KR940011524A - 폴리에테르 치환 이미드 화합물 및 그의 용도 - Google Patents
폴리에테르 치환 이미드 화합물 및 그의 용도 Download PDFInfo
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- KR940011524A KR940011524A KR1019930025440A KR930025440A KR940011524A KR 940011524 A KR940011524 A KR 940011524A KR 1019930025440 A KR1019930025440 A KR 1019930025440A KR 930025440 A KR930025440 A KR 930025440A KR 940011524 A KR940011524 A KR 940011524A
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- South Korea
- Prior art keywords
- carbon atoms
- residue
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- compound
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- -1 imide compounds Chemical class 0.000 title claims 7
- 239000004721 Polyphenylene oxide Substances 0.000 title abstract 2
- 229920000570 polyether Polymers 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract 8
- 239000004094 surface-active agent Substances 0.000 claims abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 17
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 5
- 125000004407 fluoroaryl group Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 150000003512 tertiary amines Chemical class 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- IPENDKRRWFURRE-UHFFFAOYSA-N fluoroimide Chemical compound C1=CC(F)=CC=C1N1C(=O)C(Cl)=C(Cl)C1=O IPENDKRRWFURRE-UHFFFAOYSA-N 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 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
-
- 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
- A61K8/69—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing fluorine
- A61K8/70—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing fluorine containing perfluoro groups, e.g. perfluoroethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/04—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/334—Polymers modified by chemical after-treatment with organic compounds containing sulfur
- C08G65/3344—Polymers modified by chemical after-treatment with organic compounds containing sulfur containing oxygen in addition to sulfur
- C08G65/3346—Polymers modified by chemical after-treatment with organic compounds containing sulfur containing oxygen in addition to sulfur having sulfur bound to carbon and oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/337—Polymers modified by chemical after-treatment with organic compounds containing other elements
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
- C09D5/082—Anti-corrosive paints characterised by the anti-corrosive pigment
- C09D5/086—Organic or non-macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/26—Sulfonamides
-
- 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
- C11D1/004—Surface-active compounds containing F
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Wood Science & Technology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Polyethers (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Detergent Compositions (AREA)
Abstract
본 발명은 신규한 이미드의 폴리에테르 치환 화합물 및 계면활성제로서의 그의 용도에 관한 것이다. 상기 화합물을 사용하여 계면활성제로 사용할 수 있고 저렴한 비용으로 간단하게 생산할 수 있는 플루오로기를 함유하는 폴리에테르 계면 활성제를 제공할 수 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (11)
- 하나 이상의 플루오로알킬 및 플루오로아릴기를 함유한 하기 일반식(1)의 화함물.상기 식 중, RF는 탄소수 1 내지 18의 직쇄 또는 분지쇄 플루오로아킬 잔기, 탄소수 6 내지 12의 플루오로알릴잔기, 탄소수 7 내지 18의 혼합 플루오로알킬아릴 잔기 또는 탄소수 2 내지 18의 플루오로화 모노 또는 폴리에테르이고, R은 (i) 탄소수 1 내지 24의 직쇄 또는 분지쇄 알킬 잔기, 탄소수 6 내지 12의 아릴 잔기 또는 탄소수 7 내지 24의 혼합 알킬아릴 잔기이며, 탄소 사슬에 산소, 질소 또는 황 원자가 개입될 수 있고, 또는 (ii) 추가로 상기 정의된 RF잔기이며, 두 RF잔기는 동일 또는 상이할 수 있고, Yl및 Y2는 각각또는기를 나타내고, m은 0 내지 6의 정수이고, n은 0 내지 6의 정수이고, PE는 5 내지 50의 에틸렌 옥사이드 단위 또는 5 내지 50의 프로필렌 옥사이드 단위 또는 5 내지 50의 에틸렌 옥사이드 및 프로필렌 옥사이드 단위의 혼합물로 이루어진 폴리에테르 사슬이고, RH는 수소 원자 또는 탄소수 1 내지 10의 직쇄 또는 분지쇄 알킬 잔기이다.
- 제1항에 있어서, RF가 탄소수 3 내지 10의 직쇄 또는 분지쇄 플루오로알킬 잔기 또는 탄소수 6 내지 12의 플루오로아릴 잔기인, 하나 이상의 플루오로알킬 및 플루오로아릴기를 함유한 이미드 화합물.
- 제1항에 있어서, RF가 탄소수 3 내지 10의 직쇄 또는 분지쇄 과플루오로알킬 잔기 또는 탄소수 5 내지 12의 과플루오로아릴 잔기인 하나 이상의 플루오로알킬 및 플루오로아릴기를 함유한 이미드 화합물.
- 제1항에 있어서, R이 탄소수 6 내지 14의 직쇄 또는 분지쇄 알킬 잔기, 탄소수 6 내지 12의 아릴 잔기, 탄소수 7 내지 14의 혼합 알킬아릴 잔기 또는 탄소수 3 내지 10의 직쇄 또는 분지쇄 과플루오로알킬 잔기인 이미드 화합물.
- 제1항에 있어서, Y1및 Y2가 각각기를 나타내는 이미드 화합물.
- 1항에 있어서, m 및 n이 0인 이미드 화합물.
- 제1항에 있어서, RH가 탄소수 2 내지 4의 직쇄 알킬 잔기인 이미드 화합물.
- 플루오로알킬 또는 플루오로아릴기를 함유하는 하기 일반식(Ⅱ)의 화합물을 3급 아민의 존재하에 하기 일반식(Ⅲ)의 아민과 반응시켜 하기 일반식(Ⅳ)의 화합물로 이루어진 반응 산물을 형성하고, 추가로 일반식(Ⅳ)의 화합물을 3급 아민의 존재하에 하기 일반식(Ⅴ)의 화합물과 반응시키는 것을 특징으로 하는 제1항에 따른, 하나 이상의 플루오로알킬 또는 플루오로아릴기를 함유하는 이미드 화합물의 제조방법.상기 식중 RF, m, Yl, PE, RH, R, n 및 Y2는 제1항에 정의한 바와 같고, A1는 할로겐 원자, 히드록시기, 알콕시기 및 카르복시기로 이루어진 군에서 선택된 반응성 이탈기를 나타내고, A2는 Al과 같은 의미이다.
- 제1항에 정의된 이미드 화합물 또는 그의 염을 계면 활성제로서 조성물에 가하는 것을 특징으로 하는 제1항에 따른 이미드 화합물 또는 그의 염의 사용방법.
- 일반식또는 일반식를 갖는 이미드 화합물.
- 제1항에 있어서, Yl및 Y2가 각각기를 나타내는 이미드 화합물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4240008A DE4240008A1 (de) | 1992-11-27 | 1992-11-27 | Polyethersubstituierte Imidverbindungen sowie deren Verwendung |
DEP4240008.2 | 1992-11-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR940011524A true KR940011524A (ko) | 1994-06-21 |
KR100281200B1 KR100281200B1 (ko) | 2001-02-01 |
Family
ID=6473858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930025440A KR100281200B1 (ko) | 1992-11-27 | 1993-11-26 | 폴리에테르 치환 이미드 화합물 및 그의 용도 |
Country Status (9)
Country | Link |
---|---|
US (1) | US5414120A (ko) |
EP (1) | EP0600294B1 (ko) |
JP (1) | JP3220582B2 (ko) |
KR (1) | KR100281200B1 (ko) |
CN (1) | CN1035328C (ko) |
CA (1) | CA2109853A1 (ko) |
DE (2) | DE4240008A1 (ko) |
ES (1) | ES2192189T3 (ko) |
TW (1) | TW279168B (ko) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100378667B1 (ko) * | 2000-08-31 | 2003-03-31 | 주식회사 참 존 | 가축분뇨등의 신속한 무취화 및 퇴비화 방법 및 그 조성물 |
US7037494B2 (en) * | 1997-10-14 | 2006-05-02 | The Board Of Regents Of The University Of Texas System | Formulations and methods for insect control |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3250777B2 (ja) * | 1995-02-13 | 2002-01-28 | セントラル硝子株式会社 | イミド類、その塩類およびそれらの製造法 |
US5874616A (en) * | 1995-03-06 | 1999-02-23 | Minnesota Mining And Manufacturing Company | Preparation of bis (fluoroalkylenesulfonyl) imides and (fluoroalkysulfony) (fluorosulfonyl) imides |
CN102489216B (zh) * | 2011-12-06 | 2014-01-22 | 华中师范大学 | 两性含氟离子型表面活性剂的制备方法与应用 |
GB201609437D0 (en) * | 2016-05-27 | 2016-07-13 | Sphere Fluidics Ltd | Surfactants |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1140188B (de) * | 1957-07-23 | 1962-11-29 | Minnesota Mining & Mfg | Verfahren zur Herstellung von N-Polyoxyalkylenperfluoralkansulfon-saeureamiden |
FR2088594A5 (ko) * | 1970-04-17 | 1972-01-07 | Ugine Kuhlmann | |
DE2238740C3 (de) * | 1972-08-05 | 1981-07-16 | Bayer Ag, 5090 Leverkusen | Perfluoralkylgruppenhaltige Polyäther und Verfahren zu deren Herstellung und deren Verwendung |
JPS5836037B2 (ja) * | 1980-06-27 | 1983-08-06 | ダイキン工業株式会社 | 含フツ素界面活性剤組成物 |
FR2527602A1 (fr) * | 1982-06-01 | 1983-12-02 | Anvar | Bis perhalogenoacyl- ou sulfonyl- imidures de metaux alcalins, leurs solutions solides avec des matieres plastiques et leur application a la constitution d'elements conducteurs pour des generateurs electrochimiques |
EP0211578A3 (en) * | 1985-07-24 | 1987-11-11 | Research Corporation | N-fluoro-n-perfluoromethyl sulfonamides |
US4697011A (en) * | 1985-07-24 | 1987-09-29 | Research Corporation | N-fluoro-N-perfluoromethyl sulfonamides |
JPH02180861A (ja) * | 1988-10-28 | 1990-07-13 | Minnesota Mining & Mfg Co <3M> | アルキルアリールオキシポリ(オキシアルキレン)アミンのスルホンアミド誘導体 |
-
1992
- 1992-11-27 DE DE4240008A patent/DE4240008A1/de not_active Withdrawn
-
1993
- 1993-10-28 TW TW082108977A patent/TW279168B/zh active
- 1993-11-12 US US08/150,722 patent/US5414120A/en not_active Expired - Fee Related
- 1993-11-15 EP EP93118470A patent/EP0600294B1/de not_active Expired - Lifetime
- 1993-11-15 ES ES93118470T patent/ES2192189T3/es not_active Expired - Lifetime
- 1993-11-15 DE DE59310331T patent/DE59310331D1/de not_active Expired - Fee Related
- 1993-11-19 JP JP31279793A patent/JP3220582B2/ja not_active Expired - Fee Related
- 1993-11-24 CA CA002109853A patent/CA2109853A1/en not_active Abandoned
- 1993-11-26 KR KR1019930025440A patent/KR100281200B1/ko not_active IP Right Cessation
- 1993-11-27 CN CN93120666A patent/CN1035328C/zh not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7037494B2 (en) * | 1997-10-14 | 2006-05-02 | The Board Of Regents Of The University Of Texas System | Formulations and methods for insect control |
KR100378667B1 (ko) * | 2000-08-31 | 2003-03-31 | 주식회사 참 존 | 가축분뇨등의 신속한 무취화 및 퇴비화 방법 및 그 조성물 |
Also Published As
Publication number | Publication date |
---|---|
JP3220582B2 (ja) | 2001-10-22 |
CN1035328C (zh) | 1997-07-02 |
CN1089960A (zh) | 1994-07-27 |
JPH07304865A (ja) | 1995-11-21 |
US5414120A (en) | 1995-05-09 |
EP0600294A2 (de) | 1994-06-08 |
EP0600294A3 (de) | 1995-04-19 |
KR100281200B1 (ko) | 2001-02-01 |
DE59310331D1 (de) | 2003-03-27 |
ES2192189T3 (es) | 2003-10-01 |
CA2109853A1 (en) | 1994-05-28 |
TW279168B (ko) | 1996-06-21 |
EP0600294B1 (de) | 2003-02-19 |
DE4240008A1 (de) | 1994-06-01 |
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