CH650001A5 - Phosphobetainderivate und phosphotaine. - Google Patents

Phosphobetainderivate und phosphotaine. Download PDF

Info

Publication number: CH650001A5
Authority: CH; Switzerland
Prior art keywords: parts; alkyl; mixture; atoms; formula
Prior art date: 1978-05-05

Application number

CH4206/79A

Other languages

German (de)

English (en)

Inventor

Martin Lindemann

Raymond Mayhew

Anthony Jun O'lenick

Robert Verdicchio

Original Assignee

Johnson & Johnson

Mona Industries Inc

Priority date (The priority date 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 date listed.)

1978-05-05

Filing date

1979-05-04

Publication date

1985-06-28

1978-05-05 Priority claimed from US05/902,121 external-priority patent/US4181634A/en

1978-11-30 Priority claimed from US05/965,461 external-priority patent/US4215064A/en

1978-11-30 Priority claimed from US05/965,462 external-priority patent/US4261911A/en

1979-05-04 Application filed by Johnson & Johnson, Mona Industries Inc filed Critical Johnson & Johnson

1985-06-28 Publication of CH650001A5 publication Critical patent/CH650001A5/de

Links

239000000203 mixture Substances 0.000 claims description 117
125000000217 alkyl group Chemical group 0.000 claims description 61
125000004432 carbon atom Chemical group C* 0.000 claims description 44
150000001875 compounds Chemical class 0.000 claims description 44
229910052757 nitrogen Inorganic materials 0.000 claims description 26
-1 2-hydroxypropyl Chemical group 0.000 claims description 23
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 15
235000013162 Cocos nucifera Nutrition 0.000 claims description 12
244000060011 Cocos nucifera Species 0.000 claims description 12
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 6
150000001450 anions Chemical class 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
125000000400 lauroyl group Chemical group O=C([*])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])C([H])([H])[H] 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
150000002500 ions Chemical class 0.000 claims description 5
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
125000001419 myristoyl group Chemical group O=C([*])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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000003513 alkali Substances 0.000 claims description 3
150000001342 alkaline earth metals Chemical class 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
229910052717 sulfur Inorganic materials 0.000 claims description 3
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000005842 heteroatom Chemical group 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
125000004181 carboxyalkyl group Chemical group 0.000 claims 2
235000014113 dietary fatty acids Nutrition 0.000 claims 2
229930195729 fatty acid Natural products 0.000 claims 2
239000000194 fatty acid Substances 0.000 claims 2
150000004665 fatty acids Chemical class 0.000 claims 2
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
125000002877 alkyl aryl group Chemical group 0.000 claims 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
125000006413 ring segment Chemical group 0.000 claims 1
239000011593 sulfur Substances 0.000 claims 1
238000006243 chemical reaction Methods 0.000 description 145
239000000047 product Substances 0.000 description 110
238000003756 stirring Methods 0.000 description 104
239000007864 aqueous solution Substances 0.000 description 60
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 53
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 51
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 50
239000000126 substance Substances 0.000 description 50
229910001504 inorganic chloride Inorganic materials 0.000 description 49
239000000243 solution Substances 0.000 description 36
150000003512 tertiary amines Chemical class 0.000 description 28
239000011874 heated mixture Substances 0.000 description 23
239000002253 acid Substances 0.000 description 19
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical class C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 13
238000002360 preparation method Methods 0.000 description 12
239000008234 soft water Substances 0.000 description 11
150000001412 amines Chemical class 0.000 description 10
239000006260 foam Substances 0.000 description 10
229960003237 betaine Drugs 0.000 description 9
238000000034 method Methods 0.000 description 9
241000251730 Chondrichthyes Species 0.000 description 7
150000003014 phosphoric acid esters Chemical class 0.000 description 7
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
239000004166 Lanolin Substances 0.000 description 6
239000000543 intermediate Substances 0.000 description 6
229940039717 lanolin Drugs 0.000 description 6
235000019388 lanolin Nutrition 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
125000004122 cyclic group Chemical group 0.000 description 5
239000008367 deionised water Substances 0.000 description 5
229910021641 deionized water Inorganic materials 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
239000000376 reactant Substances 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
239000011734 sodium Substances 0.000 description 5
239000000080 wetting agent Substances 0.000 description 5
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
241000283973 Oryctolagus cuniculus Species 0.000 description 4
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 4
230000007794 irritation Effects 0.000 description 4
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 4
229920000137 polyphosphoric acid Polymers 0.000 description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
239000011575 calcium Substances 0.000 description 3
229910052802 copper Inorganic materials 0.000 description 3
238000005187 foaming Methods 0.000 description 3
150000004820 halides Chemical class 0.000 description 3
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
229910052698 phosphorus Inorganic materials 0.000 description 3
239000011574 phosphorus Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
206010015946 Eye irritation Diseases 0.000 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 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
FOUZISDNESEYLX-UHFFFAOYSA-N N-hydroxyethyl glycine Natural products OCCNCC(O)=O FOUZISDNESEYLX-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
229910000397 disodium phosphate Inorganic materials 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
231100000013 eye irritation Toxicity 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
238000011835 investigation Methods 0.000 description 2
230000000622 irritating effect Effects 0.000 description 2
239000000463 material Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000020477 pH reduction Effects 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
229910000162 sodium phosphate Inorganic materials 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
CPEONABTMRSIKA-UHFFFAOYSA-N 1,4$l^{2}-oxazinane Chemical compound C1COCC[N]1 CPEONABTMRSIKA-UHFFFAOYSA-N 0.000 description 1
YYTSGNJTASLUOY-UHFFFAOYSA-N 1-chloropropan-2-ol Chemical compound CC(O)CCl YYTSGNJTASLUOY-UHFFFAOYSA-N 0.000 description 1
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
SZMFCYVBKZAEPK-UHFFFAOYSA-N 3-hydroxy-2-methylpentadecanoic acid Chemical compound CCCCCCCCCCCCC(O)C(C)C(O)=O SZMFCYVBKZAEPK-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
241000283153 Cetacea Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
101150065749 Churc1 gene Proteins 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
231100000635 Draize test Toxicity 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
XSISQURPIRTMAY-UHFFFAOYSA-N Hydroxyethyl glycine Chemical compound NCC(=O)OCCO XSISQURPIRTMAY-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
102100038239 Protein Churchill Human genes 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
QHVSSYHBQAZXNZ-UHFFFAOYSA-N [C].OC=CC Chemical group [C].OC=CC QHVSSYHBQAZXNZ-UHFFFAOYSA-N 0.000 description 1
230000006978 adaptation Effects 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
229940031955 anhydrous lanolin Drugs 0.000 description 1
238000013459 approach Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
ITVPBBDAZKBMRP-UHFFFAOYSA-N chloro-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound OP(O)(Cl)=O ITVPBBDAZKBMRP-UHFFFAOYSA-N 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
210000004087 cornea Anatomy 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000010494 dissociation reaction Methods 0.000 description 1
230000005593 dissociations Effects 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940043264 dodecyl sulfate Drugs 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000001815 facial effect Effects 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
210000002837 heart atrium Anatomy 0.000 description 1
150000002462 imidazolines Chemical class 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
231100001032 irritation of the eye Toxicity 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
150000001455 metallic ions Chemical class 0.000 description 1
UKXSMVIDPJCDAQ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]benzamide Chemical compound CN(C)CCCNC(=O)C1=CC=CC=C1 UKXSMVIDPJCDAQ-UHFFFAOYSA-N 0.000 description 1
IFYDWYVPVAMGRO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCCCN(C)C IFYDWYVPVAMGRO-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
125000004437 phosphorous atom Chemical group 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
DOKHEARVIDLSFF-UHFFFAOYSA-N prop-1-en-1-ol Chemical group CC=CO DOKHEARVIDLSFF-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000523 sample Substances 0.000 description 1
239000012488 sample solution Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000002602 strong irritant Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
150000003511 tertiary amides Chemical class 0.000 description 1
239000012085 test solution Substances 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000002888 zwitterionic surfactant Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
- A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/1411—Esters of phosphorous acids with hydroxyalkyl compounds with further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6503—Five-membered rings
- C07F9/6506—Five-membered rings having the nitrogen atoms in positions 1 and 3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/6533—Six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65502—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a three-membered ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
- C07F9/6574—Esters of oxyacids of phosphorus
- C07F9/65742—Esters of oxyacids of phosphorus non-condensed with carbocyclic rings or heterocyclic rings or ring systems
- 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
- C11D1/38—Cationic compounds
- C11D1/62—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
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic 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
- C11D1/886—Ampholytes containing P
- 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
- C11D1/94—Mixtures with anionic, cationic or non-ionic 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
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic acids
- 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
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
- 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
- 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
- C11D1/92—Sulfobetaines ; Sulfitobetaines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Wood Science & Technology (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Epidemiology (AREA)
Birds (AREA)
Dermatology (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)
Cosmetics (AREA)
Detergent Compositions (AREA)

CH4206/79A 1978-05-05 1979-05-04 Phosphobetainderivate und phosphotaine. CH650001A5 (de)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US05/902,121 US4181634A (en)	1977-06-17	1978-05-05	Mild cleansing compositions comprising an alkyleneoxylated bisquaternary ammonium compound and an anionic or amphoteric detergent such as a phosphobetaine
US05/965,461 US4215064A (en)	1978-11-30	1978-11-30	Phosphobetaines
US05/965,462 US4261911A (en)	1978-11-30	1978-11-30	Phosphitaines

Publications (1)

Publication Number	Publication Date
CH650001A5 true CH650001A5 (de)	1985-06-28

Family

ID=27420590

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH4206/79A CH650001A5 (de)	1978-05-05	1979-05-04	Phosphobetainderivate und phosphotaine.

Country Status (16)

Country	Link
AR (1)	AR228016A1 (fr)
AT (1)	AT376685B (fr)
AU (1)	AU528547B2 (fr)
BE (1)	BE876055A (fr)
BR (1)	BR7902725A (fr)
CH (1)	CH650001A5 (fr)
ES (1)	ES480266A1 (fr)
FR (1)	FR2424925B1 (fr)
GB (1)	GB2020289B (fr)
GR (1)	GR64909B (fr)
IE (1)	IE48107B1 (fr)
MX (1)	MX150948A (fr)
NL (1)	NL193247C (fr)
NZ (1)	NZ190363A (fr)
PH (1)	PH16742A (fr)
PT (1)	PT69574A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU536481B2 (en) *	1979-07-23	1984-05-10	Johnson & Johnson Baby Products Company	Phosphoric acid triesters
US4617414A (en) *	1984-09-10	1986-10-14	Johnson & Johnson Baby Products Company	Process for the preparation of phosphate surfactants
JPH0725778B2 (ja) *	1987-10-21	1995-03-22	花王株式会社	リン酸エステル、その製造法およびそれを含有する洗浄剤組成物

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE792662A (fr) *	1971-12-13	1973-06-13	Hoechst Ag	Composes du phosphore qui sont des ions mixtes
CA1038766A (fr) *	1973-04-09	1978-09-19	Robert J. Verdicchio	Agents tensio-actifs amphoteres
CH597252A5 (fr) *	1973-04-14	1978-03-31	Hoechst Ag
US3950417A (en) *	1975-02-28	1976-04-13	Johnson & Johnson	High-lathering non-irritating detergent compositions

1979
- 1979-04-30 AR AR276345A patent/AR228016A1/es active
- 1979-05-03 NZ NZ190363A patent/NZ190363A/xx unknown
- 1979-05-03 MX MX177513A patent/MX150948A/es unknown
- 1979-05-04 CH CH4206/79A patent/CH650001A5/de not_active IP Right Cessation
- 1979-05-04 GR GR59021A patent/GR64909B/el unknown
- 1979-05-04 BR BR7902725A patent/BR7902725A/pt unknown
- 1979-05-04 AT AT0335679A patent/AT376685B/de active
- 1979-05-04 PT PT69574A patent/PT69574A/pt unknown
- 1979-05-04 GB GB7915709A patent/GB2020289B/en not_active Expired
- 1979-05-04 ES ES480266A patent/ES480266A1/es not_active Expired
- 1979-05-04 BE BE0/195007A patent/BE876055A/fr not_active IP Right Cessation
- 1979-05-04 NL NL7903526A patent/NL193247C/nl not_active IP Right Cessation
- 1979-05-04 FR FR7911364A patent/FR2424925B1/fr not_active Expired
- 1979-05-07 PH PH22510A patent/PH16742A/en unknown
- 1979-05-11 AU AU46933/79A patent/AU528547B2/en not_active Expired
- 1979-08-08 IE IE881/79A patent/IE48107B1/en not_active IP Right Cessation

Also Published As

Publication number	Publication date
IE48107B1 (en)	1984-10-03
IE790881L (en)	1979-11-05
NZ190363A (en)	1981-05-01
FR2424925B1 (fr)	1988-05-20
MX150948A (es)	1984-08-24
ES480266A1 (es)	1980-08-16
GB2020289A (en)	1979-11-14
AR228016A1 (es)	1983-01-14
BR7902725A (pt)	1979-11-20
PH16742A (en)	1984-02-10
GB2020289B (en)	1983-01-12
AU528547B2 (en)	1983-05-05
NL7903526A (nl)	1979-11-07
BE876055A (fr)	1979-11-05
FR2424925A1 (fr)	1979-11-30
NL193247C (nl)	1999-04-02
ATA335679A (de)	1984-05-15
AU4693379A (en)	1979-11-08
NL193247B (nl)	1998-12-01
GR64909B (en)	1980-06-07
AT376685B (de)	1984-12-27
PT69574A (en)	1979-06-01

Legal Events

Date	Code	Title	Description
1999-05-31	PL	Patent ceased

Publication	Publication Date	Title
DE69419601T2 (de)	1999-12-02	Aminderivate und sie enthaltende dermatologische zubereitungen
US4382036A (en)	1983-05-03	Pyrophosphobetaines
DE69011402T2 (de)	1994-12-15	Amidderivate und sie enthaltende Hautpräparationen.
EP0507337A2 (fr)	1992-10-07	Nouveaus dérivés dérucyle, brassidyle et nervonyle
DE69602809T2 (de)	1999-12-16	Transportvehikel für Makromoleküle
WO1994001406A1 (fr)	1994-01-20	Agents de contraste pour diagnostic rm
DE2339888A1 (de)	1974-02-21	Biologisch abbaubare sequestrantverbindung
DE1720009A1 (de)	1971-05-19	Verfahren zur Herstellung von 5-basisch substituierten 10,11-Dihydro-5H-dibenzo[b,e][1,4]diazepinen
DE2449445A1 (de)	1975-04-24	Verwendung von saeureamiden in waessrigen fluiden fuer die metallbearbeitung
EP0154977B1 (fr)	1989-05-17	Phosphatides de glycérine-éther, leur préparation et utilisation
CA1132990A (fr)	1982-10-05	Methode de preparation d'agents tensio-actifs nouveau genre a teneur de phosphore
CH650001A5 (de)	1985-06-28	Phosphobetainderivate und phosphotaine.
DE2752116C2 (de)	1984-07-12	Salze von N-[N',N'-Bis(2-carboxyethyl)-aminoethyl]-N-(2-hydroxyethyl)-carbonsäureamiden, Verfahren zu ihrer Herstellung und ihre Verwendung als grenzflächenaktive Stoffe
DE3789395T2 (de)	1994-08-04	Alkylendiamin-Derivate.
DE3027943C2 (fr)	1988-09-01
EP0373491A1 (fr)	1990-06-20	Procédé pour la préparation de dérivés d'imidazoline amphotères tensio-actifs
DE2828487A1 (de)	1979-01-18	Verfahren zur herstellung von 3-acylamino-4-homoisotwistan
DE3628916A1 (de)	1987-03-12	Phosphorsaeureester
DE3627280A1 (de)	1987-02-19	Verfahren zur herstellung von aminocarbonsaeuren vom saeuretyp
DE69523265T2 (de)	2002-07-04	Verfahren zur herstellung von phosphonsäure-derivaten
DE68918924T2 (de)	1995-05-18	Phosphorsäureester.
EP0265824A2 (fr)	1988-05-04	Phosphates tensioactifs amphotères et zwitterioniques
JP3833724B2 (ja)	2006-10-18	しわ改善剤
EP0354404B1 (fr)	1994-07-06	Bétaines phosphorées, leur procédé de préparation et leur utilisation, en particulier dans des buts industriels
DE1768277A1 (de)	1972-03-30	Aminoalkoholderivate