JPWO2020014659A5 - - Google Patents
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- JPWO2020014659A5 JPWO2020014659A5 JP2021500674A JP2021500674A JPWO2020014659A5 JP WO2020014659 A5 JPWO2020014659 A5 JP WO2020014659A5 JP 2021500674 A JP2021500674 A JP 2021500674A JP 2021500674 A JP2021500674 A JP 2021500674A JP WO2020014659 A5 JPWO2020014659 A5 JP WO2020014659A5
- Authority
- JP
- Japan
- Prior art keywords
- weight
- composition
- fatty acid
- composition according
- active ingredient
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000000203 mixture Substances 0.000 claims 52
- 235000014113 dietary fatty acids Nutrition 0.000 claims 14
- 229930195729 fatty acid Natural products 0.000 claims 14
- 239000000194 fatty acid Substances 0.000 claims 14
- 239000004480 active ingredient Substances 0.000 claims 13
- 150000004665 fatty acids Chemical class 0.000 claims 13
- 150000002148 esters Chemical class 0.000 claims 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 7
- 125000005456 glyceride group Chemical group 0.000 claims 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 238000009472 formulation Methods 0.000 claims 4
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims 4
- 125000005314 unsaturated fatty acid group Chemical group 0.000 claims 4
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 3
- 235000019486 Sunflower oil Nutrition 0.000 claims 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 239000007795 chemical reaction product Substances 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims 3
- 239000003921 oil Substances 0.000 claims 3
- 235000019198 oils Nutrition 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 239000002600 sunflower oil Substances 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims 2
- 229940108924 conjugated linoleic acid Drugs 0.000 claims 2
- 239000004615 ingredient Substances 0.000 claims 2
- -1 jojoba oil Substances 0.000 claims 2
- 229940119170 jojoba wax Drugs 0.000 claims 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 2
- 229940127557 pharmaceutical product Drugs 0.000 claims 2
- 238000005956 quaternization reaction Methods 0.000 claims 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical group C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- JBYXPOFIGCOSSB-GOJKSUSPSA-N 9-cis,11-trans-octadecadienoic acid Chemical compound CCCCCC\C=C\C=C/CCCCCCCC(O)=O JBYXPOFIGCOSSB-GOJKSUSPSA-N 0.000 claims 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims 1
- AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 claims 1
- 235000019482 Palm oil Nutrition 0.000 claims 1
- 235000019484 Rapeseed oil Nutrition 0.000 claims 1
- 235000019498 Walnut oil Nutrition 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 claims 1
- 229940073608 benzyl chloride Drugs 0.000 claims 1
- 239000000828 canola oil Substances 0.000 claims 1
- 235000019519 canola oil Nutrition 0.000 claims 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 claims 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 claims 1
- 229940008406 diethyl sulfate Drugs 0.000 claims 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 229960003750 ethyl chloride Drugs 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 claims 1
- 125000005908 glyceryl ester group Chemical group 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 235000020778 linoleic acid Nutrition 0.000 claims 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims 1
- 229940102396 methyl bromide Drugs 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- 239000002540 palm oil Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 238000007127 saponification reaction Methods 0.000 claims 1
- 239000003549 soybean oil Substances 0.000 claims 1
- 235000012424 soybean oil Nutrition 0.000 claims 1
- 239000008170 walnut oil Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (22)
(a)前記組成物の重量に基づいて約30重量%~約100重量%の混合物、及び
(b)所望に応じて、前記組成物の0重量%~約70重量%の溶媒、
を含み、
前記混合物が
i.前記混合物の約50重量%~約80重量%を成す1又は複数のエステルクォート、及び
ii.前記混合物の約20重量%~約50重量%を成す1又は複数のグリセリド、
を含み、
前記エステルクォートは、少なくとも50重量%の不飽和脂肪酸基を有する脂肪酸源から誘導される、
組成物。 It ’s a composition,
(A) a mixture of about 30% by weight to about 100% by weight based on the weight of the composition, and (b) 0% to about 70% by weight of the solvent, optionally.
Including
The mixture is i. One or more ester quotes forming from about 50% to about 80% by weight of the mixture, and ii. One or more glycerides, which make up about 20% to about 50% by weight of the mixture.
Including
The ester quotes are derived from a fatty acid source having at least 50% by weight unsaturated fatty acid groups.
Composition.
前記アルカノールアミンが、トリエタノールアミン(TEA)、メチルジエタノールアミン(MDEA)、エチルジエタノールアミン、ジメチルアミノ-N-(2,3-プロパンジオール)、ジエチルアミノ-N-(2,3-プロパンジオール)、メチルアミノ-N,N-ビス(2,3-プロパンジオール)、エチルアミノ-N,N-ビス(2,3-プロパンジオール)、及びこれらの混合物から成る群より選択される、
請求項1に記載の組成物。 The ester quote is a quaternization reaction product of the fatty acid source and an alkanolamine at a ratio of about 1.5 to 3 mol of acyl groups per mole of the alkanolamine.
The alkanolamines are triethanolamine (TEA), methyldiethanolamine (MDEA), ethyldiethanolamine, dimethylamino-N- (2,3-propanediol), diethylamino-N- (2,3-propanediol), and methylamino. Selected from the group consisting of -N, N-bis (2,3-propanediol), ethylamino-N, N-bis (2,3-propanediol), and mixtures thereof.
The composition according to claim 1.
(a)0.01重量%~約30重量%の組成物活性成分であって、
i.前記組成物活性成分の重量に基づいて、約50%~約80重量%の量の1又は複数のエステルクォート、及び
ii.前記組成物活性成分の重量に基づいて、約20重量%~約50重量%の量の1又は複数のグリセリド、を含む、組成物活性成分、
(b)所望に応じて、1又は複数の追加成分、及び
(c)前記製剤を100%に合わせるための希釈剤、
を含み、
前記エステルクォートは、少なくとも50重量%の不飽和脂肪酸基を有する脂肪酸源から誘導される、
製剤。 It is a pharmaceutical product
(A) 0.01% by weight to about 30% by weight of the composition active ingredient.
i. Based on the weight of the active ingredient in the composition, an amount of about 50% to about 80% by weight of one or more ester quotes, and ii. A composition active ingredient comprising an amount of one or more glycerides, in an amount of about 20% to about 50% by weight, based on the weight of the composition active ingredient.
(B) one or more additional ingredients, as desired, and (c) a diluent to make the formulation 100%.
Including
The ester quotes are derived from a fatty acid source having at least 50% by weight unsaturated fatty acid groups.
pharmaceutical formulation.
(a)約0.01重量%~約30重量%の組成物活性成分であって、前記組成物活性成分は、
i.C8~C32の炭素鎖を有する脂肪酸源由来の少なくとも1つのエステルクォート、及び
ii.所望に応じて、C8~C32の炭素鎖を有する脂肪酸源由来のグリセリド成分、を含み、
前記少なくとも1つのエステルクォートは、少なくとも50重量%の不飽和脂肪酸基を有する脂肪酸源から誘導され、
前記グリセリド成分は、少なくとも1つのモノグリセリド、若しくはジグリセリド、又はこれらの組み合わせを含む、組成物活性成分、
(b)所望に応じて、1又は複数の追加成分、及び
(c)前記製剤を100%に合わせるための希釈剤、
を含む、ヘアケア組成物。 A hair care composition
(A) About 0.01% by weight to about 30% by weight of the active ingredient of the composition, wherein the active ingredient of the composition is
i. At least one ester quote from a fatty acid source having a carbon chain of C8-C32, and ii. If desired, it contains a glyceride component derived from a fatty acid source having a carbon chain of C8 to C32.
The at least one ester quote is derived from a fatty acid source having at least 50% by weight unsaturated fatty acid groups.
The glyceride component is a composition active ingredient containing at least one monoglyceride, or diglyceride, or a combination thereof.
(B) one or more additional ingredients, as desired, and (c) a diluent to make the formulation 100%.
A hair care composition containing.
(a)10重量%~約90重量%の組成物活性成分であって、
i.前記組成物活性成分の重量に基づいて、約50重量%~約80重量%の量の1又は複数のエステルクォート、及び
ii.前記組成物活性成分の重量に基づいて、約20重量%~約50重量%の量の1又は複数のグリセリド、を含み、
前記少なくとも1つのエステルクォートは、少なくとも50重量%の不飽和脂肪酸基を有する脂肪酸源から誘導される、組成物活性成分、
(b)所望に応じて、少なくとも1つの脂肪族アルコール、及び
(c)前記製剤を100%に合わせるための、水、溶媒、又はこれらの組み合わせを含む、希釈剤、
を含む、組成物。 It ’s a composition,
(A) 10% by weight to about 90% by weight of the composition active ingredient.
i. Based on the weight of the active ingredient of the composition, one or more ester quotes in an amount of about 50% by weight to about 80% by weight, and ii. Containing about 20% by weight to about 50% by weight of one or more glycerides, based on the weight of the active ingredient of the composition.
The composition active ingredient, wherein the at least one ester quote is derived from a fatty acid source having at least 50% by weight of unsaturated fatty acid groups.
(B) At least one fatty alcohol, if desired, and (c) a diluent comprising water, a solvent, or a combination thereof to make the formulation 100%.
A composition comprising.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862697235P | 2018-07-12 | 2018-07-12 | |
US62/697,235 | 2018-07-12 | ||
US201962839081P | 2019-04-26 | 2019-04-26 | |
US62/839,081 | 2019-04-26 | ||
PCT/US2019/041684 WO2020014659A1 (en) | 2018-07-12 | 2019-07-12 | Esterquat compositions |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2021532081A JP2021532081A (en) | 2021-11-25 |
JPWO2020014659A5 true JPWO2020014659A5 (en) | 2022-06-29 |
JP7422125B2 JP7422125B2 (en) | 2024-01-25 |
Family
ID=69142805
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2021500674A Active JP7422125B2 (en) | 2018-07-12 | 2019-07-12 | Esterquat composition |
Country Status (14)
Country | Link |
---|---|
US (1) | US20210128432A1 (en) |
EP (1) | EP3820980A4 (en) |
JP (1) | JP7422125B2 (en) |
KR (1) | KR20210030431A (en) |
CN (1) | CN112752832A (en) |
AU (1) | AU2019300158A1 (en) |
BR (1) | BR112021000482A2 (en) |
CA (1) | CA3106040A1 (en) |
CL (1) | CL2021000074A1 (en) |
CO (1) | CO2021000884A2 (en) |
MX (1) | MX2021000271A (en) |
PE (1) | PE20211244A1 (en) |
SG (1) | SG11202013227UA (en) |
WO (1) | WO2020014659A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR112022021654A2 (en) * | 2020-04-30 | 2022-12-20 | Stepan Co | COMPOSITIONS OF CONCENTRATED LIQUID ESTERQUAT |
EP4019616A1 (en) * | 2020-12-24 | 2022-06-29 | Kao Corporation, S.A. | Quaternary ester ammonium compound compositions |
EP4360617A1 (en) | 2022-10-31 | 2024-05-01 | Evonik Operations GmbH | Formulation comprising ester quats based on trialkanolamines |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0636356B1 (en) * | 1993-07-27 | 2000-12-20 | Stepan Company | Hair conditioner compositions containing fatty acid ester derivatives of alkanolamines |
DE4334365A1 (en) * | 1993-10-08 | 1995-04-13 | Henkel Kgaa | Quaternized fatty acid triethanolamine ester salts with improved water solubility |
US5869716A (en) * | 1994-03-18 | 1999-02-09 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of esterquats |
DE4409322C1 (en) * | 1994-03-18 | 1995-04-06 | Henkel Kgaa | Process for the preparation of ester quats |
AU1693197A (en) * | 1996-01-05 | 1997-08-01 | Stepan Company | Articles and methods for treating fabrics based on acyloxyalkyl quaternary ammonium compositions |
US5916863A (en) * | 1996-05-03 | 1999-06-29 | Akzo Nobel Nv | High di(alkyl fatty ester) quaternary ammonium compound from triethanol amine |
WO1999035120A1 (en) * | 1998-01-09 | 1999-07-15 | Witco Corporation | Novel quaternary ammonium compounds, compositions containing them, and uses thereof |
DE19805703C2 (en) * | 1998-02-06 | 2001-05-03 | Cognis Deutschland Gmbh | Hair care products |
DE19851427A1 (en) | 1998-11-09 | 2000-05-11 | Cognis Deutschland Gmbh | Use of cationic mixtures |
DE10022966A1 (en) | 2000-05-11 | 2001-11-22 | Cognis Deutschland Gmbh | Process for the preparation of ester quats |
DE102004024509B4 (en) * | 2004-05-18 | 2006-06-08 | Henkel Kgaa | Procedures and preparations for the restructuring of hair |
GB0717485D0 (en) * | 2007-09-08 | 2007-10-17 | Unilever Plc | Improvements relating to fabric conditioners |
ES2726054T3 (en) * | 2010-10-25 | 2019-10-01 | Stepan Co | Alkoxylated fatty esters and derivatives of natural oil metathesis |
CN103201254B (en) * | 2010-10-25 | 2016-01-20 | 斯特潘公司 | From the metathetic ester amine of natural oil and derivative |
EP2648808B1 (en) * | 2010-12-10 | 2015-03-18 | Thor Especialidades S.A. | Compositions comprising quaternary ammonium compounds |
DE102010063590A1 (en) * | 2010-12-14 | 2011-09-22 | Henkel Ag & Co. Kgaa | Hair treatment agent useful e.g. for improving wet and dry combability of keratin fibers, comprises dicocoyl pentaerythrityl distearyl citrate, quaternary ammonium compound and a nourishing fat component comprising silicones or oil bodies |
EP2764860A1 (en) * | 2013-02-06 | 2014-08-13 | Basf Sa | Cupuassu fatty acid amidoamines and their derivatives |
US10894932B2 (en) * | 2016-08-18 | 2021-01-19 | The Procter & Gamble Company | Fabric care composition comprising glyceride copolymers |
-
2019
- 2019-07-12 AU AU2019300158A patent/AU2019300158A1/en active Pending
- 2019-07-12 CA CA3106040A patent/CA3106040A1/en active Pending
- 2019-07-12 KR KR1020217004010A patent/KR20210030431A/en unknown
- 2019-07-12 BR BR112021000482-3A patent/BR112021000482A2/en unknown
- 2019-07-12 JP JP2021500674A patent/JP7422125B2/en active Active
- 2019-07-12 MX MX2021000271A patent/MX2021000271A/en unknown
- 2019-07-12 EP EP19835193.4A patent/EP3820980A4/en active Pending
- 2019-07-12 PE PE2021000047A patent/PE20211244A1/en unknown
- 2019-07-12 SG SG11202013227UA patent/SG11202013227UA/en unknown
- 2019-07-12 CN CN201980046657.2A patent/CN112752832A/en active Pending
- 2019-07-12 WO PCT/US2019/041684 patent/WO2020014659A1/en unknown
-
2021
- 2021-01-11 CL CL2021000074A patent/CL2021000074A1/en unknown
- 2021-01-11 US US17/145,999 patent/US20210128432A1/en active Pending
- 2021-01-27 CO CONC2021/0000884A patent/CO2021000884A2/en unknown
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