JP2002507594A - 有機ポリイソシアネート用の安定化剤 - Google Patents
有機ポリイソシアネート用の安定化剤Info
- Publication number
- JP2002507594A JP2002507594A JP2000537847A JP2000537847A JP2002507594A JP 2002507594 A JP2002507594 A JP 2002507594A JP 2000537847 A JP2000537847 A JP 2000537847A JP 2000537847 A JP2000537847 A JP 2000537847A JP 2002507594 A JP2002507594 A JP 2002507594A
- Authority
- JP
- Japan
- Prior art keywords
- polyisocyanates
- stabilizers
- organic polyisocyanates
- butyl
- organic
- 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.)
- Pending
Links
- 229920001228 polyisocyanate Polymers 0.000 title claims abstract description 24
- 239000005056 polyisocyanate Substances 0.000 title claims abstract description 24
- 239000003381 stabilizer Substances 0.000 title claims abstract description 13
- XCPFSALHURPPJE-UHFFFAOYSA-N (3,5-ditert-butyl-4-hydroxyphenyl) propanoate Chemical compound CCC(=O)OC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 XCPFSALHURPPJE-UHFFFAOYSA-N 0.000 claims abstract description 5
- -1 3,5-di-t-butyl-4-hydroxyphenylpropionic acid ester Chemical class 0.000 claims description 2
- OQEGTHPDXJEZSC-UHFFFAOYSA-N methyl 2-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound COC(=O)C(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 OQEGTHPDXJEZSC-UHFFFAOYSA-N 0.000 claims 1
- 239000004814 polyurethane Substances 0.000 description 5
- 229920002635 polyurethane Polymers 0.000 description 5
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 2
- ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 description 1
- VGHSXKTVMPXHNG-UHFFFAOYSA-N 1,3-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC(N=C=O)=C1 VGHSXKTVMPXHNG-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 241001550224 Apha Species 0.000 description 1
- 102100025989 Glyoxalase domain-containing protein 4 Human genes 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 101000857136 Homo sapiens Glyoxalase domain-containing protein 4 Proteins 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- YPGCWEMNNLXISK-UHFFFAOYSA-N hydratropic acid Chemical class OC(=O)C(C)C1=CC=CC=C1 YPGCWEMNNLXISK-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- DYUMLJSJISTVPV-UHFFFAOYSA-N phenyl propanoate Chemical compound CCC(=O)OC1=CC=CC=C1 DYUMLJSJISTVPV-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/18—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19813136A DE19813136C1 (de) | 1998-03-25 | 1998-03-25 | Verwendung von 3,5-Di-tert.-butyl-4-hydroxyphenylpropionsäureestern zur Stabilisierung von organischen Polyisocyanaten |
DE19813136.4 | 1998-03-25 | ||
PCT/EP1999/001689 WO1999048863A1 (fr) | 1998-03-25 | 1999-03-15 | Stabilisation de polyisocyanates organiques |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2002507594A true JP2002507594A (ja) | 2002-03-12 |
Family
ID=7862279
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000537847A Pending JP2002507594A (ja) | 1998-03-25 | 1999-03-15 | 有機ポリイソシアネート用の安定化剤 |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1082296A1 (fr) |
JP (1) | JP2002507594A (fr) |
KR (1) | KR20010042135A (fr) |
CN (1) | CN1294575A (fr) |
AU (1) | AU3145199A (fr) |
BR (1) | BR9909029A (fr) |
CA (1) | CA2325034A1 (fr) |
DE (1) | DE19813136C1 (fr) |
TW (1) | TW461898B (fr) |
WO (1) | WO1999048863A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018070540A1 (fr) * | 2016-10-14 | 2018-04-19 | 旭化成株式会社 | Composition d'isocyanate, procédé de production de composition d'isocyanate, et procédé de production de polymère d'isocyanate |
US11548975B2 (en) | 2016-10-14 | 2023-01-10 | Asahi Kasei Kabushiki Kaisha | Isocyanate composition and method for producing isocyanate polymer |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108003072B (zh) * | 2017-12-04 | 2020-08-28 | 万华化学(宁波)有限公司 | 一种异氰酸酯稳定剂及其制备方法 |
CN110872238B (zh) * | 2018-08-31 | 2022-07-12 | 万华化学集团股份有限公司 | 一种异氰酸酯稳定剂及其制备方法 |
CN111228245A (zh) * | 2020-02-27 | 2020-06-05 | 华侨大学 | 酚类化合物及其在药学上可接受的盐在制备抗乙型肝炎病毒的药物中的应用 |
TWI754527B (zh) * | 2021-01-27 | 2022-02-01 | 宏正自動科技股份有限公司 | 固定端子 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1197437A (en) * | 1966-09-23 | 1970-07-01 | Ici Ltd | Stabilisation of Isocyanates |
US3715301A (en) * | 1971-06-30 | 1973-02-06 | Texaco Inc | Multi-hydrotorting of coal |
US4064157A (en) * | 1976-03-29 | 1977-12-20 | The Dow Chemical Company | Stabilization of polyisocyanates against discoloration |
DE59101819D1 (de) * | 1990-03-07 | 1994-07-14 | Bayer Ag | Stabilisierung von organischen Polyisocyanaten. |
CA2302707A1 (fr) * | 1997-09-30 | 1999-04-08 | Rosemarie A. Boccuzzi | Polyol de polyether stabilise et mousse de polyurethanne obtenue a partir de ce polyol |
-
1998
- 1998-03-25 DE DE19813136A patent/DE19813136C1/de not_active Expired - Fee Related
-
1999
- 1999-03-15 KR KR1020007010539A patent/KR20010042135A/ko not_active Application Discontinuation
- 1999-03-15 CN CN99804416A patent/CN1294575A/zh active Pending
- 1999-03-15 AU AU31451/99A patent/AU3145199A/en not_active Abandoned
- 1999-03-15 CA CA002325034A patent/CA2325034A1/fr not_active Abandoned
- 1999-03-15 WO PCT/EP1999/001689 patent/WO1999048863A1/fr not_active Application Discontinuation
- 1999-03-15 JP JP2000537847A patent/JP2002507594A/ja active Pending
- 1999-03-15 BR BR9909029-5A patent/BR9909029A/pt not_active Application Discontinuation
- 1999-03-15 EP EP99913256A patent/EP1082296A1/fr not_active Withdrawn
- 1999-03-18 TW TW088104181A patent/TW461898B/zh active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018070540A1 (fr) * | 2016-10-14 | 2018-04-19 | 旭化成株式会社 | Composition d'isocyanate, procédé de production de composition d'isocyanate, et procédé de production de polymère d'isocyanate |
JPWO2018070540A1 (ja) * | 2016-10-14 | 2019-04-25 | 旭化成株式会社 | イソシアネート組成物、イソシアネート組成物の製造方法、及びイソシアネート重合体の製造方法 |
US11118001B2 (en) | 2016-10-14 | 2021-09-14 | Asahi Kasei Kabushiki Kaisha | Isocyanate composition, method for producing isocyanate composition, and method for producing isocyanate polymer |
US11548975B2 (en) | 2016-10-14 | 2023-01-10 | Asahi Kasei Kabushiki Kaisha | Isocyanate composition and method for producing isocyanate polymer |
Also Published As
Publication number | Publication date |
---|---|
TW461898B (en) | 2001-11-01 |
KR20010042135A (ko) | 2001-05-25 |
EP1082296A1 (fr) | 2001-03-14 |
BR9909029A (pt) | 2000-12-05 |
CN1294575A (zh) | 2001-05-09 |
WO1999048863A1 (fr) | 1999-09-30 |
AU3145199A (en) | 1999-10-18 |
DE19813136C1 (de) | 1999-07-15 |
CA2325034A1 (fr) | 1999-09-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100307257B1 (ko) | 1,3-비스(1-메틸-1-이소시아네이토에틸)벤젠을기재로하는카르보디이미드및/또는올리고머폴리카르보디이미드,이들의제조방법및가수분해안정화제로서의이들의사용방법 | |
JP5632067B2 (ja) | ウレトンイミン変性イソシアネート組成物の製造方法 | |
EP1846367A1 (fr) | Diisocyanates aliphatiques, cycloaliphatiques ou (cyclo)aliphatiques stables au stockage | |
KR100191882B1 (ko) | 유기 폴리이소시아네이트의 안정화 방법 | |
CN109641834B (zh) | 用于制备具有碳二亚胺-和/或脲酮亚胺基团的有机异氰酸酯的方法 | |
JP2002507594A (ja) | 有機ポリイソシアネート用の安定化剤 | |
CA1317965C (fr) | Polyisocyanates stabilises | |
US5359129A (en) | Method for preventing coloration of diphenylmethane diisocyanate compound | |
JPS59120617A (ja) | ポリウレタン予備重合体硬化用組成物 | |
EP0032011B1 (fr) | Mélanges d'isocyanates modifiés | |
US5185384A (en) | Method for reducing hydrolyzable chloride in toluene diisocyanate | |
JPH0579691B2 (fr) | ||
US4318861A (en) | Stabilized diphenylmethane diisocyanate-polymethylene polyphenyl isocyanate compositions | |
US5476892A (en) | Process for conditioning and stabilizing polyols | |
MXPA00009319A (en) | Stabilisation of organic polyisocyanates | |
US4320069A (en) | Oxazoline stabilized diphenylmethane diisocyanate-polymethylene polyphenyl isocyanate compositions | |
JP2000290243A5 (fr) | ||
US4332741A (en) | Dichloroparabanic acid stabilized diphenylmethane diisocyanate-polymethylene polyphenyl isocyanate compositions | |
JPS5958022A (ja) | 安定化したポリイソシアネ−ト組成物の製造方法 | |
JPH0920744A (ja) | イソシアナート化合物の着色防止方法 | |
JP3228801B2 (ja) | イソシアヌレート基含有ポリイソシアネートの製法 | |
WO2023083877A1 (fr) | Procédé de production de carbodiimides polymères aromatiques | |
JPS6023695B2 (ja) | 部分ウレタン化脂環族カルボジイミドの製造方法 | |
JPS5993038A (ja) | ポリイソシアネ−ト組成物 | |
DE4041516A1 (de) | Stabilisierung von organischen polyisocyanaten |