RU2000107793A - CATIONIC SUGAR-CONTAINING SURFACE-ACTIVE SUBSTANCES OBTAINED FROM ETHOXYLED AMMONIUM COMPOUNDS AND REDUCING SUGARIDS - Google Patents
CATIONIC SUGAR-CONTAINING SURFACE-ACTIVE SUBSTANCES OBTAINED FROM ETHOXYLED AMMONIUM COMPOUNDS AND REDUCING SUGARIDSInfo
- Publication number
- RU2000107793A RU2000107793A RU2000107793/04A RU2000107793A RU2000107793A RU 2000107793 A RU2000107793 A RU 2000107793A RU 2000107793/04 A RU2000107793/04 A RU 2000107793/04A RU 2000107793 A RU2000107793 A RU 2000107793A RU 2000107793 A RU2000107793 A RU 2000107793A
- Authority
- RU
- Russia
- Prior art keywords
- group
- carbon atoms
- cationic sugar
- containing surfactant
- formula
- Prior art date
Links
- 150000003868 ammonium compounds Chemical class 0.000 title 1
- 239000000126 substance Substances 0.000 title 1
- 239000004094 surface-active agent Substances 0.000 claims 16
- 125000004432 carbon atoms Chemical group C* 0.000 claims 14
- 125000002091 cationic group Chemical group 0.000 claims 13
- 125000001931 aliphatic group Chemical group 0.000 claims 7
- -1 polyethyleneoxy chain Polymers 0.000 claims 6
- 150000001720 carbohydrates Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 2
- 239000012141 concentrate Substances 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 239000003752 hydrotrope Substances 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000005529 alkyleneoxy group Chemical group 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 239000008139 complexing agent Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
Claims (15)
в качестве гидротропа для поверхностно-активных веществ.1. The use of a cationic sugar-containing surfactant containing at least one hydrocarbon group with 6-24 carbon atoms and at least one quaternary ammonium group, in which at least one substituent is an alkylene-containing group, which is linked to the saccharide residue by a glycosidic bond,
as a hydrotrope for surfactants.
где R - алифатическая группа с 6-24 атомами углерода; R1 - алифатическая группа с 1-4 атомами углерода или (AO)s(G)p; R2, R3 и R4 независимо представляют собой группу (AO)s(G)p, алифатическую группу с 1-24 атомами углерода или гидроксиалкильную группу с 2-4 атомами углерода; АО - алкиленоксигруппа с 2-4 атомами углерода; s равно 0-12 и ∑s = 1-25; G, представляет собой сахаридный остаток, связанный с остатком молекулы гликозидной связью, а р (степень полимеризации) равно 0-10; ∑p = 1-20; r= 0-3; у= 2-3; Х= СО или СОО (АО)t (CqH2q) или О (АО)t(CqH2q); n= 0 или 1; n1= 0, кроме случаев, когда Х есть СО, тогда n1= l; q= 2-4; t= 0-2; u= 0 или 1, a v= 0 или 1, при условии, что сумма (v+Σu) равна 1-3, Z - анион, a z - величина заряда аниона Z.3. The use according to claim 1 or 2 of a cationic sugar-containing surfactant having the formula
where R is an aliphatic group with 6-24 carbon atoms; R 1 is an aliphatic group with 1-4 carbon atoms or (AO) s (G) p ; R 2 , R 3 and R 4 independently represent a group (AO) s (G) p , an aliphatic group with 1-24 carbon atoms or a hydroxyalkyl group with 2-4 carbon atoms; AO - alkyleneoxy group with 2-4 carbon atoms; s is 0-12 and ∑s = 1-25; G represents a saccharide residue bound to the remainder of the molecule by a glycosidic bond, and p (degree of polymerization) is 0-10; ∑p = 1-20; r is 0-3; y = 2-3; X = CO or COO (AO) t (C q H 2q ) or O (AO) t (C q H 2q ); n is 0 or 1; n 1 = 0, except when X is CO, then n 1 = l; q is 2-4; t is 0-2; u = 0 or 1, av = 0 or 1, provided that the sum (v + Σu) is 1-3, Z is the anion, az is the charge of the anion Z.
где R6 - независимо алифатическая группа с 1-4 атомами углерода или -СН2СН2OН; R7, R8 и R9 независимо друг от друга представляют собой группу (AO)s, алифатическую группу с 1-24 атомами углерода или гидроксиалкильную группу с 2-4 атомами углерода; 1= 0 или 1 и k= 0 или 1; при условии, что сумма (k+Σ1) = 1-3, a R, АО, s, X, n, n1, у и r имеют те же значения, что и в п. 3, при весовом соотношении 1: 3 - 9: 1.4. The use of claim 3, wherein the cationic sugar-containing surfactant is mixed with a quaternary ammonium compound of the formula
where R 6 is independently an aliphatic group with 1-4 carbon atoms or —CH 2 CH 2 OH; R 7 , R 8 and R 9 independently from each other represent a group (AO) s , an aliphatic group with 1-24 carbon atoms or a hydroxyalkyl group with 2-4 carbon atoms; 1 = 0 or 1 and k = 0 or 1; provided that the sum (k + Σ1) = 1-3, a R, AO, s, X, n, n 1 , y and r have the same values as in paragraph 3, with a weight ratio of 1: 3 - 9: 1.
где R - алифатическая группа с 6-24 атомами углерода, R1 - алифатическая группа с 1-4 атомами углерода или группа C2H40(G)p; G - сахаридный остаток, который связан с полиэтиленокси-цепочкой гликозидной связью, а р (степень полимеризации) равна 0-10; ∑p = 1-15, ЕО представляет собой этиленоксигруппу; s= 0-12; ∑s = 2-15; Z и z имеют значения, указанные в формуле I в пункте 3.5. The use according to claim 3, wherein the cationic sugar-containing surfactant has the formula
where R is an aliphatic group with 6-24 carbon atoms, R 1 is an aliphatic group with 1-4 carbon atoms or a group C 2 H 4 0 (G) p ; G is a saccharide residue that is linked to the polyethyleneoxy chain by a glycosidic bond, and p (degree of polymerization) is 0-10; ∑p = 1-15, EO represents an ethyleneoxy group; s is 0-12; ∑s = 2-15; Z and z have the meanings indicated in formula I in paragraph 3.
где R, R1, EO, Z- и s имеют те же значения, что и в формуле III в пункте 5, за исключением того, что р в группе R1 равно 0, при весовом соотношении 1: 3-9: 1.6. The use according to claim 5, wherein the cationic sugar-containing surfactant is mixed with a quaternary ammonium compound of the formula
where R, R 1 , EO, Z - and s have the same meanings as in formula III in paragraph 5, except that p in the group R 1 is 0, with a weight ratio of 1: 3-9: 1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9703089A SE511873C2 (en) | 1997-08-27 | 1997-08-27 | Cationic sugar surfactants from ethoxylated ammonium compounds and reducing saccharides and their use as surfactants for surfactants |
SE9703089-4 | 1997-08-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000107793A true RU2000107793A (en) | 2002-01-10 |
RU2217486C2 RU2217486C2 (en) | 2003-11-27 |
Family
ID=20408054
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000107793/04A RU2217486C2 (en) | 1997-08-27 | 1998-08-03 | Cationic sugar-containing surface-active substances prepared from ethoxylated ammonium compounds and reducing saccharides |
Country Status (15)
Country | Link |
---|---|
US (2) | US6432907B1 (en) |
EP (1) | EP1015536B1 (en) |
JP (1) | JP4067272B2 (en) |
AT (1) | ATE258218T1 (en) |
AU (1) | AU736353B2 (en) |
BR (1) | BR9811373A (en) |
CA (1) | CA2296574A1 (en) |
DE (1) | DE69821249T2 (en) |
ES (1) | ES2215311T3 (en) |
IS (1) | IS5365A (en) |
NO (1) | NO20000950L (en) |
PL (1) | PL190291B1 (en) |
RU (1) | RU2217486C2 (en) |
SE (1) | SE511873C2 (en) |
WO (1) | WO1999010462A1 (en) |
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SE514862C2 (en) | 1999-02-24 | 2001-05-07 | Akzo Nobel Nv | Use of a quaternary ammonium glycoside surfactant as an effect enhancing chemical for fertilizers or pesticides and compositions containing pesticides or fertilizers |
US20080233065A1 (en) * | 2001-06-21 | 2008-09-25 | Wang Tian X | Stable Cosmetic Emulsion With Polyamide Gelling Agent |
US8333956B2 (en) | 2002-06-11 | 2012-12-18 | Color Access, Inc. | Stable cosmetic emulsion with polyamide gelling agent |
US8449870B2 (en) * | 2002-06-11 | 2013-05-28 | Color Access, Inc. | Stable cosmetic emulsion with polyamide gelling agent |
US20050019286A1 (en) * | 2003-06-09 | 2005-01-27 | Wang Tian Xian | Stable cosmetic emulsion with polyamide |
KR20060029145A (en) * | 2003-06-26 | 2006-04-04 | 시바 스페셜티 케미칼스 홀딩 인크. | Aqueous liquid compositions of cyclodextrine or cyclodextrine derivatives and a process using the said composition |
US9055934B2 (en) * | 2004-08-26 | 2015-06-16 | Zimmer Spine, Inc. | Methods and apparatus for access to and/or treatment of the spine |
US7087560B2 (en) * | 2004-10-25 | 2006-08-08 | Unilever Home & Personal Care Usa, A Division Of Conopco, Inc. | Personal care composition with salts of dihydroxypropyltri(C1-C3 alkyl) ammonium monosubstituted polyols |
ATE515290T1 (en) * | 2004-10-25 | 2011-07-15 | Unilever Nv | PERSONAL CARE COMPOSITIONS WITH GLYCERIN AND HYDROXYPROPYL QUARTERNARY AMMONIUM SALTS |
US7659233B2 (en) * | 2004-10-25 | 2010-02-09 | Conopco, Inc. | Personal care compositions with silicones and dihydroxypropyl trialkyl ammonium salts |
US7282471B2 (en) * | 2005-09-08 | 2007-10-16 | Conopco, Inc. | Personal care compositions with glycerin and hydroxypropyl quaternary ammonium salts |
EP1951840B1 (en) * | 2005-11-14 | 2013-08-28 | Stepan Company | Viscoelastic cationic carbohydrate ether compositions |
US7659234B2 (en) * | 2006-03-07 | 2010-02-09 | Conopco, Inc. | Personal care compositions containing quaternary ammonium trihydroxy substituted dipropyl ether |
US7794741B2 (en) * | 2007-05-30 | 2010-09-14 | Conopco, Inc. | Enhanced delivery of certain fragrance components from personal care compositions |
US20080299054A1 (en) * | 2007-05-30 | 2008-12-04 | Conopco, Inc., D/B/A Unilever | Personal care compositions with enhanced fragrance delivery |
UA109772C2 (en) * | 2009-07-02 | 2015-10-12 | AGENT FOR IMPROVING SOIL HYDROPHILITY AND APPLICATION METHODS | |
US8381965B2 (en) * | 2010-07-22 | 2013-02-26 | Taiwan Semiconductor Manufacturing Company, Ltd. | Thermal compress bonding |
US8104666B1 (en) | 2010-09-01 | 2012-01-31 | Taiwan Semiconductor Manufacturing Company, Ltd. | Thermal compressive bonding with separate die-attach and reflow processes |
US8933055B2 (en) | 2010-09-22 | 2015-01-13 | Ecolab Usa Inc. | Antimicrobial compositions containing cationic active ingredients and quaternary sugar derived surfactants |
US20150272124A1 (en) | 2014-03-25 | 2015-10-01 | Ecolab Usa Inc. | Antimicrobial compositions containing cationic active ingredients |
US9956153B2 (en) | 2014-08-01 | 2018-05-01 | Ecolab Usa Inc. | Antimicrobial foaming compositions containing cationic active ingredients |
US10676694B2 (en) | 2016-12-22 | 2020-06-09 | The Procter & Gamble Company | Fabric softener composition having improved detergent scavenger compatibility |
US11261113B2 (en) | 2017-08-30 | 2022-03-01 | Ecolab Usa Inc. | Molecules having one hydrophobic group and two identical hydrophilic ionic groups and compositions thereof and methods of preparation thereof |
CN116082183A (en) | 2018-08-29 | 2023-05-09 | 埃科莱布美国股份有限公司 | Multi-charged ionic compounds derived from polyamines, compositions thereof and use thereof as reverse demulsifiers for oil and gas operations |
WO2020047015A1 (en) | 2018-08-29 | 2020-03-05 | Ecolab Usa Inc. | Use of multiple charged cationic compounds derived from primary amines or polyamines for microbial fouling control in a water system |
US11292734B2 (en) | 2018-08-29 | 2022-04-05 | Ecolab Usa Inc. | Use of multiple charged ionic compounds derived from poly amines for waste water clarification |
US11084974B2 (en) | 2018-08-29 | 2021-08-10 | Championx Usa Inc. | Use of multiple charged cationic compounds derived from polyamines for clay stabilization in oil and gas operations |
CN116396183A (en) | 2018-08-29 | 2023-07-07 | 埃科莱布美国股份有限公司 | Ionic compounds derived from polyamines, compositions thereof and methods of making the same |
EP3897143A1 (en) | 2019-01-29 | 2021-10-27 | Ecolab USA Inc. | Use of cationic sugar-based compounds for microbial fouling control in a water system |
WO2020159955A1 (en) | 2019-01-29 | 2020-08-06 | Ecolab Usa Inc. | Use of cationic sugar-based compounds as corrosion inhibitors in a water system |
WO2020214196A1 (en) | 2019-04-16 | 2020-10-22 | Ecolab Usa Inc. | Use of multiple charged cationic compounds derived from polyamines and compositions thereof for corrosion inhibition in a water system |
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WO1990015809A1 (en) * | 1989-06-16 | 1990-12-27 | Henkel Kommanditgesellschaft Auf Aktien (Henkel Kgaa) | Cationic substituted glycosides |
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-
1997
- 1997-08-27 SE SE9703089A patent/SE511873C2/en not_active IP Right Cessation
-
1998
- 1998-08-03 WO PCT/SE1998/001433 patent/WO1999010462A1/en active IP Right Grant
- 1998-08-03 CA CA002296574A patent/CA2296574A1/en not_active Abandoned
- 1998-08-03 JP JP2000507771A patent/JP4067272B2/en not_active Expired - Fee Related
- 1998-08-03 RU RU2000107793/04A patent/RU2217486C2/en not_active IP Right Cessation
- 1998-08-03 AT AT98935463T patent/ATE258218T1/en not_active IP Right Cessation
- 1998-08-03 PL PL98338993A patent/PL190291B1/en unknown
- 1998-08-03 ES ES98935463T patent/ES2215311T3/en not_active Expired - Lifetime
- 1998-08-03 EP EP98935463A patent/EP1015536B1/en not_active Expired - Lifetime
- 1998-08-03 AU AU84707/98A patent/AU736353B2/en not_active Ceased
- 1998-08-03 BR BR9811373-9A patent/BR9811373A/en not_active IP Right Cessation
- 1998-08-03 DE DE69821249T patent/DE69821249T2/en not_active Expired - Lifetime
-
2000
- 2000-01-28 IS IS5365A patent/IS5365A/en unknown
- 2000-02-25 US US09/512,856 patent/US6432907B1/en not_active Expired - Lifetime
- 2000-02-25 NO NO20000950A patent/NO20000950L/en not_active Application Discontinuation
-
2002
- 2002-06-20 US US10/177,788 patent/US6503880B1/en not_active Expired - Fee Related
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