NL193247C - Fosforhoudende betaïnederivaten. - Google Patents

Fosforhoudende betaïnederivaten. Download PDF

Info

Publication number: NL193247C
Authority: NL; Netherlands
Prior art keywords: parts; carbon atoms; temperature; formula; added
Prior art date: 1978-05-05

Application number

NL7903526A

Other languages

English (en)

Dutch (nl)

Other versions

NL193247B (nl

NL7903526A (nl

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

1999-04-02

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

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

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

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

1979-11-07 Publication of NL7903526A publication Critical patent/NL7903526A/xx

1998-12-01 Publication of NL193247B publication Critical patent/NL193247B/xx

1999-04-02 Application granted granted Critical

1999-04-02 Publication of NL193247C publication Critical patent/NL193247C/nl

Links

OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims description 5
229910052698 phosphorus Inorganic materials 0.000 title claims description 5
239000011574 phosphorus Substances 0.000 title claims description 5
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 title 1
238000006243 chemical reaction Methods 0.000 claims description 230
125000004432 carbon atom Chemical group C* 0.000 claims description 127
238000003756 stirring Methods 0.000 claims description 108
125000000217 alkyl group Chemical group 0.000 claims description 101
239000007864 aqueous solution Substances 0.000 claims description 60
239000011874 heated mixture Substances 0.000 claims description 41
-1 2-chloroethoxyethoxy Chemical group 0.000 claims description 27
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 24
150000001875 compounds Chemical class 0.000 claims description 23
239000000203 mixture Substances 0.000 claims description 22
239000000376 reactant Substances 0.000 claims description 20
239000002253 acid Substances 0.000 claims description 18
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical class C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 14
229910052757 nitrogen Inorganic materials 0.000 claims description 14
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 12
239000008234 soft water Substances 0.000 claims description 12
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
125000003342 alkenyl group Chemical group 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000002947 alkylene group Chemical group 0.000 claims description 7
150000001450 anions Chemical class 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 6
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 5
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 5
125000000753 cycloalkyl group Chemical group 0.000 claims description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims description 4
229920000137 polyphosphoric acid Polymers 0.000 claims description 4
150000003839 salts Chemical group 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 3
150000001340 alkali metals Chemical class 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
125000004430 oxygen atom Chemical group O* 0.000 claims description 3
239000011541 reaction mixture Substances 0.000 claims description 3
150000001342 alkaline earth metals Chemical class 0.000 claims description 2
125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
125000006413 ring segment Chemical group 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
LAMUXTNQCICZQX-UHFFFAOYSA-N 3-chloropropan-1-ol Chemical compound OCCCCl LAMUXTNQCICZQX-UHFFFAOYSA-N 0.000 claims 1
SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 claims 1
239000000047 product Substances 0.000 description 111
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 53
229910001504 inorganic chloride Inorganic materials 0.000 description 51
238000010438 heat treatment Methods 0.000 description 48
150000003512 tertiary amines Chemical class 0.000 description 32
239000000243 solution Substances 0.000 description 28
238000004458 analytical method Methods 0.000 description 27
239000003153 chemical reaction reagent Substances 0.000 description 16
239000000543 intermediate Substances 0.000 description 15
239000006260 foam Substances 0.000 description 12
150000001412 amines Chemical group 0.000 description 11
238000002360 preparation method Methods 0.000 description 11
229910019142 PO4 Inorganic materials 0.000 description 10
239000010452 phosphate Substances 0.000 description 10
DUXYWXYOBMKGIN-UHFFFAOYSA-N trimyristin Chemical compound CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCC DUXYWXYOBMKGIN-UHFFFAOYSA-N 0.000 description 10
230000007794 irritation Effects 0.000 description 9
238000000034 method Methods 0.000 description 9
125000004122 cyclic group Chemical group 0.000 description 8
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 6
239000000463 material Substances 0.000 description 6
239000004166 Lanolin Substances 0.000 description 5
239000008367 deionised water Substances 0.000 description 5
229910021641 deionized water Inorganic materials 0.000 description 5
229940039717 lanolin Drugs 0.000 description 5
235000019388 lanolin Nutrition 0.000 description 5
BMZTZTSBZWUIKG-UHFFFAOYSA-N n-[3-(diethylamino)propyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NCCCN(CC)CC BMZTZTSBZWUIKG-UHFFFAOYSA-N 0.000 description 5
TWMFGCHRALXDAR-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]dodecanamide Chemical compound CCCCCCCCCCCC(=O)NCCCN(C)C TWMFGCHRALXDAR-UHFFFAOYSA-N 0.000 description 5
150000008301 phosphite esters Chemical class 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
206010015946 Eye irritation Diseases 0.000 description 4
241000283973 Oryctolagus cuniculus Species 0.000 description 4
229960003237 betaine Drugs 0.000 description 4
125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 description 4
231100000013 eye irritation Toxicity 0.000 description 4
GGBYJQDXDMGQAZ-UHFFFAOYSA-N n-[3-(diethylamino)propyl]tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCCCN(CC)CC GGBYJQDXDMGQAZ-UHFFFAOYSA-N 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000005187 foaming Methods 0.000 description 3
150000004820 halides Chemical class 0.000 description 3
VMPHSYLJUKZBJJ-UHFFFAOYSA-N lauric acid triglyceride Natural products CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 3
IFYDWYVPVAMGRO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)NCCCN(C)C IFYDWYVPVAMGRO-UHFFFAOYSA-N 0.000 description 3
239000011734 sodium Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 description 2
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
FOUZISDNESEYLX-UHFFFAOYSA-N N-hydroxyethyl glycine Natural products OCCNCC(O)=O FOUZISDNESEYLX-UHFFFAOYSA-N 0.000 description 2
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
125000002636 imidazolinyl group Chemical group 0.000 description 2
238000009434 installation Methods 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
DOKHEARVIDLSFF-UHFFFAOYSA-N prop-1-en-1-ol Chemical group CC=CO DOKHEARVIDLSFF-UHFFFAOYSA-N 0.000 description 2
FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
235000019333 sodium laurylsulphate Nutrition 0.000 description 2
239000012085 test solution Substances 0.000 description 2
239000002888 zwitterionic surfactant Substances 0.000 description 2
UCWYGNTYSWIDSW-QXMHVHEDSA-N (z)-n-[3-(dimethylamino)propyl]octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCCN(C)C UCWYGNTYSWIDSW-QXMHVHEDSA-N 0.000 description 1
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
241000700199 Cavia porcellus Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
BYMMIQCVDHHYGG-UHFFFAOYSA-N Cl.OP(O)(O)=O Chemical compound Cl.OP(O)(O)=O BYMMIQCVDHHYGG-UHFFFAOYSA-N 0.000 description 1
208000006069 Corneal Opacity Diseases 0.000 description 1
231100000635 Draize test Toxicity 0.000 description 1
XSISQURPIRTMAY-UHFFFAOYSA-N Hydroxyethyl glycine Chemical compound NCC(=O)OCCO XSISQURPIRTMAY-UHFFFAOYSA-N 0.000 description 1
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 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
206010040880 Skin irritation Diseases 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 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
239000003513 alkali Substances 0.000 description 1
229940031955 anhydrous lanolin Drugs 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000004140 cleaning Methods 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
229940073507 cocamidopropyl betaine Drugs 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
210000000795 conjunctiva Anatomy 0.000 description 1
210000004087 cornea Anatomy 0.000 description 1
231100000269 corneal opacity Toxicity 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
239000001177 diphosphate Substances 0.000 description 1
XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical class [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
235000011180 diphosphates Nutrition 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
210000000554 iris Anatomy 0.000 description 1
230000003902 lesion Effects 0.000 description 1
238000000622 liquid--liquid extraction Methods 0.000 description 1
FHHIIVLWHCTMBB-UHFFFAOYSA-N n-[3-(diethylamino)propyl]hexanamide Chemical compound CCCCCC(=O)NCCCN(CC)CC FHHIIVLWHCTMBB-UHFFFAOYSA-N 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
ACKIXIAOJWRZJJ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]hexanamide Chemical compound CCCCCC(=O)NCCCN(C)C ACKIXIAOJWRZJJ-UHFFFAOYSA-N 0.000 description 1
RZJGTTOKUNMVCJ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]octanamide Chemical compound CCCCCCCC(=O)NCCCN(C)C RZJGTTOKUNMVCJ-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000010979 pH adjustment Methods 0.000 description 1
239000000575 pesticide Substances 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
150000003014 phosphoric acid esters Chemical class 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
231100000475 skin irritation Toxicity 0.000 description 1
239000000344 soap Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000000638 solvent extraction Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004753 textile Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc 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)
Molecular Biology (AREA)
Biochemistry (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)
Cosmetics (AREA)
Detergent Compositions (AREA)

NL7903526A 1978-05-05 1979-05-04 Fosforhoudende betaïnederivaten. NL193247C (nl)

Applications Claiming Priority (6)

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
US90212178		1978-05-05
US96546178		1978-11-30
US96546278		1978-11-30
US05/965,462 US4261911A (en)	1978-11-30	1978-11-30	Phosphitaines
US05/965,461 US4215064A (en)	1978-11-30	1978-11-30	Phosphobetaines

Publications (3)

Publication Number	Publication Date
NL7903526A NL7903526A (nl)	1979-11-07
NL193247B NL193247B (nl)	1998-12-01
NL193247C true NL193247C (nl)	1999-04-02

Family

ID=27420590

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL7903526A NL193247C (nl)	1978-05-05	1979-05-04	Fosforhoudende betaïnederivaten.

Country Status (16)

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

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 (en) *	1973-04-09	1978-09-19	Robert J. Verdicchio	Amphoteric surface active agents
CH597252A5 (de) *	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 MX MX177513A patent/MX150948A/es unknown
- 1979-05-03 NZ NZ190363A patent/NZ190363A/xx unknown
- 1979-05-04 AT AT0335679A patent/AT376685B/de active
- 1979-05-04 BE BE0/195007A patent/BE876055A/xx not_active IP Right Cessation
- 1979-05-04 BR BR7902725A patent/BR7902725A/pt unknown
- 1979-05-04 FR FR7911364A patent/FR2424925B1/fr not_active Expired
- 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 PT PT69574A patent/PT69574A/pt unknown
- 1979-05-04 GR GR59021A patent/GR64909B/el unknown
- 1979-05-04 NL NL7903526A patent/NL193247C/nl not_active IP Right Cessation
- 1979-05-04 CH CH4206/79A patent/CH650001A5/de not_active IP Right Cessation
- 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
GR64909B (en)	1980-06-07
IE48107B1 (en)	1984-10-03
AR228016A1 (es)	1983-01-14
IE790881L (en)	1979-11-05
AT376685B (de)	1984-12-27
PH16742A (en)	1984-02-10
MX150948A (es)	1984-08-24
PT69574A (en)	1979-06-01
CH650001A5 (de)	1985-06-28
AU4693379A (en)	1979-11-08
AU528547B2 (en)	1983-05-05
NZ190363A (en)	1981-05-01
ATA335679A (de)	1984-05-15
GB2020289B (en)	1983-01-12
BR7902725A (pt)	1979-11-20
BE876055A (fr)	1979-11-05
NL193247B (nl)	1998-12-01
ES480266A1 (es)	1980-08-16
GB2020289A (en)	1979-11-14
NL7903526A (nl)	1979-11-07
FR2424925A1 (fr)	1979-11-30
FR2424925B1 (fr)	1988-05-20

Legal Events

Date	Code	Title	Description
1985-01-01	A85	Still pending on 85-01-01
1986-05-01	BA	A request for search or an international-type search has been filed
1986-07-01	BB	A search report has been drawn up
1986-11-03	BC	A request for examination has been filed
1999-07-01	V4	Discontinued because of reaching the maximum lifetime of a patent	Free format text: 19990504

Publication	Publication Date	Title
US4215064A (en)	1980-07-29	Phosphobetaines
US4380637A (en)	1983-04-19	Imidazoline phosphobetaines
US4209449A (en)	1980-06-24	Phosphate quaternary compounds
US4382036A (en)	1983-05-03	Pyrophosphobetaines
US4617414A (en)	1986-10-14	Process for the preparation of phosphate surfactants
US4137191A (en)	1979-01-30	Low-irritant surfactant composition
US5091493A (en)	1992-02-25	Silicone phosphobetaines
EP2643332B1 (de)	2014-10-22	Verfahren zur pufferung einer chemischen oder biologischen zusammensetzung
CA1132990A (en)	1982-10-05	Process for preparation of novel phosphorus containing surface active agents
US2073100A (en)	1937-03-09	Nu-aminoalkylamides of nu-alkyl-aminobenzoic acids and process of preparing them
US4269730A (en)	1981-05-26	Substituted imidazoline reactions with chloroacetate salts
US4261911A (en)	1981-04-14	Phosphitaines
JPS6171830A (ja)	1986-04-12	界面活性剤組成物
US5256805A (en)	1993-10-26	Silicone amido amine salts
CA1044913A (en)	1978-12-26	Method for increasing the sucrose content of growing plants
US6683033B2 (en)	2004-01-27	Concentrated aqueous betaine surfactant compositions and process for their preparation
US4304910A (en)	1981-12-08	Quarnary ammonium polymeric anti-microbial agent
ES484571A1 (es)	1980-05-16	Procedimiento para la obtencion de compuestos de n-oxaciclil-alquil-piperidil-diaza
US4336385A (en)	1982-06-22	Phosphate imidazolinium compounds
US4243602A (en)	1981-01-06	Novel quaternary compounds
US5156837A (en)	1992-10-20	Cosmetic compositions containing quaternized nitrogen compounds
JPS6340798B2 (de)	1988-08-12
US2471621A (en)	1949-05-31	Mercury compounds and process of making same
US4336386A (en)	1982-06-22	Quaternary imidazolinium phosphite derivatives
IE48107B1 (en)	1984-10-03	Novel betaine derivatives