JPH0327556B2 - - Google Patents
Info
- Publication number
- JPH0327556B2 JPH0327556B2 JP61091704A JP9170486A JPH0327556B2 JP H0327556 B2 JPH0327556 B2 JP H0327556B2 JP 61091704 A JP61091704 A JP 61091704A JP 9170486 A JP9170486 A JP 9170486A JP H0327556 B2 JPH0327556 B2 JP H0327556B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- carbon atoms
- phosphoric acid
- groups
- 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.)
- Expired - Lifetime
Links
- -1 Phosphate ester Chemical class 0.000 claims description 32
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 150000007514 bases Chemical class 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 150000003973 alkyl amines Chemical class 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 54
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- 150000001875 compounds Chemical class 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 22
- 235000019441 ethanol Nutrition 0.000 description 19
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 150000003904 phospholipids Chemical class 0.000 description 14
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 13
- 239000000047 product Substances 0.000 description 11
- 238000001914 filtration Methods 0.000 description 9
- 238000004128 high performance liquid chromatography Methods 0.000 description 9
- 238000001816 cooling Methods 0.000 description 8
- 238000000921 elemental analysis Methods 0.000 description 8
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003012 bilayer membrane Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical group C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- VVLWBRGWQPWOJO-UHFFFAOYSA-M sodium;dodecyl oxiran-2-ylmethyl phosphate Chemical compound [Na+].CCCCCCCCCCCCOP([O-])(=O)OCC1CO1 VVLWBRGWQPWOJO-UHFFFAOYSA-M 0.000 description 3
- 125000000539 amino acid group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 210000000170 cell membrane Anatomy 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- UIEJMTYJRLFUAQ-UHFFFAOYSA-L disodium 3-chloropropyl phosphate Chemical compound [Na+].P(=O)(OCCCCl)([O-])[O-].[Na+] UIEJMTYJRLFUAQ-UHFFFAOYSA-L 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 125000001165 hydrophobic group Chemical group 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000003541 multi-stage reaction Methods 0.000 description 2
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- AVQQQFIHPOIRPM-UHFFFAOYSA-N (3-chloro-2-hydroxypropyl) dodecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(=O)OCC(O)CCl AVQQQFIHPOIRPM-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000002511 behenyl 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])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
- 230000004071 biological effect Effects 0.000 description 1
- 239000003876 biosurfactant Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000003493 decenyl group Chemical group [H]C([*])=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])[H] 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- VMDFYAXDCJPWNV-UHFFFAOYSA-L disodium oxiran-2-ylmethyl phosphate Chemical compound P(=O)(OCC1CO1)([O-])[O-].[Na+].[Na+] VMDFYAXDCJPWNV-UHFFFAOYSA-L 0.000 description 1
- 125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
- 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 1
- 229940079593 drug Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- MLTWWHUPECYSBZ-UHFFFAOYSA-N ethene-1,1,2-triol Chemical group OC=C(O)O MLTWWHUPECYSBZ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 125000002463 lignoceryl 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])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
- 239000002502 liposome Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 125000001802 myricyl 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])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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 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 1
- 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000000913 palmityl 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])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004713 phosphodiesters Chemical group 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FPVFIBUURAFKDE-UHFFFAOYSA-M sodium;(2-nonylphenyl) oxiran-2-ylmethyl phosphate Chemical compound [Na+].CCCCCCCCCC1=CC=CC=C1OP([O-])(=O)OCC1OC1 FPVFIBUURAFKDE-UHFFFAOYSA-M 0.000 description 1
- ZHSPPHBLBOYAGB-UHFFFAOYSA-M sodium;(3-chloro-2-hydroxypropyl) 1,1,2,2,3,3,4,4,5,5,6,6,7,7,10,10,10-heptadecafluorodecyl phosphate Chemical compound [Na+].ClCC(O)COP([O-])(=O)OC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CCC(F)(F)F ZHSPPHBLBOYAGB-UHFFFAOYSA-M 0.000 description 1
- KCBRUEFMEUHXBM-UHFFFAOYSA-M sodium;(3-chloro-2-hydroxypropyl) 1,1,2,2,3,3,4,4,5,5,6,6,7,7,12,12,12-heptadecafluorododecyl phosphate Chemical compound [Na+].ClCC(O)COP([O-])(=O)OC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CCCCC(F)(F)F KCBRUEFMEUHXBM-UHFFFAOYSA-M 0.000 description 1
- GBHXAZWFWMEHCO-UHFFFAOYSA-M sodium;(3-chloro-2-hydroxypropyl) 2-hexyldecyl phosphate Chemical compound [Na+].CCCCCCCCC(CCCCCC)COP([O-])(=O)OCC(O)CCl GBHXAZWFWMEHCO-UHFFFAOYSA-M 0.000 description 1
- JCCPEFUVYGYCDW-UHFFFAOYSA-M sodium;(3-chloro-2-hydroxypropyl) dodecyl phosphate Chemical compound [Na+].CCCCCCCCCCCCOP([O-])(=O)OCC(O)CCl JCCPEFUVYGYCDW-UHFFFAOYSA-M 0.000 description 1
- VVRPZZVUHAVSGP-UHFFFAOYSA-M sodium;1,1,2,2,3,3,4,4,5,5,6,6,7,7,10,10,10-heptadecafluorodecyl oxiran-2-ylmethyl phosphate Chemical compound [Na+].FC(F)(F)CCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)OP(=O)([O-])OCC1CO1 VVRPZZVUHAVSGP-UHFFFAOYSA-M 0.000 description 1
- XGMAINDUPQSERB-UHFFFAOYSA-M sodium;1,1,2,2,3,3,4,4,5,5,6,6,7,7,12,12,12-heptadecafluorododecyl oxiran-2-ylmethyl phosphate Chemical compound [Na+].FC(F)(F)CCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)OP(=O)([O-])OCC1CO1 XGMAINDUPQSERB-UHFFFAOYSA-M 0.000 description 1
- OVYTZAASVAZITK-UHFFFAOYSA-M sodium;ethanol;hydroxide Chemical compound [OH-].[Na+].CCO OVYTZAASVAZITK-UHFFFAOYSA-M 0.000 description 1
- BEPWQMRYWITZNI-UHFFFAOYSA-M sodium;octadec-1-enyl oxiran-2-ylmethyl phosphate Chemical compound [Na+].CCCCCCCCCCCCCCCCC=COP([O-])(=O)OCC1CO1 BEPWQMRYWITZNI-UHFFFAOYSA-M 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
Classifications
-
- 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 PâC bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
Description
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Claims (1)
- ãç¹èš±è«æ±ã®ç¯å²ã ïŒ äžè¬åŒïŒïŒã ïŒåŒäžãR1ã¯ççŽ æ°ïŒã36ã®çŽéãããã¯åå²
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Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61091704A JPS62249995A (ja) | 1986-04-21 | 1986-04-21 | ãªã³é žãšã¹ãã«ããã³ãã®è£œé æ³ |
| KR1019870002392A KR940011186B1 (ko) | 1986-04-21 | 1987-03-17 | ìžì° ìì€í 륎 ë° ê·žì ì ì¡°ë°©ë² |
| US07/032,627 US4845239A (en) | 1986-04-21 | 1987-04-01 | Phosphoric esters and process for preparing the same |
| MYPI87000458A MY101645A (en) | 1986-04-21 | 1987-04-09 | Phosphoric esters and process for preparing the same. |
| DE8787105556T DE3761140D1 (de) | 1986-04-21 | 1987-04-14 | Phosphorsaeureester und verfahren zu ihrer herstellung. |
| ES87105556T ES2015282B3 (es) | 1986-04-21 | 1987-04-14 | Esteres fosforicos y proceso para su preparacion. |
| EP87105556A EP0242781B1 (en) | 1986-04-21 | 1987-04-14 | Phosphoric esters and process for preparing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61091704A JPS62249995A (ja) | 1986-04-21 | 1986-04-21 | ãªã³é žãšã¹ãã«ããã³ãã®è£œé æ³ |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62249995A JPS62249995A (ja) | 1987-10-30 |
| JPH0327556B2 true JPH0327556B2 (ja) | 1991-04-16 |
Family
ID=14033900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61091704A Granted JPS62249995A (ja) | 1986-04-21 | 1986-04-21 | ãªã³é žãšã¹ãã«ããã³ãã®è£œé æ³ |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4845239A (ja) |
| EP (1) | EP0242781B1 (ja) |
| JP (1) | JPS62249995A (ja) |
| KR (1) | KR940011186B1 (ja) |
| DE (1) | DE3761140D1 (ja) |
| ES (1) | ES2015282B3 (ja) |
| MY (1) | MY101645A (ja) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0720987B2 (ja) * | 1987-10-21 | 1995-03-08 | è±çæ ªåŒäŒç€Ÿ | ããããããã³ã¿ã³ãã¯è³ªã®æ¹è³ªæ¹æ³ |
| JP2511706B2 (ja) * | 1988-12-22 | 1996-07-03 | è±çæ ªåŒäŒç€Ÿ | ãªã³é žãšã¹ãã« |
| DE60313425T2 (de) * | 2002-12-26 | 2008-01-03 | Kao Corp. | Verfahren zur Herstellung und zur Stabilisierung von Phosphaten |
| US20150266908A1 (en) * | 2012-09-26 | 2015-09-24 | Seung Min Kwak | Flame retardant comprising aromatic phosphate ester-based compound, and method for preparing same |
| KR101241148B1 (ko) * | 2012-09-26 | 2013-03-11 | 곜ì¹ë¯Œ | ë°©í¥ì¡± ìžì°ìì€í ë¥Žê³ íí©ë¬Œì í¬íší ë°©ìŒì ë° ê·žì ì ì¡°ë°©ë² |
| CN112522015B (zh) * | 2020-12-15 | 2022-12-06 | 广å·åœæºæ¶Šæ»ç§ææéå ¬åž | èºæåŒç©ºæ°å猩æºæ²¹åå ¶å¶å€æ¹æ³ |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU1109405A1 (ru) * | 1983-04-04 | 1984-08-23 | ÐеМОМгÑаЎÑкОй ÐÐœÑÑОÑÑÑ ÐОМПОМжеМеÑПв | ÐПМПглОÑОЎОлалкОлÑПÑÑаÑÑ Ð² каÑеÑÑве плаÑÑОÑОкаÑПÑПв ÑПÑПгÑаÑОÑеÑÐºÐžÑ Ð¶ÐµÐ»Ð°ÑОМПвÑÑ ÑÐŒÑлÑÑОПММÑÑ ÑлПев |
-
1986
- 1986-04-21 JP JP61091704A patent/JPS62249995A/ja active Granted
-
1987
- 1987-03-17 KR KR1019870002392A patent/KR940011186B1/ko not_active IP Right Cessation
- 1987-04-01 US US07/032,627 patent/US4845239A/en not_active Expired - Lifetime
- 1987-04-09 MY MYPI87000458A patent/MY101645A/en unknown
- 1987-04-14 ES ES87105556T patent/ES2015282B3/es not_active Expired - Lifetime
- 1987-04-14 DE DE8787105556T patent/DE3761140D1/de not_active Expired - Fee Related
- 1987-04-14 EP EP87105556A patent/EP0242781B1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE3761140D1 (de) | 1990-01-18 |
| MY101645A (en) | 1991-12-31 |
| US4845239A (en) | 1989-07-04 |
| ES2015282B3 (es) | 1990-08-16 |
| EP0242781B1 (en) | 1989-12-13 |
| KR870010065A (ko) | 1987-11-30 |
| EP0242781A3 (en) | 1988-04-20 |
| KR940011186B1 (ko) | 1994-11-26 |
| EP0242781A2 (en) | 1987-10-28 |
| JPS62249995A (ja) | 1987-10-30 |
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