DE19738634A1 - Niedrigviskose wäßrige Konzentrate von Alkylbetainen - Google Patents
Niedrigviskose wäßrige Konzentrate von AlkylbetainenInfo
- Publication number
- DE19738634A1 DE19738634A1 DE19738634A DE19738634A DE19738634A1 DE 19738634 A1 DE19738634 A1 DE 19738634A1 DE 19738634 A DE19738634 A DE 19738634A DE 19738634 A DE19738634 A DE 19738634A DE 19738634 A1 DE19738634 A1 DE 19738634A1
- Authority
- DE
- Germany
- Prior art keywords
- concentrates
- alkyl
- range
- content
- formula
- 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.)
- Ceased
Links
- -1 alkyl betaine Chemical compound 0.000 title claims abstract description 43
- 239000012141 concentrate Substances 0.000 title claims abstract description 38
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 title description 7
- 229960003237 betaine Drugs 0.000 title description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 22
- 229920005862 polyol Polymers 0.000 claims abstract description 17
- 150000001412 amines Chemical class 0.000 claims abstract description 16
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol Substances OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 7
- 235000000346 sugar Nutrition 0.000 claims abstract description 7
- 150000005846 sugar alcohols Chemical class 0.000 claims abstract description 7
- 150000002337 glycosamines Chemical class 0.000 claims abstract description 6
- 150000003077 polyols Chemical group 0.000 claims abstract description 6
- 238000002360 preparation method Methods 0.000 claims abstract description 6
- 238000009833 condensation Methods 0.000 claims abstract description 5
- 230000005494 condensation Effects 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000003839 salts Chemical class 0.000 claims abstract description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 3
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000007787 solid Substances 0.000 claims description 9
- 238000006482 condensation reaction Methods 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229930182478 glucoside Natural products 0.000 claims description 5
- 235000011187 glycerol Nutrition 0.000 claims description 4
- 150000008163 sugars Chemical class 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 claims description 2
- 229940120124 dichloroacetate Drugs 0.000 claims description 2
- 150000003977 halocarboxylic acids Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000000600 sorbitol Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002253 acid Substances 0.000 abstract description 2
- 229930182470 glycoside Natural products 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000009969 flowable effect Effects 0.000 description 3
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 229940106681 chloroacetic acid Drugs 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229960005215 dichloroacetic acid Drugs 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
- 235000021588 free fatty acids Nutrition 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- BZANQLIRVMZFOS-ZKZCYXTQSA-N (3r,4s,5s,6r)-2-butoxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound CCCCOC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O BZANQLIRVMZFOS-ZKZCYXTQSA-N 0.000 description 1
- SZSSMFVYZRQGIM-UHFFFAOYSA-N 2-(hydroxymethyl)-2-propylpropane-1,3-diol Chemical compound CCCC(CO)(CO)CO SZSSMFVYZRQGIM-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 101001061807 Homo sapiens Rab-like protein 6 Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 102000015636 Oligopeptides Human genes 0.000 description 1
- 108010038807 Oligopeptides Proteins 0.000 description 1
- 102100029618 Rab-like protein 6 Human genes 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/18—Quaternary ammonium compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/12—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of acyclic carbon skeletons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/221—Mono, di- or trisaccharides or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2065—Polyhydric alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
- - Alkylenglycole, wie beispielsweise Ethylenglycol, Diethylenglycol, Propylenglycol;
- - technische Oligoglyceringemische mit einem Eigenkondensationsgrad von 1,5 bis 10, wie etwa technische Diglyceringemische mit einem Diglyceringehalt von 40 bis 50 Gew.-%;
- - Methylolverbindungen, wie insbesondere Trimethylolethan, Trimethylolpropan, Trimethylolbutan, Pentaerythrit und Dipentaerythrit;
- - Niedrigalkylglucoside, insbesondere solche, mit 1 bis 8 Kohlenstoffen im Alkylrest wie beispiels weise Methyl- und Butylglucosid;
- - Zuckeralkohole mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Sorbit oder Mannit,
- - Zucker mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Glucose oder Saccharose;
- - Aminozucker, wie beispielsweise Glucamin.
Claims (10)
in der R1 für einen aliphatischen Alkylrest mit 6 bis 22 Kohlenstoffatomen, R2 und R3 unabhängig voneinander für einen Alkyl- oder Hydroxyalkylrest mit 1 bis 4 Kohlenstoffatomen und n für Zahlen im Bereich von 1 bis 3 steht, erhältlich durch Kondensation von tertiären Fettaminen mit Halogen carbonsäuresalzen in Gegenwart von Verflüssigungsmitteln sowie anschließender Drucknachbe handlung bei einer Temperatur von 110 bis 130°C und einem pH-Wert von 10 bis 14, dadurch ge kennzeichnet, daß sie als Verflüssigungsmittel einen Gehalt an Polyolverbindungen aufweisen, die ausgewählt sind aus der Gruppe, die von Alkylenglycolen, Oligoglyceringemischen, Methylol verbindungen, Niedrigalkylglucosiden, Zuckeralkoholen, Zuckern und Aminozuckern gebildet wird.
in der R1 für einen aliphatischen Alkylrest mit 6 bis 22 Kohlenstoffatomen und R2 und R3 unabhängig voneinander für Alkyl- oder Hydroxyalkylreste mit 1 bis 4 Kohlenstoffatomen stehen, mit Halogencarbonsäuren bzw. deren Salzen der Formel (III) kondensiert,
X-(CH2)nCOOY (III)
in der X für ein Halogen, Y für Wasserstoff oder ein Alkalimetall und m für Zahlen im Bereich von 1 bis 3 steht und anschließend einer Drucknachbehandlung bei Temperaturen im Bereich von 100 bis 130°C und einem pH-Wert von 10 bis 14 unterwirft, dadurch gekennzeichnet, daß man die Kondensationsreaktion in Gegenwart von Polyolverbindungen als Verflüssigungsmittel durchführt, die ausgewählt sind aus der Gruppe, die gebildet wird von Alkylenglycolen, Oligoglyceringe mischen, Methylolverbindungen, Niedrigalkylglucosiden, Zuckeralkoholen, Zuckern und Aminozu ckern.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19738634A DE19738634A1 (de) | 1997-09-04 | 1997-09-04 | Niedrigviskose wäßrige Konzentrate von Alkylbetainen |
FR9811020A FR2769017B1 (fr) | 1997-09-04 | 1998-09-03 | Concentres aqueux d'alkyl-betaine basse viscosite |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19738634A DE19738634A1 (de) | 1997-09-04 | 1997-09-04 | Niedrigviskose wäßrige Konzentrate von Alkylbetainen |
Publications (1)
Publication Number | Publication Date |
---|---|
DE19738634A1 true DE19738634A1 (de) | 1999-03-11 |
Family
ID=7841154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19738634A Ceased DE19738634A1 (de) | 1997-09-04 | 1997-09-04 | Niedrigviskose wäßrige Konzentrate von Alkylbetainen |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE19738634A1 (de) |
FR (1) | FR2769017B1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1338644A1 (de) * | 2002-02-23 | 2003-08-27 | Clariant GmbH | Hochkonzentrierte wässrige Lösungen von Betainen oder Aminoxiden |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2129264A (en) * | 1935-03-29 | 1938-09-06 | Du Pont | Nitrogen-containing organic compounds |
CH540295A (fr) * | 1972-01-05 | 1973-08-15 | Maggi Ag | Procédé de séparation de la bétaïne d'une solution aqueuse contenant des impuretés |
DE4408228C2 (de) * | 1994-03-11 | 1997-02-20 | Henkel Kgaa | Verfahren zur Herstellung niedrigviskoser wäßriger Betaintensidkonzentrate |
-
1997
- 1997-09-04 DE DE19738634A patent/DE19738634A1/de not_active Ceased
-
1998
- 1998-09-03 FR FR9811020A patent/FR2769017B1/fr not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1338644A1 (de) * | 2002-02-23 | 2003-08-27 | Clariant GmbH | Hochkonzentrierte wässrige Lösungen von Betainen oder Aminoxiden |
US7033989B2 (en) | 2002-02-23 | 2006-04-25 | Goldschmidt Gmbh | High-concentration aqueous solutions of betaines or amine oxides |
Also Published As
Publication number | Publication date |
---|---|
FR2769017A1 (fr) | 1999-04-02 |
FR2769017B1 (fr) | 2002-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0302329B1 (de) | Verfahren zur Herstellung konzentrierter fliessfähiger wässriger Lösungen von Betainen | |
EP0560114B1 (de) | Wässrige flüssige Lösung eines Betains mit mindestens 40 Gew.-% Festkörpergehalt | |
DE3613944C1 (de) | Verfahren zur Herstellung einer hochkonzentrierten,fliess- und pumpfaehigen Betainloesung | |
DE69433755T3 (de) | Verfahren zur Herstellung von Imidazolin abgeleiteten Amphoacetat-Tensiden von höherer Reinheit | |
EP0563747B1 (de) | Verfahren zur Herstellung von wässrigen Betainlösungen | |
DE3826654C1 (de) | ||
EP0730572B1 (de) | Niedrigviskose wässrige konzentrate von betaintensiden | |
EP0656346B1 (de) | Verfahren zur Herstellung hochkonzentrierter fliessfähiger wässriger Lösungen von Betainen | |
DE4435495C2 (de) | Pumpfähige wäßrige Tensidkonzentrate | |
DE69512895T2 (de) | Taurinderivate zur verwendung in reinigungsmittelzusammensetzungen | |
EP0647613B1 (de) | Verfahren zur Herstellung hochkonzentrierter fliessfähiger wässriger Lösungen von Betainen | |
DE19505196C1 (de) | Niedrigviskose wäßrige Konzentrate von Betaintensiden | |
DE19607824A1 (de) | Niedrigschmelzende Esterquats | |
EP0749412B1 (de) | Niedrigviskose wässrige konzentrate von betaintensiden | |
EP0452349B1 (de) | Verfahren zur herstellung von amphoteren grenzflächenaktiven imidazolinderivaten | |
DE19738634A1 (de) | Niedrigviskose wäßrige Konzentrate von Alkylbetainen | |
DE4408228A1 (de) | Niedrigviskose wäßrige Konzentrate von Betaintensiden | |
EP0739878B1 (de) | Verfahren zur Herstellung hochkonzentrierter fliessfähiger wässriger Lösungen von Betainen | |
EP0812821B1 (de) | Kohlensäureesterbetaine und deren Herstellung und Verwendung | |
EP0688311B1 (de) | Verfahren zur nachbehandlung von betainen und amphoteren tensiden | |
DE19523477C2 (de) | Verfahren zur Herstellung wäßriger, niedrigviskoser Betainkonzentrate | |
DE19503279C2 (de) | Kation- und/oder Amphooligomere | |
DE4337324C2 (de) | Verfahren zur Herstellung von Detergensgemischen | |
DE19527708A1 (de) | Verfahren zur Herstellung von Polyhydroxyfettsäureamid-Lösungen mit guter Farbqualität und deren Verwendung | |
DE19545134C2 (de) | Verfahren zur Herstellung hellfarbiger Betaine |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8127 | New person/name/address of the applicant |
Owner name: COGNIS DEUTSCHLAND GMBH, 40589 DUESSELDORF, DE SID |
|
8127 | New person/name/address of the applicant |
Owner name: COGNIS DEUTSCHLAND GMBH & CO. KG, 40589 DUESSELDOR |
|
8110 | Request for examination paragraph 44 | ||
8127 | New person/name/address of the applicant |
Owner name: COGNIS DEUTSCHLAND GMBH & CO. KG, 40589 DUESSELDORF Owner name: COGNIS FRANCE S.A., BOUSSENS, FR |
|
8127 | New person/name/address of the applicant |
Owner name: COGNIS IP MANAGEMENT GMBH, 40589 DUESSELDORF, DE Owner name: COGNIS FRANCE S.A., BOUSSENS, FR |
|
8128 | New person/name/address of the agent |
Representative=s name: REINHARDT, J., DIPL.-CHEM. DR. RER. NAT., PAT.-ASS |
|
8127 | New person/name/address of the applicant |
Owner name: COGNIS DEUTSCHLAND GMBH & CO. KG, 40589 DUESSELDORF Owner name: COGNIS FRANCE, S.A.S., BOUSSENS, FR |
|
8127 | New person/name/address of the applicant |
Owner name: COGNIS IP MANAGEMENT GMBH, 40589 DUESSELDORF, DE Owner name: COGNIS FRANCE, S.A.S., BOUSSENS, FR |
|
8131 | Rejection |