JP2003523930A5 - - Google Patents
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- Publication number
- JP2003523930A5 JP2003523930A5 JP2000574498A JP2000574498A JP2003523930A5 JP 2003523930 A5 JP2003523930 A5 JP 2003523930A5 JP 2000574498 A JP2000574498 A JP 2000574498A JP 2000574498 A JP2000574498 A JP 2000574498A JP 2003523930 A5 JP2003523930 A5 JP 2003523930A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- acid
- dialkyl
- quaternary
- oil
- 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
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- 239000000047 product Substances 0.000 description 10
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 7
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical group 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 150000001735 carboxylic acids Chemical group 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- 241001125048 Sardina Species 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- -1 triglycerides Chemical class 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- YUFFSWGQGVEMMI-JLNKQSITSA-N (7Z,10Z,13Z,16Z,19Z)-docosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(O)=O YUFFSWGQGVEMMI-JLNKQSITSA-N 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- 241000273930 Brevoortia tyrannus Species 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- 235000021294 Docosapentaenoic acid Nutrition 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 235000021353 Lignoceric acid Nutrition 0.000 description 1
- CQXMAMUUWHYSIY-UHFFFAOYSA-N Lignoceric acid Natural products CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(O)C=C1 CQXMAMUUWHYSIY-UHFFFAOYSA-N 0.000 description 1
- 241001072282 Limnanthes Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 description 1
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 235000020673 eicosapentaenoic acid Nutrition 0.000 description 1
- 229960005135 eicosapentaenoic acid Drugs 0.000 description 1
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 description 1
- IQLUYYHUNSSHIY-HZUMYPAESA-N eicosatetraenoic acid Chemical compound CCCCCCCCCCC\C=C\C=C\C=C\C=C\C(O)=O IQLUYYHUNSSHIY-HZUMYPAESA-N 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000037308 hair color Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 235000019508 mustard seed Nutrition 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 229940119224 salmon oil Drugs 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000010686 shark liver oil Substances 0.000 description 1
- 229940069764 shark liver oil Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- QZZGJDVWLFXDLK-UHFFFAOYSA-N tetracosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(O)=O QZZGJDVWLFXDLK-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10277998P | 1998-10-02 | 1998-10-02 | |
| US60/102,779 | 1998-10-02 | ||
| US09/409,203 US6388111B1 (en) | 1998-10-02 | 1999-09-30 | Dialkyl quats |
| US09/409,203 | 1999-09-30 | ||
| PCT/US1999/022916 WO2000020380A1 (en) | 1998-10-02 | 1999-10-01 | Dialkyl quaternary ammonium derivatives of oils, fatty acids, triglycerides and their use in personal care products |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003523930A JP2003523930A (ja) | 2003-08-12 |
| JP2003523930A5 true JP2003523930A5 (enExample) | 2008-11-20 |
| JP4307735B2 JP4307735B2 (ja) | 2009-08-05 |
Family
ID=26799723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000574498A Expired - Lifetime JP4307735B2 (ja) | 1998-10-02 | 1999-10-01 | 身体保護製品 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US6388111B1 (enExample) |
| EP (1) | EP1117634B1 (enExample) |
| JP (1) | JP4307735B2 (enExample) |
| AU (1) | AU6409899A (enExample) |
| DE (1) | DE69929811T2 (enExample) |
| WO (1) | WO2000020380A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6562328B2 (en) * | 2000-03-29 | 2003-05-13 | Croda, Inc. | Fatty quat based on ante-iso compounds |
| US6998113B1 (en) * | 2005-01-31 | 2006-02-14 | Aquea Scientific Corporation | Bodywashes containing additives |
| US7037513B1 (en) | 2005-01-31 | 2006-05-02 | Aquea Scientific Corporation | Bodywash additives |
| US7025952B1 (en) | 2005-01-31 | 2006-04-11 | Aquea Scientific Corporation | Methods of preparation and use of bodywashes containing additives |
| US7001592B1 (en) | 2005-01-31 | 2006-02-21 | Aquea Scientific Corporation | Sunscreen compositions and methods of use |
| US20080112904A1 (en) * | 2005-03-08 | 2008-05-15 | Daniel Henry Traynor | Sunscreen Compositions And Methods Of Use |
| AU2008254646A1 (en) * | 2007-05-21 | 2008-11-27 | Aquea Scientific Corporation | Highly charged microcapsules |
| CA2709534C (en) * | 2007-12-21 | 2016-06-28 | Huntsman Petrochemical Llc | Method of preparing amidoamine alkoxylates and compositions thereof |
| WO2013017401A1 (en) | 2011-08-02 | 2013-02-07 | Solvay Specialty Polymers Italy S.P.A. | (per)fluoropolymer composition |
| US11724134B2 (en) | 2012-11-06 | 2023-08-15 | CoLabs International Corporation | Compositions containing a cellulose derived capsule with a sunscreen active agent |
| US11707421B2 (en) | 2012-11-06 | 2023-07-25 | Colabs Int'l Corp. | Compositions containing a flexible derived capsule with an active agent |
| EP2916814B1 (en) | 2012-11-06 | 2020-02-12 | Colabs International Corporation | Composition containing a cellulose derived capsule with a sunscreen |
| US11491088B2 (en) | 2012-11-06 | 2022-11-08 | CoLabs International Corporation | Compositions containing a capsule with a moisturizing agent |
| US11690793B2 (en) | 2012-11-06 | 2023-07-04 | Colabs Int'l Corp. | Composition containing a cellulose derived capsule with a sunscreen |
| US10322301B2 (en) | 2012-11-06 | 2019-06-18 | CoLabs International Corporation | Compositions containing a cellulose derived capsule with a sunscreen active agent |
| PE20170265A1 (es) * | 2014-04-07 | 2017-03-26 | Epax Norway As | Composicion de acidos grasos monoinsaturados de cadena larga y metodo para la produccion de la misma |
| BR112019011016B1 (pt) * | 2016-12-01 | 2023-04-04 | Croda, Inc | Ingredientes para uso em composições para cuidados pessoais |
| WO2020006322A1 (en) | 2018-06-27 | 2020-01-02 | CoLabs International Corporation | Compositions comprising silicon dioxide-based particles including one or more agents |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4117107A (en) * | 1975-10-17 | 1978-09-26 | Noxell Corporation | Method and composition for improving oral hygiene |
| DE3638918A1 (de) | 1986-11-14 | 1988-05-26 | Henkel Kgaa | Quartaere ammoniumverbindungen, deren herstellung und verwendung als textilnachbehandlungsmittel |
| US4954335A (en) | 1989-05-31 | 1990-09-04 | Helene Curtis, Inc. | Clear conditioning composition and method to impart improved properties to the hair |
| US4976956A (en) | 1989-07-24 | 1990-12-11 | Helene Curtis, Inc. | Method and composition to impart improved conditioning properties to the hair |
| DE69105870T2 (de) * | 1990-08-23 | 1995-05-24 | Kao Corp., Tokio/Tokyo | Kationische Verbindung und Reinigungsmittelzusammensetzung. |
| US5525245A (en) | 1994-12-21 | 1996-06-11 | Colgate-Palmolive Company | Clear, concentrated liquid fabric softener compositions |
| WO1998017757A2 (en) | 1996-10-21 | 1998-04-30 | The Procter & Gamble Company | High usage of fabric softener compositions for improved benefits |
| WO1998017750A1 (en) | 1996-10-21 | 1998-04-30 | The Procter & Gamble Company | Concentrated, fabric softening composition |
| ES2126495B1 (es) * | 1996-11-05 | 1999-12-01 | Kao Corp Sa | Composiciones acuosas concentradas de tensioactivos del tipo de las betainas y su procedimiento de obtencion. |
| US5919958A (en) * | 1997-05-01 | 1999-07-06 | Fan Tech Ltd | Meadowfoam amidopropyl dimethyl amine salts |
| US5874395A (en) * | 1997-12-29 | 1999-02-23 | Colgate-Palmolive Company | Liquid rinse cycle fabric softening compositions containing diacid polymeric fatty ester quaternary ammonium compounds |
-
1999
- 1999-09-30 US US09/409,203 patent/US6388111B1/en not_active Expired - Lifetime
- 1999-10-01 JP JP2000574498A patent/JP4307735B2/ja not_active Expired - Lifetime
- 1999-10-01 WO PCT/US1999/022916 patent/WO2000020380A1/en not_active Ceased
- 1999-10-01 EP EP99951714A patent/EP1117634B1/en not_active Expired - Lifetime
- 1999-10-01 DE DE69929811T patent/DE69929811T2/de not_active Expired - Lifetime
- 1999-10-01 AU AU64098/99A patent/AU6409899A/en not_active Abandoned
-
2002
- 2002-03-15 US US10/098,932 patent/US6500791B2/en not_active Expired - Fee Related
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