt, which has the A-crystal form containing 1 mole of water, corresponding to the X-ray diffraction pattern which is set out in the accompanying Figure 5.
Example 2
75.0 g of the free acid form (having an active substance content of 40% by weight) of the di-sodium salt of formula (I) are dispersed in 24.7 g of deionised water at 25°'C. The dispersion so obtained is stabilised by adding to it 0.2 g of xanthan gum and 0.1 g of Proxe! GXL (1,2-benzisothiazolin"3-one) and the mixture is homogenised. The homogenised suspension is neutralised with 32.8 mis of a 2N aqueous sodium hydroxide solution. The homogenised, neutralised suspension has the B-crystal form which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 1.
After standing for two days at 25°C., a suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 2.

Using the same procedure, but using, as starting material, the di-sodium salt of formula (I) in the form of a pure hydrate of the A, B, D, E, F or G crystal form, or a mixture thereof, a suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water, which corresponds to the X-ray diffraction pattern which (s set out in the accompanying Figure 2.
Example 3
700g of the moist filter cake from Example 1 (= 265g of free acid) are gradually added to 314g of water at 40-45°C whilst maintaining the pH at 8 J-9.1 by the simultaneous addition of 64g of 36% sodium hydroxide solution. Then, at 42°C. 20g of seed crystals of the C form of the hydrate obtained in Example 2 are added. After 5 hours, the liquid dispersion is cooled to 25-30°C and stabilised by the addition of 2.2g of 50% glutaraldehyde solution and 2.2g of xanthan gum (polysaccharide), predispersed in 5.5g of propylene glycol. A liquid suspension is obtained which is readily pourable and which has the C-crystal form containing 17 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 2.'
Example 4
In a reaction flask, 400 g of a 6% aqueous sodium chloride solution are preheated to 60°C. Into this solution are introduced 120 g of the di-sodium salt of formula (I) (having an active substance content of 90% by weight and containing 10% sodium chloride) and the mixture is heated to 90°C. 180 g of 6% aqueous sodium chloride solution are added and the mixture is cooled, with stirring, to 25°C, The resulting liquid suspension is stabilised by the addition of 2.45 g of xanthan gum which has been pre-dispersed in 6.1 g of 1,2-propylene glycol and the mixture is heated to 90°C. for two hours. The mixture is cooled, with stirring, to 25°C., 3.22 g of Proxel GXL (1,2-benzisothiazolin-3-one) are added, as stabiliser, the mixture is stirred for a further twelve hours and finally homogenised using a high speed stirrer A suspension is obtained which has the D-crystal form containing 14 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 3.

Example 5
In a reaction flask, 400 mis of deionised water are pre-heated to 40°C. Into this water are introduced, portionwise, 800 g of the free acid form (having an active substance content of 40% by weight) of the di-sodium salt of formula (I) and, by the simultaneous portionwise addition of 50.45 mis of a 37% (50% g/v %) aqueous sodium hydroxide solution, the pH value of the mixture is kept constant at 8.2. After the addition is complete, the whole is diluted with 400 mis of deionised water, stirred for one hour and then homogenised. A suspension is obtained which has the E-crystal form containing 14 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 4.
Example 6
620g of the moist filter cake obtained as in Example 1 (= 279g free acid) are dispersed in 304g of water and stabilised by the addition of 1.7g of Proxel GXL and 1.7g of xanthan gum (polysaccharide), predispersed in 3.3g of propylene glycol. A liquid suspension is obtained which has the F crystal form containing 7 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 6.
Example 7
A 20% slurry of the E crystal form of the hydrate, obtained as in Example 5, is stirred in a closed vessel at 60°C and maintained at this temperature for at least 20 hours. After cooling to room temperature, a liquid suspension is obtained which has the G crystal form containing 7 moles of water, which corresponds to the X-ray diffraction pattern which is set out in the accompanying Figure 7.
Example 8
400 mis of a 6.0 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (II). The temperature of the seeded solution is

adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (II), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 1.5% by weight.
The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The device is fitted with a closed sample chamber (Anton Parr) which can be adapted to be purged with gas. The aqueous formulation is filled tel quel into the sample carrier (layer thickness 0.8 mm) and the measurement of the powder diagram is conducted under nitrogen, while maintaining the relative humidity at a level of 80-90%, The aqueous formulation so obtained is found to consist of pure hydrates of crystal form A, B, C, D. E, F or G or mixtures thereof.
Example 9
Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 8 instead of the aqueous solution of sodium chloride.
Example 10
400 mis of a 3.0 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (II). The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (II), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at

8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 075% by weight.
The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips. Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof.
Example 11
Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 10 instead of the aqueous solution of sodium chloride.
Example 12
400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (I). The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution, a) a moist aqueous presscake of the free acid form (active substance content 40% by weight) of the di-sodium salt of formula (I), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight.
The aqueous formulation so obtained is examined using an XPert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof.

Example 13
Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 12 instead of the aqueous solution of sodium chloride.
Example 14
400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of an aqueous slurry of the di-sodium salt of formula (I). The temperature of the seeded solution is adjusted to 45°C,, and there are simultaneously added to the seeded solution a) a moist aqueous presscake the di-sodium salt of formula (I) (active substance content 40% by weight), b) aqueous sodium hydroxide solution and c) water, while maintaining the pH value of the resulting mixture constant at 8.2. Water and the moist aqueous presscake of the free acid form are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight.
The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B, C, D, E, F or G or mixtures thereof.
Example 15
400 mis of a 1.5 % by weight aqueous sodium chloride solution are prepared. This solution is then seeded with a previously-prepared batch of the di-sodium salt of formula (I). The previously-prepared batch of the di-sodium salt of formula (I) is prepared in an organic phase, containing the free acid form of the active substance, and is obtained in the last reaction step which is conducted at 90-100°C. The temperature of the seeded solution is adjusted to 45°C., and there are simultaneously added to the seeded solution a) the said organic phase containing

the free acid form of the active substance and b) water. Water and the said organic phase containing the free acid form of the active substance are added until the content of active substance of the free acid form in the reaction mixture is within the range of from 15 to 25% by weight and the content of sodium chloride in the reaction mixture is 0.25% by weight.
The aqueous formulation so obtained is examined using an X'Pert powder diffractometer (Philips, Almelo) in reflexion geometry and Cu radiation. The aqueous formulation so obtained is found to be a pure hydrate of crystal form A, B. C, D, E, F or G or mixtures thereof.
Example 16
Similar results are obtained when an aqueous solution of sodium sulfate is used as starting material in Example 15 instead of the aqueous solution of sodium chloride.
Example 17
75.0g of the free acid of 4,4'-di-triazinylamino-2,2'-di"Sulfostilbene possessing the (A) hydrate form (active content 40%) are dispersed in 24.7g of deionised water, 0.2g polysaccharide (xanthan gum type) and O.lg of Proxel GXL added and the mixture homogenised. After storing for 24 hours at 40°C or at 60°C, the mixture is neutralised with 32.8ml of 2N potassium hydroxide solution. After storing at room temperature, a readily pourable suspension of the di-potassium salt is obtained which contains 13 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 8.
Example 18
75.0g of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form (active content 40%) are dispersed in 24.7g of deionised water, 0.2g polysaccharide (xanthan gum) and O.lg of Proxel GXL added and the

mixture homogenised. After storing for 24 hours at 40°C, the mixture is neutralised with 32.8ml of 2N lithium hydroxide solution.
After storing at room temperature, a readily pourable suspension of the di-lithium salt is obtained which contains 29 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 9.
Example 19
10g of the di-lithium salt obtained as in Example 18 are stirred in a closed vessel at 60°C. After 15 minutes a clear solution results which, after prolonged stirring, then begins to reprecipitate. After stirring for 12 hours at the same temperature, the mixture is cooled and the precipitated solid filtered off. A di-lithium salt is obtained which contains 14 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 10.
Example 20
Example 19 is repeated but carrying out the equilibration at a temperature of 55°C. A di-lithium salt is obtained which contains 13 moles of water, characterised by an X-ray diffraction pattern which is shown in Figure 11.
Example 21
A pulp suspension of sulfite beech/spruce (50:50) is stirred in water (containing 25 ppm CaO) in the presence of 20% by weight of calcium carbonate, as filler.
0.4% by weight of each of the products of Examples 1 to 20 are added to a separate sample of the pulp suspension, and each test slurry is stirred for 15 minutes. A paper sheet is formed from each of the test pulp suspensions with an area weight of 80 g/m2, and the respective paper sheets are dried. The whiteness (CIE-Whiteness measured by SCAN-P 66:93) of each dried sheet is determined and found to be from 140-142. The CiE whiteness of paper produced in the same way but in the absence of a fluorescent whitening agent formulation according to the present invention is only 75.

in which M and M1 independently represent hydrogen, an alkaline-, an alkaline earth metal or ammonium, x is a number within the range of from 1 to 30, and the crystal form of the hydrate (I) being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 1 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I).
2. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound
according to claim 1 in which M and M1 both represent sodium, the hydrates being
characterised by an X-ray diffraction pattern which Is essentially as set out in the
accompanying Figures 1 to 5; or a mixture containing one or more of the hydrates
of the 4,4'-di-triazinylamino-2,2'-di"Sulfostilbene compound having the formula (I).
M and Mi representing sodium.
3. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound
according to claim 1 in which M and M1 represent hydrogen or sodium, the
hydrates being characterised by an X-ray diffraction pattern which is essentially as
set out in the accompanying Figures 6 and 7; or a mixture containing one or more

of the hydrates of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and M1 representing sodium.
4. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent potassium, the hydrate being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figure 8 and in which x represents 9 to 17.
5. The hydrate of the 4,4'-di'triazinylamino-2,2'-di"Sulfostilbene compound according to claim 1 in which M and M1 both represent lithium, the hydrates being characterised by an X-ray diffraction pattern which is essentially as set out in the accompanying Figures 9 to 11; or a mixture containing one or more of the hydrates of the 4,4'-di"triazinylamino-2,2'-di-sulfostilbene compound having the formula (I), M and Mi representing lithium and in which x represents 9 to 30.
6. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent calcium or magnesium.
7. The hydrate of the 4,4'-di-triazinylamino-2,2'-di-sulfostilbene compound according to claim 1 in which M and M1 both represent ammonium.
8. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as B form and characterised by an X-ray diffraction pattern which is essentially as in Figure 1.
9. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as C form and characterised by an X-ray diffraction pattern which is essentially as in Figure 2 and in which x represents 14
to 20.
10. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a
crystal form which is designated as D form and characterised by an X-ray
diffraction pattern which is essentially as in Figure 3 and in which x represents 10
to 14.

11. A hydrate, or a mixture thereof, according to claim 2 In which the hydrate is a crystal form which is designated as E form and characterised by an X-ray diffraction pattern which is essentially as in Figure 4 and in which x represents 16 to 26.
12. A hydrate, or a mixture thereof, according to claim 2 in which the hydrate is a crystal form which is designated as A form and characterised by an X-ray diffraction pattern which is essentially as in Figure 5 and in which x represents 1 to 6.
13. A hydrate, or a mixture thereof, according to claim 3 in which the hydrate is a crystal form which is designated as F form and characterised by an X-ray diffraction pattern which is essentially as in Figure 6 and in which x represents 4 to 10.
14. A hydrate, or a mixture thereof, according to claim 3 in which the hydrate is a crystal form which is designated as G form and characterised by an X-ray diffraction pattern which is essentially as in Figure 7 and in which x represents 4 to 10.
15. A process for the production of the di-sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form by successively reacting cyanuric chloride with 4,4'-diaminostilbene disulphonic acid di-sodium salt, aniline and diethanolamine, adjusting the pH of the mixture to 9.0 to 9.5 with concentrated sodium hydroxide solution and evaporating the mixture to dryness.
16. A process for the production of the (C) hydrate crystal form by neutralization of the free acid of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form with dilute sodium hydroxide solution, homogenising and allowing to stand at room temperature; the (D) hydrate crystal form by treatment of the sodium salt of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene possessing the (A) hydrate form aqueous sodium chloride solution, stabilizing and homogenising; and the (E) hydrate crystal form by treatment of the free acid of 4,4'-di-triazinylamino-

2,2'-di-sulfostilbene possessing the (A) hydrate form with concentrated sodium hydroxide solution and homogenising.
17. A process for the production of a mixture of two or more of the novel hydrates of formula (I), according to claim 2, comprises mixing an aqueous solution of an inorganic salt electrolyte and the active substance of formula (I), according to claim 2.
18. A process according to claim 17 in which the inorganic electrolyte is an alkali metal halide or sulfate.
19. A process according to claim 18 in which the alkali metal halide or sulfate is sodium chloride or sodium sulfate, or a mixture thereof.
20. A process according to any of claims 17 to 19 which comprises a) firstly preparing an aqueous solution of the electrolyte, b) seeding this electrolyte solution with a previously-prepared sample of the active substance of formula (I), obtained according to claim 17, and, while maintaining the pH value of the seeded electrolyte solution within the range of from 7.5 to 9.0, c) adding the active substance of formula (I), as the free acid, alkali, and water, simultaneously and portionwise, to the seeded electrolyte solution.
21. A process according to claim 20 in which, in step b), the pH value of the seeded electrolyte solution is maintained within the range of from 8.0 to 8.5.
22. A process according to claim 20 in which, in step c), the alkali is sodium hydroxide.
23. A process according to any of claims 17 to 22 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 5 to 40% by weight and b) the content of electrolyte in the synthesis mixture is within the range of from 0.5 to 2.5% by weight.

24. A process according to claim 23 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 10 to 30% and b) the content of electrolyte in the synthesis mixture is within the range of from 1 to 2% by weight
25. A process according to claim 23 in which water and the free acid form of the active substance are mixed until a) the content of the active substance in the synthesis mixture is within the range of from 15 to 25% by weight and b) the content of electrolyte in the synthesis mixture is about 1.5% by weight.
26. A process according to any of claims 15 to 25 in which the seed crystals are used in the form of small crystals whose average size does not markedly exceed 10 microns.
27. A process according to any of claims 15 to 26 in which the amount of seed crystal added is between 0.1 and 60% by weight, relative to the total active substance content.
28. A process according to claim 27 in which the amount of seed crystal added is between 1 and 50% by weight, relative to the total active substance content.
29. A process according to claim 28 in which the amount of seed crystal added is between 1 and 30% by weight, relative to the total active substance content.
30. A process according to any of claims 15 to 29 in which the reaction temperature for preparing the mixtures of hydrate of formula (I) lies within the range of from 10-95°C,
31. A process according to claim 32 in which the reaction temperature for preparing the mixtures of hydrate of formula (I) lies within the range of from 35-55°C.

32. A process for the production of the (F), form according to claim 15, in the form of the free acid, by acidifying the sodium salt of a 4,4'-di-triazinylamino-2.2'-di-sulfostilbene with hydrochloric acid and filtering the precipitated product.
33. A process for the production of compounds according to claims 4 and 5 by neutralising the free acid form of 4,4'-di-triazinylamino-2,2'-di-sulfostilbene with potassium or lithium hydroxide, respectively.
34. An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrates (I), or a mixture thereof, as defined in claim 1.
35. An aqueous formulation containing 30-50% by weight of active substance in the form of one or more of novel hydrate forms A, B, C, D and E of the formula (I), or a mixture thereof, as defined in claim 2.
36. An aqueous formulation according to claims 34 and 35 in which an electrolyte is also present.
37. An aqueous formulation according to claim 36 in which the electrolyte is NaCI or Na2S04, or a mixture thereof.
38. An aqueous formulation according to any of claims 34 to 37 in which one or more formulation auxiliaries selected from dispersing agents, builders, protective colloids, stabilisers, perfumes and sequestering agents are also present.
39. An aqueous formulation according to claim 40 in which the dispersing agents are anionic dispersing agents.
40. An aqueous formulation according to claim 39 in which the anionic dispersing agents are condensation products of aromatic sulfonic acids with formaldehyde, a naphthalenesulfonate or a ligninsulfonate.

41. An aqueous formulation according to claim 40 in which the condensation product of aromatic sulfonic acids with formaldehyde is a condensation product of ditolylethersulfonic acid with formaldehyde.
42. An aqueous formulation according to claim 38 in which the builders or protective colloids are modified polysaccharides derived from cellulose or heteropolysaccharides, polyvinyl alcohols (PVA), polyvinylpyrrolidones (PVP), polyethylene glycols (PEG) or aluminium silicates or magnesium silicates and are used in a concentration range of 0,01 to 2% by weight, relative to the total weight of the formulation.
43. An aqueous formulation according to claim 42 in which the modified polysaccharide derived from cellulose or heteropolysaccharides is xanthan or carboxymethylcellulose.
44. An aqueous formulation according to claim 38 in which the stabiliser is ethylene glycol or propylene glycol and is used in an amount of 0.2 to 5% by weight, relative to the total weight of the formulation.
45. An aqueous formulation according to claim 38 in which the stabiliser is 1,2-benzisothiazolin-3-one, formaldehyde or chloroacetamide and is used in an amount of 0.1 to 1% by weight, relative to the total weight of the formulation.
46. A method for the fluorescent whitening of paper or textile material, comprising contacting the paper or textile material with an aqueous formulation according to any of claims 34 to 45.
47. A method according to claim 46 in which textile material is whitened and the aqueous formulation is a detergent.
48. A method according to claim 46 or 47 in which the aqueous formulation is diluted to the optimum concentration for the practical application by the addition of further auxiliaries or water.

49, A hydrate of the 4,4' tilbene compound having
the formula (I) substantialLly inbefore described with
reference to the accompanying
50. A process for the of the di-sodium salt of
4,4' -di-triaziny iamino-2 , 2'-di bene subs t ant ially as
hereinbefore described with e to the accompanying
drawings.
51. An aqueous formulat ntially as hereinbefore
described with reference to 1b ying drawings.
52, A method for the whitening of paper or
textile material substant i a' inbefore described with
reference to the accompanying

Documents:

1095-mas-1998-abstract.pdf

1095-mas-1998-claims filed.pdf

1095-mas-1998-claims granted.pdf

1095-mas-1998-correspondnece-others.pdf

1095-mas-1998-correspondnece-po.pdf

1095-mas-1998-description(complete)filed.pdf

1095-mas-1998-description(complete)granted.pdf

1095-mas-1998-drawings.pdf

1095-mas-1998-form 1.pdf

1095-mas-1998-form 26.pdf

1095-mas-1998-form 3.pdf

1095-mas-1998-form 4.pdf

1095-mas-1998-form 5.pdf

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Patent Number

212412

Indian Patent Application Number

1095/MAS/1998

PG Journal Number

07/2008

Publication Date

15-Feb-2008

Grant Date

03-Dec-2007

Date of Filing

22-May-1998

Name of Patentee

CIBA SPECIALTY CHEMICALS HOLDING INC

Applicant Address

KLYBECKSTRASSE 141 4057 BASEL,

Inventors:

#	Inventor's Name	Inventor's Address
1	PETER ROHRINGER	SECHSJUCHARTENSTRASSE 1, 4124 SCHONENBUCH,
2	ANDRE GEOFFROY	RUE ST.MARTIN 23, 68440 HABSHEIM,
3	ANDREAS BURKHARD	BLOTZHEIMERSTRASSE 29, 4055 BASEL,
4	ERWIN MARTI	IM LANGEN LOH 181, 4054 BASEL,
5	WERNER SCHREIBER	RIEHENSTRASSE 264, 4058 BASEL,
6	JOSEF ZELGER	PARADIESSTRASSE 1, 4125 RIEHEN,

PCT International Classification Number

C 07 D 251/68

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	9710569.6	1997-05-23	U.K.