KR930016432A - 시클로알킬리덴 비스페놀 포스파이트 및 그의 제조방법 - Google Patents
시클로알킬리덴 비스페놀 포스파이트 및 그의 제조방법 Download PDFInfo
- Publication number
- KR930016432A KR930016432A KR1019930000853A KR930000853A KR930016432A KR 930016432 A KR930016432 A KR 930016432A KR 1019930000853 A KR1019930000853 A KR 1019930000853A KR 930000853 A KR930000853 A KR 930000853A KR 930016432 A KR930016432 A KR 930016432A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- hydrogen
- composition
- formula
- alkyl
- Prior art date
Links
- 229930185605 Bisphenol Natural products 0.000 title 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 title 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 title 1
- 238000002360 preparation method Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 15
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 14
- 239000001257 hydrogen Substances 0.000 claims abstract 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 10
- 150000002431 hydrogen Chemical class 0.000 claims abstract 4
- 239000011368 organic material Substances 0.000 claims abstract 4
- 230000003647 oxidation Effects 0.000 claims abstract 3
- 238000007254 oxidation reaction Methods 0.000 claims abstract 3
- 239000003381 stabilizer Substances 0.000 claims abstract 3
- 230000015556 catabolic process Effects 0.000 claims abstract 2
- 238000006731 degradation reaction Methods 0.000 claims abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 238000000034 method Methods 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 239000004698 Polyethylene Substances 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- DQTRYXANLKJLPK-UHFFFAOYSA-N chlorophosphonous acid Chemical compound OP(O)Cl DQTRYXANLKJLPK-UHFFFAOYSA-N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- 239000004611 light stabiliser Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- -1 polyethylene Polymers 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 claims 1
- 239000004800 polyvinyl chloride Substances 0.000 claims 1
- 229920000915 polyvinyl chloride Polymers 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 229920001059 synthetic polymer Polymers 0.000 claims 1
- 229920001169 thermoplastic Polymers 0.000 claims 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
- C07F9/547—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
- C07F9/65748—Esters of oxyacids of phosphorus the cyclic phosphorus atom belonging to more than one ring system
-
- 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
- C07F9/65746—Esters of oxyacids of phosphorus the molecule containing more than one cyclic phosphorus atom
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Abstract
Description
Claims (18)
- 하기 일반식(Ⅰ)의 화합물,상기 식에서, n은 0,1 또는 2이고 R 및 R1은 독립적으로 C1-C4알킬 또는 함께 결합되어 형성된 2,3-디히드로펜타메틸렌 라디칼이며, R2및 R3는 독립적으로 수소 또는 C5-C4알킬 또는 C1-C6시클로알킬 그리고, R4, R5및 R7는 n이 1인 경우, 독립적으로 수소, 또는 C1-C4알킬이며, n이 0 및 2인 경우 수소이다.
- 제1항에 있어서 n이 1 또는 2인 화합물.
- 제1항에 있어서 R2및 R3가 독립적으로 수소 C1-C4알킬 또는 시클로헥실인 화합물.
- 제1항에 있어서 n이 1인 화합물.
- 제1항에 있어서 n이 1이며 R4가 수소이고, R5, R6및 R7이 독립적으로 수소 또는 메틸인 화합물.
- 제1항에 있어서 R2및 R3가 독립적으로 수소, 메탈, 부틸 또는 시클로헥실인 화합물.
- 제1항에 있어서, R2및 R3가 독립적으로 수소, 메틸 또는 3차 부틸인 화합물.
- 제1항에 있어서, R5, R6및 R7이 수소이며 R4가 수소 또는 3차부틸인 화합물.
- 제1항에 있어서, R4, R5, R6및 R7이 수소인 화합물.
- 제1항에 있어서, R 및 R1이 독립적으로 메틸은 부틸이거나, 함께 결합되어 형성된 2,3-디히드로펜타메틸렌 라디칼인 화합물.
- 산화, 열 및 광-유발 분해에 민감한 유기 물질(a) 및 제1항에 따른 일반식(Ⅰ)의 화합물 1개 이상(b)을 포함하는 조성물.
- 제11항에 있어서, 성분(a)가 천연, 반-합성 또는 합성 중합체인 조성물.
- 제11항에 있어서, 성분(a)가 열가소성 중합체인 조성물.
- 제11항에 있어서, 성분(a)가 폴리올레핀 또는 폴리비닐 클로라이드인 조성물.
- 제11항에 있어서, 성분(a)가 폴리에틸렌 또는 포릴프로필렌인 조성물.
- 제11항에 있어서, 성분(a) 및 (b)이외에도 산화 방지제, 광안정화제 또는 공정 안정화제를 포함하는 조성물.
- 안정화제로서 일반식(Ⅰ)화합물 1개 이상을 유기 물질에 혼입 또는 도포하여 산화, 열 및 광유발 분해로부터 유기 물질을 보호하는 방법.
- 하기 일반(Ⅱ)의 화합물을 하기 일반식(Ⅲa)의 시클릭 클로로포스파이트와 반응시켜 일반식(Ⅰ)의 화합물을 제조하는 방법.상기 식에서, 치환체 R, R1, R2, R3, R4, R5, R6, R7과 n은 제1항에서 정의한 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH92-0/149 | 1992-01-21 | ||
CH14992 | 1992-01-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR930016432A true KR930016432A (ko) | 1993-08-26 |
Family
ID=4180367
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930000853A KR930016432A (ko) | 1992-01-21 | 1993-01-21 | 시클로알킬리덴 비스페놀 포스파이트 및 그의 제조방법 |
Country Status (16)
Country | Link |
---|---|
US (1) | US5280057A (ko) |
EP (1) | EP0553059B1 (ko) |
JP (1) | JPH0625271A (ko) |
KR (1) | KR930016432A (ko) |
CN (1) | CN1075968A (ko) |
AT (1) | ATE143966T1 (ko) |
AU (1) | AU656255B2 (ko) |
BR (1) | BR9300218A (ko) |
CA (1) | CA2087582A1 (ko) |
CZ (1) | CZ5093A3 (ko) |
DE (1) | DE59304064D1 (ko) |
ES (1) | ES2095025T3 (ko) |
MX (1) | MX9207621A (ko) |
SK (1) | SK1393A3 (ko) |
TW (1) | TW260688B (ko) |
ZA (1) | ZA93380B (ko) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6140432A (en) * | 1995-07-13 | 2000-10-31 | Exxon Chemical Patents Inc. | Polymerization catalyst systems, their production and use |
US6124230A (en) * | 1995-07-13 | 2000-09-26 | Exxon Chemical Patents, Inc. | Polymerization catalyst systems, their production and use |
TW338046B (en) * | 1995-06-29 | 1998-08-11 | Ciba Sc Holding Ag | Process for the preparation of stabilized olefin polymers |
US5594053A (en) * | 1996-01-22 | 1997-01-14 | General Electric Company | Aromatic cyclic bisphosphite esters and polymeric compositions thereof |
US8142864B2 (en) * | 2007-01-25 | 2012-03-27 | Konica Minolta Opto, Inc. | Cellulose ester pellets, cellulose ester film, manufacturing method of cellulose ester film, polarizing plate, and liquid crystal display |
US8466096B2 (en) * | 2007-04-26 | 2013-06-18 | Afton Chemical Corporation | 1,3,2-dioxaphosphorinane, 2-sulfide derivatives for use as anti-wear additives in lubricant compositions |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2883365A (en) * | 1955-03-01 | 1959-04-21 | Goodrich Co B F | Sulfur vulcanizable rubber and 1,1-bis(4-hydroxy phenyl) cycloalkane |
US2894004A (en) * | 1956-08-13 | 1959-07-07 | Dow Chemical Co | Bisphenols |
US3039993A (en) * | 1960-05-10 | 1962-06-19 | Weston Chemical Corp | Polyethylene stabilizers |
DE1237312B (de) * | 1961-06-27 | 1967-03-23 | Pure Chem Ltd | Formmassen aus Polymerisaten von Olefinen |
FR1384809A (fr) * | 1963-11-28 | 1965-01-08 | Kuhlmann Ets | Nouveaux esters phosphoreux, procédé pour leur fabrication et applications desdits esters |
US3467733A (en) * | 1965-11-26 | 1969-09-16 | Hooker Chemical Corp | Cyclic esters of phosphorus and a process for the preparation thereof |
US3441633A (en) * | 1965-12-03 | 1969-04-29 | Weston Chemical Corp | Cyclic phosphites |
US3491157A (en) * | 1968-01-11 | 1970-01-20 | Dow Chemical Co | Cycloalkylidenebis(cycloalkylphenols) |
US3655832A (en) * | 1969-02-18 | 1972-04-11 | Argus Chem | Polycarbocyclic phenolic phosphites |
US3856728A (en) * | 1971-04-26 | 1974-12-24 | Argus Chem | Acrylonitrile-butadiene-styrene polymers having improved resistance to discoloration |
US4206111A (en) * | 1977-05-06 | 1980-06-03 | Borg-Warner Corporation | Stabilized polyolefins |
GB2042562B (en) * | 1979-02-05 | 1983-05-11 | Sandoz Ltd | Stabilising polymers |
US4312803A (en) * | 1979-03-16 | 1982-01-26 | General Electric Company | Thermally stable polycarbonate compositions |
JPS5692934A (en) * | 1979-12-26 | 1981-07-28 | Adeka Argus Chem Co Ltd | Synthetic resin composition |
US4463112A (en) * | 1980-02-13 | 1984-07-31 | Leistner William E | Phenylethylidene-substituted phenyl polyphosphites |
-
1992
- 1992-12-30 MX MX9207621A patent/MX9207621A/es unknown
-
1993
- 1993-01-12 DE DE59304064T patent/DE59304064D1/de not_active Expired - Fee Related
- 1993-01-12 EP EP93810013A patent/EP0553059B1/de not_active Expired - Lifetime
- 1993-01-12 ES ES93810013T patent/ES2095025T3/es not_active Expired - Lifetime
- 1993-01-12 AT AT93810013T patent/ATE143966T1/de not_active IP Right Cessation
- 1993-01-13 TW TW082100164A patent/TW260688B/zh active
- 1993-01-13 US US08/004,147 patent/US5280057A/en not_active Expired - Fee Related
- 1993-01-15 AU AU31841/93A patent/AU656255B2/en not_active Ceased
- 1993-01-18 SK SK1393A patent/SK1393A3/sk unknown
- 1993-01-19 BR BR9300218A patent/BR9300218A/pt not_active Application Discontinuation
- 1993-01-19 CA CA002087582A patent/CA2087582A1/en not_active Abandoned
- 1993-01-20 CZ CZ9350A patent/CZ5093A3/cs unknown
- 1993-01-20 ZA ZA93380A patent/ZA93380B/xx unknown
- 1993-01-20 CN CN93100816A patent/CN1075968A/zh active Pending
- 1993-01-21 KR KR1019930000853A patent/KR930016432A/ko not_active Application Discontinuation
- 1993-01-21 JP JP5026090A patent/JPH0625271A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
ATE143966T1 (de) | 1996-10-15 |
CN1075968A (zh) | 1993-09-08 |
AU656255B2 (en) | 1995-01-27 |
SK1393A3 (en) | 1993-09-09 |
DE59304064D1 (de) | 1996-11-14 |
US5280057A (en) | 1994-01-18 |
ZA93380B (en) | 1993-07-21 |
TW260688B (ko) | 1995-10-21 |
EP0553059B1 (de) | 1996-10-09 |
ES2095025T3 (es) | 1997-02-01 |
EP0553059A1 (de) | 1993-07-28 |
CA2087582A1 (en) | 1993-07-22 |
AU3184193A (en) | 1993-07-22 |
MX9207621A (es) | 1993-07-01 |
BR9300218A (pt) | 1993-07-27 |
JPH0625271A (ja) | 1994-02-01 |
CZ5093A3 (en) | 1993-10-13 |
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