Title of Invention

A DETERGENT COMPOSITION

Abstract An oleo-pneumatic shock absorber for land vehicles that consists of a twin tube comprising an outer tube housing an inner tube. A canister is attached to the outer tube at its bottom end. The inner tube is fitted with a base valve and has got inserted in it a piston rod fitted with a piston. The top open end of the outer tube is sealed with a sealing device including a seal shield. A collapsible chamber having a cap is provided inside the canister. A hollow screw having a seal at its one end and female threads at its other end is provided on the cap, another screw with male threads is provided to engage the female threads on the hollow screw. The collapsible chamber inserted in the canister is sealed with a circlip.
Full Text 1 3 DEC 2004
FORM-2
THE PATENTS ACT, 1970
(39 OF 1970)
COMPLETE SPECIFICATION
(SECTION 10)
AN IMPROVED OLEO-PNEUMATIC SHOC1
VEHICLES AND THE I
ENDURANCE SYSTEMS (INDIA) PRIVATE LIMITED, a Company incorporated under the Indian Companies Act, 1956, of E-92, M.I.D.C Industrial Area, Waluj, Aurangabad - 431 136, in the State of Maharashtra, India.
The following specification describes the nature of this invention and the manner in which it is to be performed :-
13 DEC2004

Field of invention
The present invention relates synthetic detergent compositions, especially but not limited to personal wash products. In particular, the invention relates to a synthetic detergent personal wash product comprising a novel binder/structarant which effectively provides thermoplastic properties to synthetic surfactants without compromising on mildness, lather, cost etc and results in improved toilet preparations with enhanced foamability, rinsability, lather and mush.
Background of the invention
The soaps are the oldest known surfactants and are extensively used for cleaning applications, especially body wash, personal hygiene etc. Over the last few decades the art of manufacturing personal washing bars have progressed to satisfy different, increasing needs of the consumer. Mildness is one such important need of the consumer. This is followed by improvement with respect to hardness tolerance by using synthetic surfactants.
There are two broad approaches followed to make mild soap. According to the first approach common fatty acid soaps are employed as primary ingredients and mildness increased with additives and secondary surfactants.
The second approach is more sophisticated as it employs major non-soap surfactants, with proven mildness to the skin.
Among the several surfactants being used in detergent bars for end use in toilet bathing bar the prominent are fatty alcohol sulfate,fatty alcohol ethoxylates, fatty alcohol ether sulphate,
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linear alkyl benzene sulphonate, alkyl monoethanolamide, alkyl amidopropyl betaine, alkyl sulphosuccinates, isethionates etc.
Several prior art viz. EP 363215, EP 537964, US 5296159 disclose detergent preparations comprising one or many of the above mentioned surfactants.
Despite overwhelmingly better performance for usage in personal
care, synthetic detergent or combination bar have not replaced
soap for many reasons. Primary among them is poor physical
characteristic of synthetic detergent bars.
The alkyl isethionates, sodium fatty alcohol sulphate and alkyl sulphosuccinates are three largely used surfactant for synthetic detergents bathing preparations, alone or in combination using various process aids. Isethionates satisfy requirement of plasticity only to certain extent as compared to soaps. The above mentioned synthetic surfactants lack suitable thermoplastic properties. This limits their usage in the art of soap making as primary surfactant. Thus binders/structurants are required. The same should allow efficient bar manufacturing. In addition, the binder should impart smooth sensory properties to the composition.
The following US patents teach binders and proportions thereof in mild detergent formulations involving synthetic detergents mentioned above.
US 2781321 relates to a detergent bar having superior user properties and comprises as a major detergent an acyl isethionate and supplemental detergent binder and plastisizer components. The prior art discloses, as a component of the bar composition, a synthetic organic anionic lathering agent
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selected from the group consisting of a water soluble alkali metal and amine salts of an alkylaryl sulfonate containing at least 1 alkyl side chain radical of from 2 to 6 carbon atoms and devoid of alkyl side chain radicals of more than 6 carbon atoms and a synthetic organic anionic lathering agent selected from the group consisting of a water soluble alkali metal and amine salts of a lower alkyl ester of a lower aliphatic sulphopolycarboxyl acid containing an open chain of from 3 to 9 carbon atoms.
US 2894912 relates to the production of an all purpose detergent bar or cake suitable for use in soft water, hard water and sea water. This prior art discloses, as part of detergent bar composition, at least one higher fatty acid having from about 12 to about 25 carbon atoms as binder and plasticiser.
US 4234464 discloses a detergent bar binder comprising (i) fatty acid or alcohol component having an iodine number less than about 20 and a melting point of at least about 50°C and selected from the group consisting of fatty acids or alcohols having from 12 to 22 carbon atoms, mono-, di- or triglycerides of such fatty acids, fatty acid esters of such fatty alcohols and mixtures thereof and (ii) alkyl amide represented by a given formula. Such binder is used in a non-soap detergent bar containing anionic foaming and foam boosting detergents.
US 6384000 discloses bars and process for making bars comprising synthetic anionic, fatty acid soap and hydroxy acid salt wherein bar can be extruded at minimum rates and wherein the bar and process are defined by specified ratio of hydroxy acid salt to calcite filler. The bar composition comprises (a) 10 to 50% by
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wt. anionic surfactant; (b) 5 to 30% by wt. fatty acid soap; (c) 2 to 20% hydroxy acid salt; wherein bar is extruded at rate of at least 150 grams/minute in a laboratory scale extruder; wherein the bar comprises sufficient calcite filler such that ratio of calcite filler to hydroxy acid salt is above about 0.75:1 to about 2:1; and wherein ratio of anionic to soap is greater than 1:1.
Generally, an al0yl isethionate is used as primary surfactant along with some secondary surfactants. Several types of process aids and structurants/binders have been suggested along with other performance enhancing agents such as cationic polymers.
Long chain fatty acids mainly stearic acid, palmitic acid, paraffin wax, cetostearyl alcohol fatty acid soap, fatty acid amide of alkanol amines are some of the binder used for this purpose, as disclosed in prior art.
The known binders have several disadvantages. They depress the foamability of the detergent bar and to achieve foamability similar to fatty acid soaps and thus require more active matter and in turn more binder/structurant. Moreover, if 10% to 15% of fatty acid soaps are used as binder in such formulations, the pH of the bar increases beyond the pH range of 5.5 to 6.5, which is actual skin compatible pH range. Although the binders are added to compositions in small quantities, the products become harsh for the skin. Consequently, as a pH balancing component fatty acids have to be introduced in such formulations which can bring the pH to around 7.0. But the quantities of fatty acids so used have dampening effect on foaming and rinsability of the product. The foam dampening effect requires increased use of surfactant
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and thus the cost increases. Additionally, oily residue left on the skin due to use of fatty acids in synthetic detergent based bars give uneasy feeling to user. Possibility of getting skin pore clogs is also apprehended.
In view of prior art, it will be appreciated that while making synthetic detergent bars some degree of compromise is made by using component detrimental to over all performance. For example excess of surfactant is used to overcome depression of foam /lather due to usage of binders such as fatty acid or triglyceride. Soap is used as plasticising agent, in many cases from 5 to 30% or more. Thus mildness is compromised. Soap also pushes the pH above the skin friendly pH range of 6.0 to 6.5.
Objects of the invention
Thus the object of the present invention is to provide synthetic detergent bar compositions that have enhanced thermoplastic properties while having superior foamability. Thermoplasticity is a property of the material due to which the material can be drawn in to solid homogeneous bars of suitable shape and sizes using extrusion machines. These bars can be subsequently converted in to pieces of different shape using stamping machine. A good thermo plastic material retains homogeneity and shape on cooling, storage without deshaping or cracking after cooling or ageing.
Another object of the present invention is to provide synthetic detergent bar compositions with no soap content, even in smaller quantities, thus avoiding harshness imparted by soap resulting in milder bath preparations.
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Yet another object of the present invention is to provide synthetic detergent bar compositions which do not contain fatty acids, paraffin wax, fatty alcohol.
A further object of the present invention is to provide synthetic detergent bar compositions possessing better foamability at lower level of actives in the preparations.
A yet further object of the present invention is to provide synthetic detergent bar compositions having attributes provided in the earlier objects having a pH which remains within the skin pH range of 5.5 to 6.5.
Summary of the invention
Thus according to the present invention there is provided a synthetic detergent composition comprising a binder/structurant compound of formula 1 or mixtures thereof
R1CO -N(H)Z -((CH2CH20 - (CH2CH20)n)x - CO - R2)Y (I)
wherein, Ri and R2 are alkyl groups, and selected from 6 to 20
carbon atoms;
n = 0 to 10;
x = 1 to 10; y = 1 or 2 and Z = 0 or 1
wherein when y = 1, then z = 1 and when y = 2, then z = 0.
According to a preferred aspect of the present invention, y = 1 and z = 1 such that the compound of formula 1 is a compound of formula 2.
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Rl — CO - NH - CH2CH20 - ( (CH2CH20) n) X — CO — R2 (2)
wherein Ri, R2# n and x are same as defined in formula 1. According to another preferred aspect of the present invention, y = 2 and z = 0 such that the compound of formula 1 is a compound of formula 3.
Rl — CO ~ N — ( (CH2CH20 — {CH2CH20)n)x - CO - R2)2 (3)
wherein Rlf R2 n and x are same as defined in formula 1. Detailed description
The applicants have surprisingly found that compounds of formula 1, 2 and 3 act as an efficient binder/structurant in a detergent composition and are prepared using conventional amidification and esterification reactions. The compounds of formula 1, 2 and 3 are amide esters and are prepared using available commercial quality of alkanol amides and fatty acids. Alkanol amides may be prepared in accordance with step 1 described below or obtained from other sources. In step 2 the amide is reacted with desired fatty acid to get the amide ester compound.
Step 1: Preparation of alkanol amide:
In a round bottom flask, the desired fatty acid and alkanol amine is taken. The same is heated to melt with nitrogen purging. The temperature is increased to 100 degree with constant stirring and vacuum of about 100 to 300 mm of Hg. The
... page 8

temperature is increased to 120 degree centigrade. The reaction mass is digested at temperature between 120 to 200, preferably between 150 to 175 degree for several hours. The reaction is controlled by acid value analysis of the reaction mass. After getting Acid value of less than 5.0, preferably less than 3 the product is poured in to trays to get solid flakes/briquettes.
Step 2: Preparation of amide ester
In a round bottom flask, the fatty acid alkanol amide is taken. The same is heated to melt with nitrogen purging. The temperature is increased to 100 degree. The fatty acid is added to the molten mass with increase in temperature. With constant stirring, temperature is increased to 120 degree centigrade. The reaction mass is digested at temperature between 120 to 200, preferably between 150 to 175 degree for several hours. The reaction is controlled by acid value analysis of the reaction mass. After getting Acid value of less than 20, preferably less than 10 the product is poured in to trays to get solid flakes/briquettes. Both the steps also can be carried out simultaneously.
The binder/structurant of the present invention may be used with various commercially available surfactants such as Galaxy LES 70 (sodium lauryl ether sulphate). Galaxy 100 (cocomonoethanol amide) , Galaxy 200 (lauric ethanolamide) , Galaxy LSS (lauryl sulphosuccinate) amongst others.
For evaluation of the superior characteristics of toilet preparations comprising the binder/structurant of the present
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invention surfactant blends are prepared using the above mentioned surfactants and the new binder/structurant.
The surfactant blends are prepared using homogeniser and extruded in noodle form. The homogenisation is carried out in a sigma mixer. If required the blend is heated while mixing the same in sigma mixer. This is followed with further homogenisation on triple roll mill and thereafter the mass is extruded into rods of suitable sizes at ambient temperatures. The extruded rods are then cut into desired length and stamped on stamping machine.
The invention will now be further illustrated by the following, non-limiting examples.
Examples
Examples 1 to 7 demonstrate preferred schemes for preparing the binder/structurant compound of the present invention.
EXAMPLE 1: Stearic acid ester of lauric mono ethanol amide (Compound 1)
In a glass flask 1 mole of stearic acid is taken along with one mole of lauric mono ethanol amide and melted under nitrogen purging. The same is further heated to 170 to 210 degree centigrade with stirring till the acid value is brought down to less than 20. At this stage vacuum of 30 to 300 mm of Hg is applied to remove residual quantities of water. The molten mass is poured and cooled in a tray to get soft solid briquettes.
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EXAMPLE 2: Distilled palm fatty acid ester of palm fatty mono ethanol amide. (Compound 2)
In a glass flask 1.66 mole of distilled Palm fatty acid is taken along with one mole of mono ethanol amine. The mass is heated to melt under nitrogen purging. The same is further heated to 150 to 200 degree centigrade with stirring till the acid value is brought down to less than 10. The molten mass is poured and cooled in to tray to get soft solid briquettes.
EXAMPLE 3: Stearic acid ester of stearic di ethanol amide. (Compound 3)
In a glass flask 2.17 mole of stearic acid is taken along with
one mole of di ethanol amine and melted under nitrogen purging.
The same is heated further to 120 to 180 degree centigrade with
stirring till the acid value is brought down to less than 20.
The molten mass is poured and cooled in to tray to get soft
solid briquettes.
EXAMPLE 4: Stearic acid ester of stearic mono ethanol amide. (Compound 4)
In a glass flask 1.63 mole of stearic acid is taken along with
one mole of mono ethanol amine and melted under nitrogen
purging. The same is heated further to 150 to 210 degree
centigrade with stirring till the acid value is brought down to
less than 10. The molten mass is poured and cooled in to tray to
get soft solid briquettes.
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EXAMPLE 5: Lauric ester of lauric mono ethanol amide. (Compound 5)
In a glass flask 1 mole each of lauric acid and one mole of
lauric mono ethanol amide is taken and melted under nitrogen
purging. The same is heated further to 17 0 to 210 degree
centigrade with stirring still the acid value is brought down to
less than 20. The molten mass is poured and cooled in to tray to
get soft solid briquettes.
EXAMPLE 6: Stearic acid di ester of lauric di ethanol amide. (Compound 6)
Step 1: 1 mole each of lauric acid and di ethanol amine is taken in a glass flask. The same is slowly melted by heating under nitrogen purging. It is further heated under stirring to temperature 140 to 170 degree centigrade till the acid value is less than 10. The molten mass is poured and cooled in to tray to get soft solid briquettes.
Step 2: In a glass flask 1.8 mole of stearic acid is taken along with one mole of above lauric di ethanol amide is taken and melted under nitrogen purging. The same is heated further to 170 to 200 degree centigrade with stirring still the acid value is brought down to less than 40. The molten mass is poured and cooled in to tray to get soft solid briquettes.
EXAMPLE 7: Stearic acid di ester of coco di ethanol amide. (Compound 7)
In a glass flask 1.8 mole of stearic acid is taken along with
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one mole of coco di ethanol amide is taken and melted under nitrogen purging. The same is heated further to 140 to 180 degree centigrade with stirring still the acid value is brought down to less than 30. The molten mass is poured and cooled in to tray to get soft solid briquettes.
Surfactant blends A to Q comprising commercially available surfactants and the binder/structurant of the present invention is prepared. The corresponding compositions are shown in table 1.
Table 1

Blend No. Sodium
cocyl
isethionate Galaxy LSS New
efficient
binder Name of
the
binder. Steari c acid
A 60.0 0.0 30.0 Compound 1 10.0
B 60.0 0.0 40.0 Compoundl 0.0
C 56.6 10.0 0.0 - 33.3
D 56.6 10.0 0.0 - 0.0
E 56.6 10.0 33.3 Compound 1 0.0
F 56.3 18.8 25.0 Compound 2 0.0
G 56.3 18.8 25.0 Compound 3 0.0
H 75.0 25.00 0.0 - 0.0
I 56.3 18.75 25.0 Compound 4 0.0
J 56.3 18.75 0.0 - 25.0
K 56.3 18.75 25.0 Compound 5 0.0
L 56.3 18.75 25.0 Compound 1 0.0
M 56.3 18.75 25.0 Compound 6 0.0
N 56.3 18.75 25.0 Compound 7 0.0
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Blend No. Sodium
cocyl
isethionate Galaxy LSS New
efficient binder Name of the binder. Steari c acid
0 60.0 0.00 29.8 Compound 1 10.4
P 50.7 0.00 34.3 Compound 1 14.9
Blend Q:
Galaxy LES 70: 21 parts, Galaxy 789: 40.3 parts, Galaxy LSS:
38.7 parts.
Galaxy LES 70: Sodium lauryl ether sulphate, Galaxy 789: Sodium
lauryl sulphate powder, Galaxy LSS: Disodium lauryl sulphate.
In all blends titanium dioxide 0.5%, EDTA-disodium 0.1%, colour 0.8 % and perfume 25 ppm are added.
Examples 8 to 30 demonstrate bath preparations made by using blends shown in Table 1.
The evaluation of foaming and mush has been done by adopting procedure as per Bureau of Indian Standards, "Bathing Bar specification" {First revision) IS 13498:1997.
Few preparations are evaluated for eye irritation by panel of five people. This is done using 2.0 % solution of preparation in distilled water. This solution is used to wash face by the persons on the panel. Testing persons have been asked to open the eyes without rinsing off the solution for 30 seconds. Their feeling of irritation in eye is noted as irritant or non-irritant .
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Example 8
Surfactant blend-A 95 parts, demineralised water 5.0 parts are
processed to get a soap bar.
In evaluation, foam is found to be 480 ml and mush is found to
be -1.76 grams per 50 cm2 area.
Example 9
Surfactant blend-B 60 parts, strearic acid 10 parts,
demineralised water 5.0 parts and talc 25 parts are processed to
get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be -1.9 grams per 50 cm2 area.
Example 10
Surfactant blend-B 60 parts, paraffin wax 10 parts,
demineralised water 5.0 parts and talc 25 parts are processed to
get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be -0.43 grams per 50 cm2 area.
Example 11
Surfactant blend-B 70 parts, demineralised water 5.0 parts and
talc 25 parts are processed to get a soap bar.
In evaluation, foam is found to be 500 ml and mush is found to
be -4.26 grams per 50 cm2 area.
Example 12
Sodium soap using palm fatty (iodine value 35) 40 parts, demineralised water 5.0 parts and talc 55 parts are processed to get a soap bar.
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In evaluation, foam is found to be 430 ml and mush is found to be -11.26 grams per 50 cm2 area.
Example 13
Surfactant blend-C 45 parts, demineralised water 7.0 parts and
talc 48 parts are processed to get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be +1.91 grams per 50 cm2 area.
Example 14
Surfactant blend-D 45 parts, demineralised water 7.0 parts and
talc 48 parts are processed to get a soap bar.
In evaluation, foam is found to be 460 ml and mush is found to
be -7.01 grams per 50 cm2 area.
Example 15
Surfactant blend-E 45 parts, demineralised water 7.0 parts and
talc 48 parts are processed to get a soap bar.
In evaluation, foam is found to be 480 ml and mush is found to
be -9.12 grams per 50 cm2 area.
Example 16
Surfactant blend-E 45 parts, sodium soap using palm fatty acid
(iodine value 35) 5 parts, demineralised water 7.0 parts and
talc 43 parts are processed to get a soap bar.
In evaluation, foam is found to be 330 ml and mush is found to
be -5.11 grams per 50 cm2 area.
Example 17
Surfactant blend-F 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
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In evaluation, foam is found to be 400 ml and mush is found to be -10.43 grams per 50 cm2 area.
Example 18
Surfactant blend-G 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 460 ml and mush is found to
be -11.16 grams per 50 cm2 area.
Example 19
Surfactant blend-H 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 600 ml and mush is found to
be -33.97 grams per 50 cm area.
Example 20
Surfactant blend-I 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be -21.5 grams per 50 cm2 area.
Example 21
Surfactant blend-J 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be -1.86 grams per 50 cm2 area.
Example 22
Surfactant blend-K 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
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In evaluation, foam is found to be 420 ml and mush is found to be -15.47 grams per 50 cm2 area.
Example 23
Surfactant blend-L 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 4 60 ml and mush is found to
be -13.01 grams per 50 cm2 area.
Example 24
Surfactant blend-M 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 400 ml and mush is found to
be -11.26 grams per 50 cm2 area.
Example 25
Surfactant blend-N 40 parts, demineralised water 7.0 parts and
talc 53 parts are processed to get a soap bar.
In evaluation, foam is found to be 460 ml and mush is found to
be -4.67 grams per 50 cm2 area.
Example 26
Surfactant blend-0 94.4 parts and demineralised water 4.94 parts
are processed to get a soap bar.
In evaluation, foam is found to be 4 80 ml and mush is found to
be -1.76 grams per 50 cm2 area.
Example 27
Surfactant blend-P 68.6 parts, demineralised water 5.1 parts and
talc 25.6 parts are processed to get a soap bar.
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In evaluation, foam is found to be 4 00 ml and mush is found to be -1.9 grams per 50 cm2 area.
Example 28
Surfactant blend-Q 45.5 parts, stearic acid 31.8 parts, sodium
sulphate 15 parts and demineralised water 7.5 parts are
processed to get a soap bar.
In evaluation, foam is found to be 350 ml and mush is found to
be -2.69 grams per 50 cm2 area.
Example 29
Surfactant blend-Q 45.5 parts, blender compound number 1, 31.8
parts, sodium sulphate 15 parts and demineralised water 7.5
parts are processed to get a soap bar.
In evaluation, foam is found to be 560 ml and mush is found to
be -11.37 grams per 50 cm2 area.
Example 30
Market sample of well known synthetic detergent bar Dove when
evaluated shows foaming of 410 ml and mush is found to be -3.96
grams per 50 cm2 area. These values are treated as bench mark
performance.
Thus it is found from the above examples that the novel compound acts as an improved binder/structurant for usage in synthetic detergent bath preparations giving improved performance with respect to mushiness, foaming and rinsability. Such synthetic detergent bars can be prepared without usage of soap. Thus truly
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soapless toilet preparations can be prepared. Moreover, fatty acid, a major conventional binder used for making of synthetic detergent bar can be minimised or avoided. Reduction in use of hydrophobic binders also allows lower usage of actives. Due to high performance of the preparations more neutral structurants can be added. This translates in to cost efficient formulations. Reduced actives and skin pH range of the formulation give milder preparations.
Advantages of the invention:
The main advantage of the invention is, binders are provided for milder skin friendly detergent formulation, which does not depress the foam, unlike the conventional binders used in the such formulations.
The another advantage of the formulation is that since the binder does not depress the foam, one can use lower surface active content and thus make the formulation cheaper. This lower surface active substance requirement also allows one to add more non surfactant neutral fillers such as starch and talc in to the formulation making is more user friendly and economical.
Another advantage of this invention is, fatty acid soap is also not required if suggested binders are used, hence the pH is more efficiently controlled. Thus apart from making the preparation cheaper, skin friendly it can allow one to have pH of the formulation in skin pH range of 5.5 to 6.5. This also means a truly soap less preparation can be made in solid form for use as toilet bath preparation. The neutral fillers not only make the formulation cheaper, but being soap less still make it more skin friendly and milder.
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We claim:
1.A detergent composition comprising
a. A binder and structurant of formula 1,2, 3 or mixture.
b. surfactants
c. talc powder and demineralised water
herein a compound of formula 1
Rx - CO -N(H)Z -((CH2CH20 - (CH2CH20)n)x - CO - R2)y (1)
wherein, Rx and R2 are alkyl groups, and selected from 6 to 20
carbon atoms;
n = 0 to 10;
x = 1 to 10; y = 1 or 2 and Z = 0 or 1
wherein when y = 1, then z = 1 and when y = 2, then z = 0.
In which a compound of formula 1, wherein y = 1 and z = 1 such that the compound of formula 1 is a compound of formula 2.
Rl — CO - NH - CH2CH20 - ( {CH2CH20) n) x — CO — R2 (2)
wherein, Rx and R2 are alkyl groups, and selected from 6 to 20
carbon atoms;
n - 0 to 10;
x = 1 to 10;
in which a compound of formula 1, wherein y = 2 and z = 0 such that the compound of formula 1 is a compound of formula 3.
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Rl — CO — N — { (CH2CH20 — wherein, Rx and R2 are alkyl groups, and selected from 6 to 20
carbon atoms;
n = 0 to 10; x = 1 to 10;
2.A detergent composition as claimed in 1 where in surfactant are selected from sodium alkyl ether sulphate, sodium alkyl sulphate, disodium alkyl sulphosuccinate, alpha olefin sulphate, alkyl isethionate, alkyl mono ethanol amide, alkyl di ethanol amide. Alkyl group can consist of C8 to C22 carbon atoms, from 0 up to 3 double bonds, their mixture or individual carbon .
3.A detergent composition as claimed in claim 1 , wherein the filler used from 5 to 50% by , preferably from 15 to 35% by mass of the binder ,
4.A detergent composition as claimed in claim 1, wherein the said binder and structurant is present in an amount of 10% to 60% by weight of the total composition.
5.A detergent composition as claimed in claim 4, wherein the said binder and structurant is present in an amount of 10% to 40% by weight of the total composition.
6.A detergent composition as claimed in claim 1, wherein the compound of formula 1 is stearic acid ester of lauric mono ethanol amide.
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7.A detergent composition as claimed in claim 1, wherein the
compound of formula 1 is palm fatty acid ester of palm
fatty mono ethanol amide. 8 .A detergent composition as claimed in claim 1, wherein the
compound of formula 1 is stearic acid ester of stearic di
ethanol amide. 9.A detergent composition as claimed in claim 1, wherein the
compound of formula 1 is stearic acid ester of stearic mono
ethanol amide. 10.A detergent composition as claimed in claim 1, wherein
the compound of formula 1 is lauric ester of lauric mono
ethanol amide. 11.A detergent composition as claimed in claim 1, wherein the
compound of formula 1 is stearic acid di ester of lauric di
ethanol amide. 12.A detergent composition as claimed in claim 1, wherein
the compound of formula 1 is stearic acid di ester of coco
di ethanol amide.
is 18"' day of November, 2002

For Ga
urfactants Limited
Drl Kerninath P.Pandit
Sr. Manager (Application Development)
(One of the inventor)
Registered Office Address: Galaxy
Surfactants Limited
C/49-2, TTC Indl. Area, Pawne, Navi
Mumbai - 4 00 703,Maharashtra, India

(Applicant

... page 23

Documents:

1007-mum-2002-abstract(19-04-2004).doc

1007-mum-2002-abstract(19-04-2004).pdf

1007-mum-2002-cancelled pages(19-04-2004).pdf

1007-mum-2002-claims(granted)-(19-04-2004).doc

1007-mum-2002-claims(granted)-(19-04-2004).pdf

1007-mum-2002-correspondence(19-04-2004).pdf

1007-mum-2002-correspondence-(ipo)-(13-01-2005).pdf

1007-mum-2002-form 1(20-11-2002).pdf

1007-mum-2002-form 19(24-06-2003).pdf

1007-mum-2002-form 2(granted)-(19-04-2004).doc

1007-mum-2002-form 2(granted)-(19-04-2004).pdf

1007-mum-2002-form 3(19-04-2004).pdf


Patent Number 205084
Indian Patent Application Number 1007/MUM/2002
PG Journal Number 30/2008
Publication Date 25-Jul-2008
Grant Date 14-Mar-2007
Date of Filing 20-Nov-2002
Name of Patentee GALAXY SURFACTANTS LIMITED.
Applicant Address W-44 (C), TARAPUR M.I.D.C., BOISAR,
Inventors:
# Inventor's Name Inventor's Address
1 PATIL SUDHIR GALAXY SURFACTANTS LIMITED, W-44 (C), TARAPUR M.I.D.C., BOISAR - 401506,
2 KHOJA RAHIM GALAXY SURFACTANTS LIMITED, W-44 (C), TARAPUR M.I.D.C., BOISAR-401506,
3 PANDIT KASHINATH GALAXY SURFACTANTS LIMITED, W-44 (C), TARAPUR M.I.D.C., BOISAR-401506
4 MEHER BIPIN GALAXY SURFACTANTS LIMITED, W-44 (C), TARAPUR M.I.D.C., BOISAR-401506,
PCT International Classification Number C 11 D 3/00
PCT International Application Number N/A
PCT International Filing date
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 NA