Composition comprising salt of acyl glutamate as primary surfactant or primary anionic surfactant
US-2017333320-A1 · Nov 23, 2017 · US
US10328005B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10328005-B2 |
| Application number | US-201515526855-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 12, 2015 |
| Priority date | Nov 18, 2014 |
| Publication date | Jun 25, 2019 |
| Grant date | Jun 25, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention relates to compositions comprising salt of acyl glutamate as primary surfactant or primary anionic surfactant and specific structurant polymers.
Opening claim text (preview).
The invention claimed is: 1. Cleansing composition comprising: a) 0.5 to 35% by wt. total composition of a surfactant system comprising anionic surfactant comprising salt of acyl glutamate, wherein salt of acyl glutamate is present at 50% or more of all surfactant present, and wherein the surfactant system further comprises 0 to 20% by wt. total composition of a co-surfactant, wherein co-surfactant are surfactants which are not anionic, selected from the group consisting of nonionic, cationic, amphoteric surfactants and mixtures thereof; b) 0% to 30% by wt. total composition water-soluble or oil-soluble skin or hair benefit agent not being a surfactant; c) 0.1 to 10% of a structuring polymer which is a polymerization product of: i) 0 to 10% by wt. of total monomer of a first ethylenically unsaturated monomer selected from the group consisting of: A) diacids of formula HOOC—CR 1 ═CR 2 —COOH (I); B) a cyclic anhydride precursor of diacid (I), having the formula: C) and combination thereof, where R 1 and R 2 are individually selected from H, C 1 -C 3 alkyl, phenyl, chlorine and bromine; ii) 15 to 60% by wt. total monomer of a second ethylenically unsaturated monomer selected from the group consisting of acrylic acid, methacrylic acid and mixtures thereof; iii) 30 to 75% by wt. of total monomer of a (meth)acrylate monomer which is selected from the group consisting of C 1 to C 8 esters of acrylic acid, C 1 to C 8 esters of methacrylic acid and mixtures thereof; and iv) 1 to 25% by wt. of total monomer of an associative monomer having the formula: R 4 —CH═C(R 3 )—C(O)—O—(R 5 O) a —R 6 wherein: R 3 and R 4 are independently selected from H and C 1-3 alkyl, each R 5 O is independently an oxyalkylene unit having from 2 to 4carbon atoms, R 6 is selected from: linear and branched alkyl having from 8 to 40 carbon atoms, and alkaryl, the alkyl group of which has from 8 to 40 carbon atoms, such alkyl group being linear or branched; and a has a value of from 6 to 40; and d) water and wherein salt of glutamate comprises a mixture of C 10 and C coco glutamate, wherein the mixture of C 10 and C coco has a C 8 -C 10 chain length distribution wherein C 8 -C 10 is present in an amount of more than 13%, or salt of glutamate comprises a mixture of C 10 and C 12 glutamate, wherein the ratio of C 10 to C 12 is at least 1/5, wherein pH of composition is 5.5 or below. 2. A composition according to claim 1 , wherein the composition is clear isotropic, wherein clear isotropic is defined by absorbance value of 1.0 or below when measured at wavelength of 550 nm, adding 300 μl into a 96-well plate without dilution. 3. A composition according to claim 1 , wherein salt of glutamate comprises a mixture of C 10 and C coco glutamate wherein the mixture of C 10 and C coco has a C 8 -C 10 chain length distribution wherein C 8 -C 10 is present in an amount of more than 13%. 4. A composition according to claim 1 , further comprising 0.1% to 10% by wt. benefit agent not being a surfactant. 5. A composition according to claim 1 wherein pH of composition is 4.0 to 6.0. 6. A composition according to claim 1 , wherein pH is 4 to 5.5. 7. A composition according to claim 1 , wherein co-surfactant is cocoamidopropylbetaine and which comprises 0.1 to 2% C 10 -C 14 fatty acid. 8. Composition according to claim 1 , wherein co-surfactant is CAPB and level of MgCl 2 is 0.8% to 3.0%. 9. A composition according to claim 1 , which has initial bulk viscosity at shear rate of 1.0 s −1 of greater than 1,000 cps. 10. A composition according to claim 1 , which remains clear and whose bulk viscosity at shear rate of 1.0 s −1 , measured by a stress-controlled rheometer, remains significantly stable (±30%) from when measured before and after two weeks at storage temperatures of 4° C., 25° C. and 50° C.; and which composition has no visible phase separation after storage of two weeks at temperatures of 4° C., 25° C. and 50° C. 11. A composition according to claim 1 , subparagraph (iv), wherein the alkaryl group is alkylphenyl.
Transparent; Translucent · CPC title
Preparations for cleaning the hair · CPC title
Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof · CPC title
Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof · CPC title
Thickener, Thickening system · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.