JPS648634B2 - - Google Patents

Info

Publication number: JPS648634B2
Authority: JP; Japan
Prior art keywords: formula; compound; alkyl; reaction; compound according
Prior art date: 1979-07-23
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.): Expired

Application number

JP55099449A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5622791A (en

Inventor

Kee Oo Rindeman Maatein

Aaru Ruukenbatsuku Eruin

Jee Uerudeitsukio Robaato

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

JONSON ENDO JONSON BEIBII PURODAKUTSU CO

Original Assignee

JONSON ENDO JONSON BEIBII PURODAKUTSU CO

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.)

1979-07-23

Filing date

1980-07-22

Publication date

1989-02-14

1980-07-22 Application filed by JONSON ENDO JONSON BEIBII PURODAKUTSU CO filed Critical JONSON ENDO JONSON BEIBII PURODAKUTSU CO

1981-03-03 Publication of JPS5622791A publication Critical patent/JPS5622791A/ja

1989-02-14 Publication of JPS648634B2 publication Critical patent/JPS648634B2/ja

Status Granted legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 claims description 36
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 12
125000002947 alkylene group Chemical group 0.000 claims description 11
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 10
238000000034 method Methods 0.000 claims description 10
229910052736 halogen Inorganic materials 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 7
229910019142 PO4 Inorganic materials 0.000 claims description 5
239000010452 phosphate Substances 0.000 claims description 5
150000003512 tertiary amines Chemical class 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims 2
238000004519 manufacturing process Methods 0.000 claims 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
229910052698 phosphorus Inorganic materials 0.000 claims 1
239000011574 phosphorus Substances 0.000 claims 1
239000000203 mixture Substances 0.000 description 27
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 26
238000006243 chemical reaction Methods 0.000 description 26
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
239000011541 reaction mixture Substances 0.000 description 14
-1 halogen ions Chemical class 0.000 description 13
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 13
238000012360 testing method Methods 0.000 description 12
239000000047 product Substances 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 9
210000004209 hair Anatomy 0.000 description 8
239000004744 fabric Substances 0.000 description 7
238000003756 stirring Methods 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
238000001461 argentometric titration Methods 0.000 description 6
238000001816 cooling Methods 0.000 description 6
238000010992 reflux Methods 0.000 description 6
238000005406 washing Methods 0.000 description 6
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 5
238000004140 cleaning Methods 0.000 description 5
238000001035 drying Methods 0.000 description 5
239000011521 glass Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
239000008367 deionised water Substances 0.000 description 4
229910021641 deionized water Inorganic materials 0.000 description 4
239000003205 fragrance Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
238000001953 recrystallisation Methods 0.000 description 4
239000002904 solvent Substances 0.000 description 4
SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000000844 anti-bacterial effect Effects 0.000 description 3
238000009835 boiling Methods 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000006071 cream Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000001914 filtration Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000002453 shampoo Substances 0.000 description 3
150000005691 triesters Chemical class 0.000 description 3
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 2
WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
230000003385 bacteriostatic effect Effects 0.000 description 2
230000003750 conditioning effect Effects 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 2
229950010007 dimantine Drugs 0.000 description 2
238000004821 distillation Methods 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
BKRJTJJQPXVRRY-UHFFFAOYSA-M dodecyl-(2-hydroxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCO BKRJTJJQPXVRRY-UHFFFAOYSA-M 0.000 description 2
CWILBLFCNWVURT-UHFFFAOYSA-N n,n-diethylethanamine;octadecanamide Chemical compound CCN(CC)CC.CCCCCCCCCCCCCCCCCC(N)=O CWILBLFCNWVURT-UHFFFAOYSA-N 0.000 description 2
YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
239000003755 preservative agent Substances 0.000 description 2
238000005956 quaternization reaction Methods 0.000 description 2
238000000967 suction filtration Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000004448 titration Methods 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
CSHOPPGMNYULAD-UHFFFAOYSA-N 1-tridecoxytridecane Chemical compound CCCCCCCCCCCCCOCCCCCCCCCCCCC CSHOPPGMNYULAD-UHFFFAOYSA-N 0.000 description 1
JECYNCQXXKQDJN-UHFFFAOYSA-N 2-(2-methylhexan-2-yloxymethyl)oxirane Chemical class CCCCC(C)(C)OCC1CO1 JECYNCQXXKQDJN-UHFFFAOYSA-N 0.000 description 1
YJHSJERLYWNLQL-UHFFFAOYSA-N 2-hydroxyethyl(dimethyl)azanium;chloride Chemical compound Cl.CN(C)CCO YJHSJERLYWNLQL-UHFFFAOYSA-N 0.000 description 1
QOLLYDAQOZBRAL-UHFFFAOYSA-M 2-hydroxyethyl-dimethyl-octadecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCO QOLLYDAQOZBRAL-UHFFFAOYSA-M 0.000 description 1
238000009631 Broth culture Methods 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 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
150000001298 alcohols Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000002280 amphoteric surfactant Substances 0.000 description 1
ALYNCZNDIQEVRV-UHFFFAOYSA-N aniline-p-carboxylic acid Natural products NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000004599 antimicrobial Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
238000003556 assay Methods 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
239000000022 bacteriostatic agent Substances 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
238000009960 carding Methods 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
229960001927 cetylpyridinium chloride Drugs 0.000 description 1
YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
239000003599 detergent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
230000009881 electrostatic interaction Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000004434 industrial solvent Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
ICZKASVWFUJTEI-UHFFFAOYSA-N n,n-dimethyldocosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCN(C)C ICZKASVWFUJTEI-UHFFFAOYSA-N 0.000 description 1
AYNZRGVSQNDHIX-UHFFFAOYSA-N n,n-dimethylicosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN(C)C AYNZRGVSQNDHIX-UHFFFAOYSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
150000003017 phosphorus Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229940093429 polyethylene glycol 6000 Drugs 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
229910052709 silver Inorganic materials 0.000 description 1
239000004332 silver Substances 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000004071 soot Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
239000001226 triphosphate Substances 0.000 description 1
235000011178 triphosphate Nutrition 0.000 description 1
239000006150 trypticase soy agar Substances 0.000 description 1
238000001291 vacuum drying Methods 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
- 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
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Wood Science & Technology (AREA)
Agronomy & Crop Science (AREA)
Engineering & Computer Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Pest Control & Pesticides (AREA)
Dentistry (AREA)
Birds (AREA)
Epidemiology (AREA)
Dermatology (AREA)
Cosmetics (AREA)
Detergent Compositions (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

JP9944980A 1979-07-23 1980-07-22 Phosphoric acid triester Granted JPS5622791A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US5983879A	1979-07-23	1979-07-23

Publications (2)

Publication Number	Publication Date
JPS5622791A JPS5622791A (en)	1981-03-03
JPS648634B2 true JPS648634B2 (es)	1989-02-14

Family

ID=22025612

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP9944980A Granted JPS5622791A (en)	1979-07-23	1980-07-22	Phosphoric acid triester

Country Status (18)

Country	Link
JP (1)	JPS5622791A (es)
KR (1)	KR850000076B1 (es)
AR (1)	AR228431A1 (es)
AU (1)	AU536481B2 (es)
BR (1)	BR8004564A (es)
CA (1)	CA1126750A (es)
DE (1)	DE3027943A1 (es)
ES (1)	ES8105740A1 (es)
FR (1)	FR2461715A1 (es)
GR (1)	GR70013B (es)
IN (1)	IN153525B (es)
IT (1)	IT8049277A0 (es)
MX (1)	MX5854E (es)
NZ (1)	NZ194289A (es)
PH (1)	PH17453A (es)
PT (1)	PT71585B (es)
ZA (1)	ZA804419B (es)
ZW (1)	ZW16980A1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3326230A1 (de) *	1983-07-21	1985-01-31	Henkel KGaA, 4000 Düsseldorf	Mittel zum waschen und spuelen von haaren
DE3409634A1 (de) *	1984-03-16	1985-09-19	Henkel KGaA, 4000 Düsseldorf	Phosphonsaeureester in haarbehandlungsmitteln
JPS6122096A (ja) *	1984-07-09	1986-01-30	Kao Corp	糖リン酸エステルおよびその製造方法
US5300494A (en) *	1986-06-06	1994-04-05	Union Carbide Chemicals & Plastics Technology Corporation	Delivery systems for quaternary and related compounds
ATE196592T1 (de) *	1991-10-28	2000-10-15	Dennis L Fost	Phospholipid-antimikrobielle zusammensetzungen
FR2725365B1 (fr) *	1994-10-07	1996-11-08	Oreal	Composition nettoyante et/ou demaquillante contenant un alcool et un compose phosphate
US5567427A (en) *	1995-03-17	1996-10-22	Helene Curtis, Inc.	Emulsified, low ph cosmetic compositions having improved stability
CN105968133B (zh) *	2016-05-18	2018-09-21	大连和田科技有限公司	一种磷酸酯季铵盐杀菌剂的制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4181634A (en) *	1977-06-17	1980-01-01	Johnson & Johnson	Mild cleansing compositions comprising an alkyleneoxylated bisquaternary ammonium compound and an anionic or amphoteric detergent such as a phosphobetaine
AR228016A1 (es) *	1978-05-05	1983-01-14	Johnson & Johnson	Compuesto del grupo de las fosfobetainas y fosfitainas,util como tensioactivo anfoterico y zwitterionico
EP0013713B1 (en) *	1978-11-30	1984-04-11	Mona Industries	Phosphorus containing surface active agents and their preparation
US4209449A (en) *	1978-11-30	1980-06-24	Mona Industries	Phosphate quaternary compounds

1980
- 1980-06-30 AU AU59762/80A patent/AU536481B2/en not_active Expired
- 1980-07-05 IN IN783/CAL/80A patent/IN153525B/en unknown
- 1980-07-09 NZ NZ194289A patent/NZ194289A/xx unknown
- 1980-07-14 KR KR1019800002803A patent/KR850000076B1/ko active
- 1980-07-16 FR FR8015682A patent/FR2461715A1/fr active Pending
- 1980-07-17 GR GR62484A patent/GR70013B/el unknown
- 1980-07-18 IT IT8049277A patent/IT8049277A0/it unknown
- 1980-07-21 CA CA356,655A patent/CA1126750A/en not_active Expired
- 1980-07-21 PT PT71585A patent/PT71585B/pt unknown
- 1980-07-22 JP JP9944980A patent/JPS5622791A/ja active Granted
- 1980-07-22 PH PH24323A patent/PH17453A/en unknown
- 1980-07-22 ES ES493597A patent/ES8105740A1/es not_active Expired
- 1980-07-22 ZA ZA00804419A patent/ZA804419B/xx unknown
- 1980-07-22 BR BR8004564A patent/BR8004564A/pt not_active IP Right Cessation
- 1980-07-22 AR AR281844A patent/AR228431A1/es active
- 1980-07-22 ZW ZW169/80A patent/ZW16980A1/xx unknown
- 1980-07-23 MX MX808930U patent/MX5854E/es unknown
- 1980-07-23 DE DE19803027943 patent/DE3027943A1/de active Granted

Also Published As

Publication number	Publication date
IN153525B (es)	1984-07-21
KR850000076B1 (ko)	1985-02-18
AU536481B2 (en)	1984-05-10
MX5854E (es)	1984-08-09
ES493597A0 (es)	1981-06-16
KR830003506A (ko)	1983-06-21
CA1126750A (en)	1982-06-29
GR70013B (es)	1982-07-23
PT71585A (en)	1980-09-01
DE3027943A1 (de)	1981-02-19
PT71585B (en)	1981-12-17
JPS5622791A (en)	1981-03-03
PH17453A (en)	1984-08-29
ZA804419B (en)	1982-02-24
DE3027943C2 (es)	1988-09-01
ES8105740A1 (es)	1981-06-16
AU5976280A (en)	1981-01-29
NZ194289A (en)	1982-09-07
FR2461715A1 (fr)	1981-02-06
ZW16980A1 (en)	1982-04-21
BR8004564A (pt)	1981-02-03
AR228431A1 (es)	1983-03-15
IT8049277A0 (it)	1980-07-18

Publication	Publication Date	Title
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