KR930017855A - 안정화제로 유용한 히드록시페닐알칸올의 카르복시산 에스테르 - Google Patents
안정화제로 유용한 히드록시페닐알칸올의 카르복시산 에스테르 Download PDFInfo
- Publication number
- KR930017855A KR930017855A KR1019930002551A KR930002551A KR930017855A KR 930017855 A KR930017855 A KR 930017855A KR 1019930002551 A KR1019930002551 A KR 1019930002551A KR 930002551 A KR930002551 A KR 930002551A KR 930017855 A KR930017855 A KR 930017855A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- unsubstituted
- substituted
- alkenyl
- formula
- 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.)
- Withdrawn
Links
- 150000001733 carboxylic acid esters Chemical class 0.000 title 1
- 239000003381 stabilizer Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract 29
- 150000001875 compounds Chemical class 0.000 claims abstract 21
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract 15
- 230000003647 oxidation Effects 0.000 claims abstract 6
- 238000007254 oxidation reaction Methods 0.000 claims abstract 6
- 239000011368 organic material Substances 0.000 claims abstract 5
- 230000000087 stabilizing effect Effects 0.000 claims abstract 4
- 238000000354 decomposition reaction Methods 0.000 claims abstract 3
- -1 heterocyclic radical Chemical class 0.000 claims 15
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 12
- 125000002947 alkylene group Chemical group 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 7
- 125000002993 cycloalkylene group Chemical group 0.000 claims 6
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 4
- 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 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 239000007983 Tris buffer Substances 0.000 claims 3
- 125000004450 alkenylene group Chemical group 0.000 claims 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 3
- 125000005724 cycloalkenylene group Chemical group 0.000 claims 3
- 125000003884 phenylalkyl group Chemical group 0.000 claims 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims 2
- 235000010290 biphenyl Nutrition 0.000 claims 2
- 239000004305 biphenyl Substances 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 230000015556 catabolic process Effects 0.000 claims 2
- 238000006731 degradation reaction Methods 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000001326 naphthylalkyl group Chemical group 0.000 claims 2
- 125000004957 naphthylene group Chemical group 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 229930192474 thiophene Natural products 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims 1
- 239000003963 antioxidant agent Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- GYTKHIWTONFGKP-UHFFFAOYSA-N bis[6-(3,5-ditert-butyl-4-hydroxyphenyl)hexyl] benzene-1,3-dicarboxylate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCCCCCOC(=O)C=2C=C(C=CC=2)C(=O)OCCCCCCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 GYTKHIWTONFGKP-UHFFFAOYSA-N 0.000 claims 1
- SMBCSJBYDSGLKV-UHFFFAOYSA-N bis[6-(3-tert-butyl-4-hydroxy-5-methylphenyl)hexyl] benzene-1,3-dicarboxylate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCCCCCOC(=O)C=2C=C(C=CC=2)C(=O)OCCCCCCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 SMBCSJBYDSGLKV-UHFFFAOYSA-N 0.000 claims 1
- DJJPODJJYQUWEP-UHFFFAOYSA-N bis[6-(3-tert-butyl-4-hydroxy-5-methylphenyl)hexyl] octanedioate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCCCCCOC(=O)CCCCCCC(=O)OCCCCCCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 DJJPODJJYQUWEP-UHFFFAOYSA-N 0.000 claims 1
- 238000002144 chemical decomposition reaction Methods 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229920000098 polyolefin Polymers 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 229920005613 synthetic organic polymer Polymers 0.000 claims 1
- 125000005591 trimellitate group Chemical group 0.000 claims 1
- BNHUYUGAGHERJD-UHFFFAOYSA-N tris[6-(3-tert-butyl-4-hydroxy-5-methylphenyl)hexyl] benzene-1,3,5-tricarboxylate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCCCCCOC(=O)C=2C=C(C=C(C=2)C(=O)OCCCCCCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)C(=O)OCCCCCCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 BNHUYUGAGHERJD-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/11—Alkylated hydroxy benzenes containing also acyclically bound hydroxy groups, e.g. saligenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/612—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/17—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings containing other rings in addition to the six-membered aromatic rings, e.g. cyclohexylphenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/007—Esters of unsaturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH54792 | 1992-02-24 | ||
| CH92-1/547 | 1992-02-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR930017855A true KR930017855A (ko) | 1993-09-20 |
Family
ID=4189515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019930002551A Withdrawn KR930017855A (ko) | 1992-02-24 | 1993-02-22 | 안정화제로 유용한 히드록시페닐알칸올의 카르복시산 에스테르 |
Country Status (19)
| Country | Link |
|---|---|
| JP (1) | JPH0641009A (en:Method) |
| KR (1) | KR930017855A (en:Method) |
| CN (1) | CN1077448A (en:Method) |
| AT (1) | ATA32793A (en:Method) |
| BE (1) | BE1006547A5 (en:Method) |
| BR (1) | BR9300632A (en:Method) |
| CA (1) | CA2090082A1 (en:Method) |
| CZ (1) | CZ25593A3 (en:Method) |
| DE (1) | DE4305422A1 (en:Method) |
| ES (1) | ES2060540B1 (en:Method) |
| FR (1) | FR2687667B1 (en:Method) |
| GB (1) | GB2264708B (en:Method) |
| IT (1) | IT1263954B (en:Method) |
| MX (1) | MX9300987A (en:Method) |
| NL (1) | NL9300336A (en:Method) |
| SE (1) | SE9300579L (en:Method) |
| SK (1) | SK11293A3 (en:Method) |
| TW (1) | TW225522B (en:Method) |
| ZA (1) | ZA931249B (en:Method) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5012090B2 (ja) * | 2007-03-02 | 2012-08-29 | 住友化学株式会社 | ３−（ｐ−ヒドロキシフェニル）プロパノール類の製造方法 |
| DE102009028862A1 (de) * | 2008-12-22 | 2010-07-01 | Evonik Degussa Gmbh | Monomerarme 1 : 1 Monoaddukte aus reaktiven olefinischen Verbindungen und Diisocyanaten unter Verwendung einbaubarer Inhibitoren |
| US8901362B2 (en) * | 2012-02-02 | 2014-12-02 | General Electric Company | Methods and compositions for styrene inhibition via in situ generation of quinone methides |
| EP3184567A1 (de) | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylatterminierte urethanpolybutadiene aus monomerarmen 1:1 monoaddukten aus reaktiven olfinischen verbindungen und diisocyanaten und hydroxyterminierten polybutadienen |
| EP3184568A1 (en) | 2015-12-21 | 2017-06-28 | Evonik Degussa GmbH | Acrylate-terminated urethane polybutadienes from low-monomer 1:1 monoadductes from reactive olefinic compounds and diisocyanates and hydroxy-terminated polybutadienes for liquid optically clear adhesives (locas) |
| CN107382728B (zh) * | 2017-08-02 | 2020-01-21 | 大理大学 | 2-(3,4-二羟基苯基)乙醇丁二酸二酯及其提取方法和应用 |
| CN109337003A (zh) * | 2018-09-19 | 2019-02-15 | 长春永固科技有限公司 | 一种可光降解的高分子材料及其制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4260832A (en) * | 1979-10-29 | 1981-04-07 | The Goodyear Tire & Rubber Company | Alkylation of 2,6-di-tert-alkylphenols with alkanediols |
| CA1338012C (en) * | 1987-04-27 | 1996-01-30 | John Michael Mccall | Pharmaceutically active amines |
| DE3717448A1 (de) * | 1987-05-23 | 1988-12-08 | Huels Chemische Werke Ag | Stabilisatormischungen und damit stabilisierte formmassen auf der basis von polymerisaten des vinylchlorids |
-
1993
- 1993-02-08 TW TW082100835A patent/TW225522B/zh active
- 1993-02-18 BE BE9300154A patent/BE1006547A5/fr not_active IP Right Cessation
- 1993-02-19 BR BR9300632A patent/BR9300632A/pt not_active Application Discontinuation
- 1993-02-22 CA CA002090082A patent/CA2090082A1/en not_active Abandoned
- 1993-02-22 DE DE4305422A patent/DE4305422A1/de not_active Withdrawn
- 1993-02-22 GB GB9303500A patent/GB2264708B/en not_active Expired - Fee Related
- 1993-02-22 SK SK11293A patent/SK11293A3/sk unknown
- 1993-02-22 IT ITMI930337A patent/IT1263954B/it active IP Right Grant
- 1993-02-22 SE SE9300579A patent/SE9300579L/ not_active Application Discontinuation
- 1993-02-22 KR KR1019930002551A patent/KR930017855A/ko not_active Withdrawn
- 1993-02-22 AT AT0032793A patent/ATA32793A/de not_active Application Discontinuation
- 1993-02-22 CZ CZ93255A patent/CZ25593A3/cs unknown
- 1993-02-23 CN CN93101955A patent/CN1077448A/zh active Pending
- 1993-02-23 NL NL9300336A patent/NL9300336A/nl active Search and Examination
- 1993-02-23 ZA ZA931249A patent/ZA931249B/xx unknown
- 1993-02-23 FR FR9302037A patent/FR2687667B1/fr not_active Expired - Fee Related
- 1993-02-23 ES ES09300354A patent/ES2060540B1/es not_active Expired - Fee Related
- 1993-02-24 JP JP5059686A patent/JPH0641009A/ja active Pending
- 1993-02-24 MX MX9300987A patent/MX9300987A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| SE9300579D0 (sv) | 1993-02-22 |
| JPH0641009A (ja) | 1994-02-15 |
| GB2264708B (en) | 1995-09-27 |
| NL9300336A (nl) | 1993-09-16 |
| FR2687667B1 (fr) | 1996-03-22 |
| GB2264708A (en) | 1993-09-08 |
| SK11293A3 (en) | 1993-10-06 |
| ITMI930337A0 (it) | 1993-02-22 |
| CN1077448A (zh) | 1993-10-20 |
| TW225522B (en:Method) | 1994-06-21 |
| FR2687667A1 (fr) | 1993-08-27 |
| ITMI930337A1 (it) | 1994-08-22 |
| ES2060540B1 (es) | 1996-03-16 |
| ATA32793A (de) | 1997-11-15 |
| CA2090082A1 (en) | 1993-08-25 |
| MX9300987A (es) | 1993-09-01 |
| IT1263954B (it) | 1996-09-05 |
| BR9300632A (pt) | 1993-08-31 |
| CZ25593A3 (en) | 1993-12-15 |
| ES2060540A1 (es) | 1994-11-16 |
| BE1006547A5 (fr) | 1994-10-11 |
| SE9300579L (sv) | 1993-08-25 |
| DE4305422A1 (en:Method) | 1993-08-26 |
| GB9303500D0 (en) | 1993-04-07 |
| ZA931249B (en) | 1993-08-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19930222 |
|
| PG1501 | Laying open of application | ||
| N231 | Notification of change of applicant | ||
| PN2301 | Change of applicant |
Patent event date: 19970224 Comment text: Notification of Change of Applicant Patent event code: PN23011R01D |
|
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |