KR20190020320A - 수성 계면활성제 조성물 - Google Patents
수성 계면활성제 조성물 Download PDFInfo
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- KR20190020320A KR20190020320A KR1020197000773A KR20197000773A KR20190020320A KR 20190020320 A KR20190020320 A KR 20190020320A KR 1020197000773 A KR1020197000773 A KR 1020197000773A KR 20197000773 A KR20197000773 A KR 20197000773A KR 20190020320 A KR20190020320 A KR 20190020320A
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- 150000001875 compounds Chemical class 0.000 claims abstract description 65
- 239000000194 fatty acid Substances 0.000 claims abstract description 20
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- POPRCUFMXZJTQI-UHFFFAOYSA-N oxomethanedisulfonic acid Chemical class OS(=O)(=O)C(=O)S(O)(=O)=O POPRCUFMXZJTQI-UHFFFAOYSA-N 0.000 claims abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical class O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229920006317 cationic polymer Polymers 0.000 claims abstract description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
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- -1 salt sulfo fatty acid Chemical class 0.000 claims description 33
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 239000011734 sodium Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 229910052708 sodium Inorganic materials 0.000 claims description 19
- 229910052791 calcium Inorganic materials 0.000 claims description 17
- 229910052700 potassium Inorganic materials 0.000 claims description 17
- 229910052744 lithium Inorganic materials 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 13
- OYINQIKIQCNQOX-UHFFFAOYSA-M 2-hydroxybutyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCC(O)C[N+](C)(C)C OYINQIKIQCNQOX-UHFFFAOYSA-M 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 9
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 9
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 claims description 9
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 9
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 9
- 229920000289 Polyquaternium Polymers 0.000 claims description 8
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- 244000007835 Cyamopsis tetragonoloba Species 0.000 claims description 4
- 229920002472 Starch Polymers 0.000 claims description 4
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- GDNCXORZAMVMIW-UHFFFAOYSA-N dodecane Chemical compound [CH2]CCCCCCCCCCC GDNCXORZAMVMIW-UHFFFAOYSA-N 0.000 claims description 4
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- 229920000688 Poly[(2-ethyldimethylammonioethyl methacrylate ethyl sulfate)-co-(1-vinylpyrrolidone)] Polymers 0.000 claims description 3
- 229920006322 acrylamide copolymer Polymers 0.000 claims description 3
- 229920002553 poly(2-methacrylolyloxyethyltrimethylammonium chloride) polymer Polymers 0.000 claims description 3
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 244000037364 Cinnamomum aromaticum Species 0.000 claims 1
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 claims 1
- 230000003796 beauty Effects 0.000 claims 1
- 239000008257 shaving cream Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 abstract description 15
- 239000002537 cosmetic Substances 0.000 abstract description 8
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- 230000001953 sensory effect Effects 0.000 abstract description 3
- 238000009472 formulation Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 14
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- 238000004140 cleaning Methods 0.000 description 6
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- 230000000052 comparative effect Effects 0.000 description 4
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- 238000000034 method Methods 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 230000019635 sulfation Effects 0.000 description 4
- 238000005670 sulfation reaction Methods 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
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- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
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- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
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- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
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- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
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- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
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- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 1
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- 230000001771 impaired effect Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- PYIDGJJWBIBVIA-UYTYNIKBSA-N lauryl glucoside Chemical compound CCCCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O PYIDGJJWBIBVIA-UYTYNIKBSA-N 0.000 description 1
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- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
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- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
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Classifications
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- A61K8/23—Sulfur; Selenium; Tellurium; Compounds thereof
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
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- A61K8/41—Amines
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Landscapes
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- Life Sciences & Earth Sciences (AREA)
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- Veterinary Medicine (AREA)
- Birds (AREA)
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- Dermatology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
- Oral & Maxillofacial Surgery (AREA)
Abstract
Description
Claims (5)
- 하기를 포함하는 수성 계면활성제 조성물:
ㆍ 일반식 (I) 의 하나 이상의 알파- 술포 지방산 2염 (A):
R1CH(SO3M1)COOM2 (I)
[식 중, 라디칼 R1 은 6 내지 18 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 또는 알케닐 라디칼이고, 라디칼 M1 및 M2 는 - 서로 독립적으로 - H, Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨],
ㆍ 화합물 (F) 및 화합물 (G) 에서 선택되는 하나 이상의 술포케톤 (B) 로서,
화합물 (F) 가 일반식 (VI) 를 갖고:
R6CH2-CO-CHR7(SO3M8) (VI)
[식 중, 라디칼 R6 및 R7 은 - 서로 독립적으로 - 6 내지 18 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 라디칼이고, 라디칼 M8 은 H, Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨],
화합물 (G) 가 일반식 (VII) 을 갖는, 하나 이상의 술포케톤 (B):
(SO3M9)R8CH-CO-CHR9(SO3M10) (VII)
[식 중, 라디칼 R8 및 R9 는 - 서로 독립적으로 - 6 내지 18 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 라디칼이고, 라디칼 M9 및 M10 은 - 서로 독립적으로 - H, Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨],
ㆍ INCI 명칭 폴리쿼터늄-6, 폴리쿼터늄-7, 폴리쿼터늄-10, 폴리쿼터늄-11, 폴리쿼터늄-16, 폴리쿼터늄-22, 폴리쿼터늄-24, 폴리쿼터늄-32, 폴리쿼터늄-37, 폴리쿼터늄-39, 폴리쿼터늄-44, 폴리쿼터늄-46, 폴리쿼터늄-47, 폴리쿼터늄-53, 폴리쿼터늄-67, 폴리쿼터늄-68, 폴리쿼터늄-72, 폴리쿼터늄-74, 폴리아크릴아미도프로필트리모늄 클로라이드, 폴리메타크릴아미도프로필트리모늄 클로라이드, 아크릴아미도프로필트리모늄 클로라이드/아크릴아미드 공중합체, 구아 히드록시프로필트리모늄 클로라이드, 카시아 히드록시프로필트리모늄 클로라이드 및 전분 히드록시프로필트리모늄 클로라이드를 갖는 양이온성 중합체의 군에서 선택되는 하나 이상의 양이온성 중합체 (X),
ㆍ 일반식 (III) 의 하나 이상의 화합물 (C):
R4COOM5 (III)
[식 중, 라디칼 R4 는 7 내지 19 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 또는 알케닐 라디칼이고, 라디칼 M5 는 H, Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨. 이에 관하여, 특히 바람직한 알칸올아민은 모노에탄올아민, 디에탄올아민, 트리에탄올아민 및 모노이소프로판올아민임],
ㆍ 일반식 (IV) 의 하나 이상의 황산의 무기 염 (D):
(M6)2SO4 (IV)
[식 중, M6 은 Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨. 이에 관하여, 특히 바람직한 알칸올아민은 모노에탄올아민, 디에탄올아민, 트리에탄올아민 및 모노이소프로판올아민임],
ㆍ 물,
이때, 하기 단서를 적용함:
ㆍ 수성 계면활성제 조성물이 일반식 (V) 의 하나 이상의 에스테르 술포네이트 (E) 를 포함한다면:
R2CH(SO3M7)COOR3 (V)
[식 중, 라디칼 R2 는 6 내지 18 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 또는 알케닐 라디칼이고, 라디칼 R3 은 1 내지 20 개의 탄소 원자를 갖는 선형 또는 분지형 알킬 또는 알케닐 라디칼이고, 이때 라디칼 R3 은 논리적으로 알케닐 라디칼 또는 오직 3 개 초과 탄소 원자의 분지형일 수 있고, 라디칼 M7 은 Li, Na, K, Ca/2, Mg/2, 암모늄 및 알칸올아민을 포함하는 군에서 선택됨],
화합물 (A) 는 - 화합물 (A) 및 (E) 의 전체를 기반으로 - 50 중량% 이상의 정도 - 특히 90 중량% 이상의 정도로 존재해야만 함. - 제 1 항에 있어서, 식 (I) 에서의 라디칼 R1 이 10 내지 16 개의 탄소 원자를 갖는 포화된, 선형 알킬 라디칼이고, 이때 화합물 (A) 에 관하여, 라디칼 R1 이 데실 또는 도데실 라디칼인 화합물 (A) 의 분율이 - 화합물 (A) 의 총량을 기준으로 - 90 중량% 이상인, 수성 계면활성제 조성물.
- 제 1 항 또는 제 2 항에 있어서, 라디칼 M1 및 M2 가 H (수소) 및 Na (나트륨) 을 포함하는 군에서 선택되는 수성 계면활성제 조성물.
- 제 1 항 내지 제 3 항 중 어느 한 항에 있어서, pH 가 4 내지 6 범위의 값인 수성 계면활성제 조성물.
- 헤어 샴푸, 샤워 겔, 비누, 합성 세제 (syndet), 워싱 페이스트, 워싱 로션, 스크럽 제제, 폼 배쓰, 오일 배쓰, 샤워 배쓰, 쉐이빙 폼, 쉐이빙 로션, 쉐이빙 크림 및 치아 케어 제품 형태의 미용 제품을 위한, 제 1 항 내지 제 4 항 중 어느 한 항에 따른 수성 계면활성제 조성물의 용도.
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| EP16174313.3 | 2016-06-14 | ||
| EP16174313.3A EP3257496A1 (de) | 2016-06-14 | 2016-06-14 | Wässrige tensid-zusammensetzungen |
| PCT/EP2017/061260 WO2017215849A1 (de) | 2016-06-14 | 2017-05-11 | Wässrige tensid-zusammensetzungen |
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| US2195088A (en) * | 1938-04-30 | 1940-03-26 | Ig Farbenindustrie Ag | Sulphonated ketones |
| WO2015117840A1 (de) * | 2014-02-04 | 2015-08-13 | Basf Se | WÄßRIGE TENSID-ZUSAMMENSETZUNGEN |
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| DE3707014A1 (de) | 1987-03-05 | 1988-09-15 | Henkel Kgaa | Waessrige tensidzusammensetzungen mit alpha-sulfofettsaeure-salzen |
| DE3913385A1 (de) * | 1989-04-24 | 1990-10-31 | Henkel Kgaa | Schmelz- und formbare tensidgemische in trockenform auf basis von alpha-sulfofettsaeuremethylestersalzen, verfahren zu ihrer herstellung und ihre verwendung |
| DE4220580A1 (de) | 1992-06-24 | 1994-01-13 | Henkel Kgaa | alpha-Sulfocarbonylverbindungen |
| DE19714370A1 (de) | 1997-04-08 | 1998-10-15 | Henkel Kgaa | Wäßrige pflegende Haut- und Haarbehandlungsmittel |
| US5965508A (en) * | 1997-10-21 | 1999-10-12 | Stepan Company | Soap bar compositions comprising alpha sulfonated fatty acid alkyl esters and long chain fatty acids |
| DE19909552C1 (de) * | 1999-03-04 | 2000-07-27 | Goldwell Gmbh | Haarwaschmittel |
| US20050153853A1 (en) * | 2002-01-31 | 2005-07-14 | Stepan Company | Soap bar compositions comprising alpha sulfonated alkyl ester or sulfonated fatty acid and synthetic surfactant and processes for producing same |
| ES2589787T3 (es) * | 2005-02-04 | 2016-11-16 | Stepan Company | Composición limpiadora líquida personal |
| DE102007028423A1 (de) | 2007-06-20 | 2008-12-24 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren und Vorrichtung zur Bildung von Aggregaten biologischer Zellen |
| US20120121679A1 (en) * | 2009-07-16 | 2012-05-17 | University Of Georgia Research Foundation, Inc. | Viricidal and microbicidal compositions and uses thereof |
| US10800962B2 (en) * | 2015-05-07 | 2020-10-13 | Rhodia Operations | Formulations for enhanced oil recovery comprising sulfonates |
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| US2195088A (en) * | 1938-04-30 | 1940-03-26 | Ig Farbenindustrie Ag | Sulphonated ketones |
| WO2015117840A1 (de) * | 2014-02-04 | 2015-08-13 | Basf Se | WÄßRIGE TENSID-ZUSAMMENSETZUNGEN |
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| EP3257496A1 (de) | 2017-12-20 |
| JP2019523771A (ja) | 2019-08-29 |
| US20190254946A1 (en) | 2019-08-22 |
| EP3468524A1 (de) | 2019-04-17 |
| BR112018075745B1 (pt) | 2022-01-18 |
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