WO2008103141A1 - Shea butter dimethyl amidopropyl amines - Google Patents
Shea butter dimethyl amidopropyl amines Download PDFInfo
- Publication number
- WO2008103141A1 WO2008103141A1 PCT/US2007/004587 US2007004587W WO2008103141A1 WO 2008103141 A1 WO2008103141 A1 WO 2008103141A1 US 2007004587 W US2007004587 W US 2007004587W WO 2008103141 A1 WO2008103141 A1 WO 2008103141A1
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- WIPO (PCT)
- Prior art keywords
- shea butter
- mild
- dmapa
- present
- processed
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/36—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/35—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/38—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
Definitions
- the present invention relates to novel shea butter dimethyl- amidopropyl amines, prepared by the reaction of dimethyl amidopropyl amine (DMAPA) and shea butter, preferably mild-processed shea butter (MPSB). These compounds are useful as cosmetic and personal care ingredients, allowing for the delivery of highly desirable active ingredients present in shea butter, including natural antioxidants, in a cationic material that is substantive to the skin and hair.
- DMAPA dimethyl amidopropyl amine
- MPSB mild-processed shea butter
- Amidoamines are well-known raw materials used as conditioning agents in the cosmetic and personal care products and conform to the following structure:
- Shea butter is a butter extracted from the kernel of Butrospermum parkii. This plant, also referred to as Vitellaria paradoxa, is native to Africa.
- the term butter describes a material that is a solid at room temperature, but melts at about 40 0 C. Chemically, shea butter is a triglyceride conforming to the following structure: 11'-C(O)-O-CH 2
- Ci 7 H 35 Stearyl 25.0 - 50.0 35.0
- R 2 The average composition of R 2 is different than R 1 and R 3 , the latter two being similar.
- the R moiety contains predominantly the unsaturated Ci 8 group (oleyl) while R and R contain predominantly the saturated Cjs group (stearyl). Differences between internal (R 2 ) and terminal (R 1 , R 3 ) substitution are seen in natural products but not in synthetic molecules produced in the laboratory.
- the novel shea butter DMAPA compounds of the present invention are produced by reacting shea butter, preferably MPSB 5 with DMAPA, preferably under specific mild processing conditions.
- mild processing is meant processes that do not remove or otherwise diminish the amount or potency of active ingredients, particularly highly desired unsaponifiables, from the mild-processed shea butter.
- mild processing is employed both at the time of harvesting and initial extraction and during subsequent preparation of derivatives. These mild processes result in materials containing unexpectedly high amounts unsaponifiables, notably antioxidants.
- U.S. Patent 5,741,915 discloses betaine compounds based on meadowfoam, including the use of meadowfoam amidopropyl dialkyl amine intermediate in the preparation of meadowfoam-based betaines. While providing conditioning properties, the materials described in the '915 Patent do not possess the desirable unsaponif ⁇ able fractions, and with them antioxidant properties, of the compounds of the present invention.
- shea butter DMAPA derivatives of the present invention thus deliver unexpectedly high amounts of unsaponifiables containing antioxidants to the skin and hair in a heretofore unachievable manner.
- the compounds of the present invention are shea butter dimethyl amidopropyl amines produced by reacting shea butter with dimethyl amidopropyl amine under mild conditions. Tn a preferred aspect of the present invention, mild processing is employed both at the time of harvesting and initial extraction (creating mild-processed shea butter) and during subsequent preparation of DMAPA derivatives.
- the novel DMAPA compounds of the present invention are rich in unsaponifiables, including antioxidants.
- the compounds of the present invention are novel amidoamines, specifically dimethyl aminopropyl amines (DMAPA), produced by reacting -shea butter with DMAPA.
- DMAPA dimethyl aminopropyl amines
- the shea butter is mild-processed and is reacted with DMAPA under mild processing conditions.
- the novel DMAPA compounds of the present invention are rich in unsaponifiables, including antioxidants and free-radical scavengers.
- Shea butter dimethyl amidopropyl amine derivatives of the present invention conform to the following structure:
- R is derived from shea butter and comprises from about 0.1 to about 2.0 % by weight Ci iH2 3 ; from about 0.5 to about 2.0% by weight Ci 3 H 27 ; from about 2.0 to about 6.0% by weight Ci 5 H 3 I ; from about 25 to about 50% by weight Ci 7 H 3S ; and from about 40.0 to about 60.0 % by weight Ci 7 H 33 .
- Another aspect of the present invention is a process for delivering antioxidants to the skin or hair by topically applying a finished product comprising an effective amount of the above-described shea butter DMAPA derivative.
- the effective concentration ranges from about 0.1 % to about 15.0% by weight of the total finished product.
- Shea butter can be prepared by standard extraction techniques known to those of skill in the art.
- U.S. Patent No. 6,552,208 the disclosure of which is incorporated herein by reference, describes several methods for processing shea butter.
- Suitable extraction vehicles may include, but are not limited to, ethanol, methanol, ethyl acetate, acetone, chloroform and water, or any other solvent and water.
- shea butter is mild-processed; it is extracted using a hydrocarbon-free solvent system and its DMAPA derivatives are made under mild processing conditions. At the time of harvesting and initial extraction ground- up kernels are boiled in water under mild conditions as described in the examples below. The oil phase is then separated from the water phase by decanting. This process yields a yellow, solid wax rich in unsaponifiables.
- wax is meant a material obtained by boiling in water under ambient conditions, decanted and filtered.
- the mild processing conditions of the present invention may be contrasted with separation using solvents and high temperature treatment with high pressure steam. While the latter processes result in what some may describe as a "more pure" triglyceride, unsaponifiables, and the benefits derived therefrom, are lost. Vacuum distillation which strips off the desirable components is also to be avoided in processing MPSB of the present invention.
- materials comprising from about 5% to about 15% by weight of unsaponifiables can be produced.
- Sterols comprise about 20% of the unsaponifiables in shea butter.
- the sterols comprise: cholesterol (from about 1% to about 3%); alpha- spinasterol (from about 1% to about 4%); delta-7-stigmasterol (from about 40% to about 44%); delta-7-avenasterol (from about 38% to about 41%).
- the remaining constituents of the unsaponifiables (about 80%) include other highly desirable active compounds including tocopherol, karitin, cinamic acid esters, alpha and beta amyrin and phenolics.
- Phenolic compounds are natural products composed of one or more aromatic benzene rings with one or more hydroxy 1 group. They are a class of natural products that possess antioxidant and free radical scavenging properties.
- phenolics in the unsaponifiables of mild-processed shea butter include gallic acid, gallocatchin, catechin, epigallocatechin gallate, epicatechin, gallocatechin gallate, gallocatechin gallate and quercetin.
- Dimethyl amidopropyl amine is an item of commerce with a molecular formula of CsHi 4 N 2 and the following structural formula:
- Another aspect of the present invention is a -shea butter DMAPA made by the amidation reaction of dimethyl aminopropyl amine and shea butter, preferably mild- processed.
- the amidation is conducted at a temperature of from about 18O 0 C to about 190 0 C.
- the starting MPSB is made according to following procedure: 500.0 grams of the nut form the shea butter tree are cracked into small pieces and placed into a one-liter vat of water. The water is then heated to 100 0 C. As the temperature increases, an oil phase develops on the surface of the water. The temperature is held for about 2 hours, after which the oil is decanted and passed through filter paper.
- the resulting butter is mild-processed shea butter according to the present invention. It is rich in unsaponifiable (from about 7% to about 15% by weight) and may be used in making the mild-processed shea butter DMAPA derivatives of the present invention.
- the mild-processed shea butter DMAPA derivatives of the present invention can be added to shampoos and body wash formulations in which the pH is then adjusted to neutral with acid including, but not limited, to hydrochloric acid, citric acid, glycolic acid, phosphoric acid, and salicylic acid.
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- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
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- Epidemiology (AREA)
- Wood Science & Technology (AREA)
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Abstract
Novel dimethyl amidopropyl amines prepared by the reaction of dimethyl amidopropyl amine (DMAPA) and shea butter, preferably mild-processed shea butter (MPSB). Materials of the present invention are useful as cosmetic and personal care ingredients, allowing for the delivery of highly desirable active ingredients present in shea butter including natural antioxidants, in a cationic material that is substantive to the skin and hair.
Description
Shea Butter Dimethyl Amidopropyl Amines Cross-Reference to Related Applications [0001] Not applicable. Statement Regarding Federally-Sponsored Research or Development
[0002] Not applicable. Field of the Invention
[0003] The present invention relates to novel shea butter dimethyl- amidopropyl amines, prepared by the reaction of dimethyl amidopropyl amine (DMAPA) and shea butter, preferably mild-processed shea butter (MPSB). These compounds are useful as cosmetic and personal care ingredients, allowing for the delivery of highly desirable active ingredients present in shea butter, including natural antioxidants, in a cationic material that is substantive to the skin and hair. Background of the Invention
[0004] Amidoamines are well-known raw materials used as conditioning agents in the cosmetic and personal care products and conform to the following structure:
CH3
I
R-C(O)-N(H)-(CH2)3-+N— H
I
CH3
At the extremes of the pH range, amidoamines are non-protonated. [0005] Shea butter is a butter extracted from the kernel of Butrospermum parkii. This plant, also referred to as Vitellaria paradoxa, is native to Africa. The term butter describes a material that is a solid at room temperature, but melts at about 400C. Chemically, shea butter is a triglyceride conforming to the following structure:
11'-C(O)-O-CH2
HC-O-C(O)-R2 R3-C(O)-O-CH2 wherein R1, R2 and R3 each have one of the following compositions:
R Group Common Name Range (%) Typical (%)
CnH23 Lauryl 0.1 - 2.0 0.2
C13H27 Myristyl 0.5 - 2.0 1.0
C15H3] Cetyl 2.0 - 6.0 4.0
Ci7H35 Stearyl 25.0 - 50.0 35.0
CnH33 Oleyl 40.0 - 60.0 59.0
Ci7H3J Linoleyl 0.5 - 1.0 0.8
[0006] The average composition of R2 is different than R1 and R3, the latter two being similar. The R moiety contains predominantly the unsaturated Ci8 group (oleyl) while R and R contain predominantly the saturated Cjs group (stearyl). Differences between internal (R2) and terminal (R1, R3) substitution are seen in natural products but not in synthetic molecules produced in the laboratory.
[0007] The high levels of stearyl and oleyl groups make shea butter and its DMAPA derivatives of particular interest in the personal care industry. While other raw materials used in personal care products have these species, the compounds of the present invention have significantly high concentrations of unsaponifiables, which posses highly desired antioxidant, ultra-violet radiation protection, and free-radical scavenging properties. Mild-processed shea butter typically contains from about 5% to about 15% by weight of unsaponifiables. In contrast, other butters commonly used in personal care products have less than 2% unsaponifiables. For example, coca butter (from Theobroma cacao) averages 0.4% unsaponifiables and Illipe butter (from Shorea stenopterά) averages 1 .1%.
[0008] As described in greater detail below, the novel shea butter DMAPA compounds of the present invention are produced by reacting shea butter, preferably MPSB5 with DMAPA, preferably under specific mild processing conditions. By "mild processed" is meant processes that do not remove or otherwise diminish the amount or potency of active ingredients, particularly highly desired unsaponifiables, from the mild-processed shea butter. In one aspect of the present invention, mild processing is employed both at the time of harvesting and initial extraction and during subsequent preparation of derivatives. These mild processes result in materials containing unexpectedly high amounts unsaponifiables, notably antioxidants.
[0008] U.S. Patent 5,741,915 discloses betaine compounds based on meadowfoam, including the use of meadowfoam amidopropyl dialkyl amine intermediate in the preparation of meadowfoam-based betaines. While providing conditioning properties, the materials described in the '915 Patent do not possess the desirable unsaponifϊable fractions, and with them antioxidant properties, of the compounds of the present invention.
[0009] The shea butter DMAPA derivatives of the present invention thus deliver unexpectedly high amounts of unsaponifiables containing antioxidants to the skin and hair in a heretofore unachievable manner. Summary of the Invention
[0010] The compounds of the present invention are shea butter dimethyl amidopropyl amines produced by reacting shea butter with dimethyl amidopropyl amine under mild conditions. Tn a preferred aspect of the present invention, mild processing is employed both at the time of harvesting and initial extraction (creating mild-processed shea butter)
and during subsequent preparation of DMAPA derivatives. The novel DMAPA compounds of the present invention are rich in unsaponifiables, including antioxidants. Detailed Description of the invention
[0011] The compounds of the present invention are novel amidoamines, specifically dimethyl aminopropyl amines (DMAPA), produced by reacting -shea butter with DMAPA. Preferably the shea butter is mild-processed and is reacted with DMAPA under mild processing conditions. The novel DMAPA compounds of the present invention are rich in unsaponifiables, including antioxidants and free-radical scavengers. [0012] Shea butter dimethyl amidopropyl amine derivatives of the present invention conform to the following structure:
CH3
wherein
R is derived from shea butter and comprises from about 0.1 to about 2.0 % by weight Ci iH23; from about 0.5 to about 2.0% by weight Ci3H27; from about 2.0 to about 6.0% by weight Ci5H3I ; from about 25 to about 50% by weight Ci7H3S; and from about 40.0 to about 60.0 % by weight Ci7H33.
[0013] Another aspect of the present invention is a process for delivering antioxidants to the skin or hair by topically applying a finished product comprising an effective amount of the above-described shea butter DMAPA derivative. In a preferred embodiment, the
effective concentration ranges from about 0.1 % to about 15.0% by weight of the total finished product. [0014] Shea Butter
[0015] Shea butter can be prepared by standard extraction techniques known to those of skill in the art. For example, U.S. Patent No. 6,552,208, the disclosure of which is incorporated herein by reference, describes several methods for processing shea butter. Suitable extraction vehicles may include, but are not limited to, ethanol, methanol, ethyl acetate, acetone, chloroform and water, or any other solvent and water. [0016] In a preferred aspect of the present invention, shea butter is mild-processed; it is extracted using a hydrocarbon-free solvent system and its DMAPA derivatives are made under mild processing conditions. At the time of harvesting and initial extraction ground- up kernels are boiled in water under mild conditions as described in the examples below. The oil phase is then separated from the water phase by decanting. This process yields a yellow, solid wax rich in unsaponifiables. By wax is meant a material obtained by boiling in water under ambient conditions, decanted and filtered.
[0017] The mild processing conditions of the present invention may be contrasted with separation using solvents and high temperature treatment with high pressure steam. While the latter processes result in what some may describe as a "more pure" triglyceride, unsaponifiables, and the benefits derived therefrom, are lost. Vacuum distillation which strips off the desirable components is also to be avoided in processing MPSB of the present invention. By processing shea butter under mild conditions, materials comprising from about 5% to about 15% by weight of unsaponifiables can be produced.
[0018] Sterols comprise about 20% of the unsaponifiables in shea butter. More particularly, the sterols comprise: cholesterol (from about 1% to about 3%); alpha- spinasterol (from about 1% to about 4%); delta-7-stigmasterol (from about 40% to about 44%); delta-7-avenasterol (from about 38% to about 41%). The remaining constituents of the unsaponifiables (about 80%) include other highly desirable active compounds including tocopherol, karitin, cinamic acid esters, alpha and beta amyrin and phenolics. [0019] Phenolic compounds are natural products composed of one or more aromatic benzene rings with one or more hydroxy 1 group. They are a class of natural products that possess antioxidant and free radical scavenging properties. Among the phenolics in the unsaponifiables of mild-processed shea butter include gallic acid, gallocatchin, catechin, epigallocatechin gallate, epicatechin, gallocatechin gallate, gallocatechin gallate and quercetin.
[0020] Dimethyl amidopropyl amine
[0021] Dimethyl amidopropyl amine is an item of commerce with a molecular formula of CsHi4N2 and the following structural formula:
CH3
I
H2N-(CHz)3-N
I
CH3
It is commercially available from a number of raw materials suppliers, including BASF (Mount Olive, NJ).
[0022] Another aspect of the present invention is a -shea butter DMAPA made by the amidation reaction of dimethyl aminopropyl amine and shea butter, preferably mild-
processed. In a preferred embodiment, the amidation is conducted at a temperature of from about 18O0C to about 1900C.
[0023J The following examples are further illustrative of the present invention. The components and specific ingredients are presented as being typical, and various modifications can be derived in view of the foregoing disclosure within the scope of the invention. All percentages, ratios and proportions herein are by weight, unless otherwise specified. All temperatures are in degrees Celsius unless otherwise specified. [0024] Examples
[0025] The starting MPSB is made according to following procedure: 500.0 grams of the nut form the shea butter tree are cracked into small pieces and placed into a one-liter vat of water. The water is then heated to 1000C. As the temperature increases, an oil phase develops on the surface of the water. The temperature is held for about 2 hours, after which the oil is decanted and passed through filter paper. The resulting butter is mild-processed shea butter according to the present invention. It is rich in unsaponifiable (from about 7% to about 15% by weight) and may be used in making the mild-processed shea butter DMAPA derivatives of the present invention.
[0026] To 455.0 grams of DMAPA is added 1450.0 grams of MPSB. Using a reflux condenser, the temperature of the mass is raised to 180° C — 1900C. The mass is held within this temperature range for 8 - 10 hours. The amine value drops during this period and, after several hours, stabilizes. Once the amine value stabilizes, the reaction mass is held an additional hour and is cooled to ambient temperature. Essential to the preparation of mild-processed shea butter DMAPA compounds of the present invention is
the low processing temperatures. This requires neither distillation of water or processing at high temperatures (e.g., from about 1800C to about 19O0C).
[0027] The mild-processed shea butter DMAPA derivatives of the present invention can be added to shampoos and body wash formulations in which the pH is then adjusted to neutral with acid including, but not limited, to hydrochloric acid, citric acid, glycolic acid, phosphoric acid, and salicylic acid.
[0028] While the illustrative embodiments of the invention have been described with particularity, it will be understood that various other modifications will be apparent to and can be readily made by those skilled in the art without departing from the spirit and scope of the invention. Accordingly, it is not intended that the scope of the claims appended hereto be limited to the examples and descriptions set forth hereinabove but rather that the claims be construed as encompassing all the features of patentable novelty which reside in the present invention, including all features which would be treated as equivalents thereof by those skilled in the art to which the invention pertains.
Claims
1. A shea butter dimethyl aminopropyl amine conforming to the structure:
CH3
I
R-C(O)-N(H)-(CH2)3-N
I
CH3 wherein
R is derived from shea butter and comprises from about 0.1 to about 2.0 % by weight CnH23; from about 0.5 to about 2.0% by weight Ci3H27; from about 2.0 to about 6.0% by weight CisH3i; from about 25 to about 50% by weight Cj7H3S; and from about 40.0 to about 60.0 % by weight Ci7H33.
2. A DMAPA derivative of claim 1 made by the amidation reaction of dimethyl amidopropyl amine and mild-processed shea butter.
3. A DMAPA derivative of claim 2 wherein the amidation is conducted at a temperature of from about 1800C to about 1900C.
4. A process for treating hair and skin with an effective concentration of a dimethyl amidopropyl amine made by the amidation reaction of dimethyl amidopropyl amine and shea butter.
5. A process for treating hair and skin of claim 4 wherein the amidation is conducted at a temperature of from about 1800C to about 1900C.
6. A shea butter dimethyl aminopropyl amine of claim 1 where the shea butter is mild- processed.
7. A process of claim 4 where the shea butter is mild-processed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2007/004587 WO2008103141A1 (en) | 2007-02-23 | 2007-02-23 | Shea butter dimethyl amidopropyl amines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2007/004587 WO2008103141A1 (en) | 2007-02-23 | 2007-02-23 | Shea butter dimethyl amidopropyl amines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2008103141A1 true WO2008103141A1 (en) | 2008-08-28 |
Family
ID=39710325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2007/004587 WO2008103141A1 (en) | 2007-02-23 | 2007-02-23 | Shea butter dimethyl amidopropyl amines |
Country Status (1)
| Country | Link |
|---|---|
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5741915A (en) * | 1995-08-17 | 1998-04-21 | Fan Tech Ltd. | Meadowfoam betaines |
| US20060128596A1 (en) * | 2004-12-13 | 2006-06-15 | Koshti Nirmal M | Aqueous composition of a betaine with solids content of at least 45% by weight |
| US7163916B2 (en) * | 2004-11-17 | 2007-01-16 | Goldschmidt Gmbh | Process for the preparation of highly concentrated flowable aqueous solutions of betaines |
-
2007
- 2007-02-23 WO PCT/US2007/004587 patent/WO2008103141A1/en active Application Filing
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5741915A (en) * | 1995-08-17 | 1998-04-21 | Fan Tech Ltd. | Meadowfoam betaines |
| US7163916B2 (en) * | 2004-11-17 | 2007-01-16 | Goldschmidt Gmbh | Process for the preparation of highly concentrated flowable aqueous solutions of betaines |
| US20060128596A1 (en) * | 2004-12-13 | 2006-06-15 | Koshti Nirmal M | Aqueous composition of a betaine with solids content of at least 45% by weight |
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