GB1143754A - - Google Patents
Info
- Publication number
- GB1143754A GB1143754A GB1143754DA GB1143754A GB 1143754 A GB1143754 A GB 1143754A GB 1143754D A GB1143754D A GB 1143754DA GB 1143754 A GB1143754 A GB 1143754A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepolymer
- ethylene imine
- reacted
- imine
- glycol ether
- 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.)
- Active
Links
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 abstract 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 6
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 6
- -1 polybutylene Polymers 0.000 abstract 5
- 229920001748 polybutylene Polymers 0.000 abstract 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 4
- 150000001412 amines Chemical class 0.000 abstract 4
- 229910021529 ammonia Inorganic materials 0.000 abstract 3
- 239000005057 Hexamethylene diisocyanate Substances 0.000 abstract 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 abstract 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 abstract 2
- 239000005056 polyisocyanate Substances 0.000 abstract 2
- 229920001228 polyisocyanate Polymers 0.000 abstract 2
- 229920005862 polyol Polymers 0.000 abstract 2
- 150000003077 polyols Chemical class 0.000 abstract 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 2
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 abstract 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 abstract 1
- KNIUHBNRWZGIQQ-UHFFFAOYSA-N 7-diethoxyphosphinothioyloxy-4-methylchromen-2-one Chemical compound CC1=CC(=O)OC2=CC(OP(=S)(OCC)OCC)=CC=C21 KNIUHBNRWZGIQQ-UHFFFAOYSA-N 0.000 abstract 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229930182556 Polyacetal Natural products 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002429 hydrazines Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000002466 imines Chemical class 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- 150000002513 isocyanates Chemical class 0.000 abstract 1
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920006324 polyoxymethylene Polymers 0.000 abstract 1
- 229920001451 polypropylene glycol Polymers 0.000 abstract 1
- 150000004992 toluidines Chemical class 0.000 abstract 1
Classifications
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/83—Chemically modified polymers
- C08G18/833—Chemically modified polymers by nitrogen containing compounds
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S528/903—Polymerizing or processing an isocyanate under substantially anhydrous conditions
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF47714A DE1301115B (de) | 1965-11-19 | 1965-11-19 | Verfahren zur Herstellung von definierten, hoehermolekularen Aminen |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1143754A true GB1143754A (en, 2012) |
Family
ID=7101791
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1143754D Active GB1143754A (en, 2012) | 1965-11-19 |
Country Status (4)
Country | Link |
---|---|
US (1) | US3471449A (en, 2012) |
DE (1) | DE1301115B (en, 2012) |
FR (1) | FR1508209A (en, 2012) |
GB (1) | GB1143754A (en, 2012) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4338242A (en) * | 1980-09-19 | 1982-07-06 | The Dow Chemical Company | Urethane modified polymers having hydroxyl groups |
US4383091A (en) * | 1980-09-19 | 1983-05-10 | The Dow Chemical Company | Urethane modified polymers having hydroxyl groups |
EP0112824A4 (en) * | 1982-07-02 | 1984-11-05 | Dow Chemical Co | VINYL ESTER MODIFIED BY URETHAN WITH SECONDARY HYDROXYL GROUPS. |
US5055544A (en) * | 1987-09-21 | 1991-10-08 | The Dow Chemical Company | Amino-functional polyesters containing urea, biuret, thiourea, dithiobiuret, thioamide, and/or amide moieties in their backbone and urethane/urea prepolymers and polymers made therefrom |
US4916201A (en) * | 1987-09-21 | 1990-04-10 | The Dow Chemical Company | Amino-functional polyethers containing urea, biuret, thiourea, dithiobiuret, thioamide, and/or amide moieties in their backbone and urethane/urea prepolymers and polymers made therefrom |
US5115070A (en) * | 1990-03-09 | 1992-05-19 | The Dow Chemical Company | Polyalkyleneoxy polyahis containing hydrogen bonding moieties in their backbone and hydroxyalkyl carbamate end groups and a process for their preparation |
DE19919482C2 (de) * | 1999-04-29 | 2001-04-26 | Byk Chemie Gmbh | Verfahren zur Herstellung eines Thixotropie-Mittels und dessen Verwendung |
JP6423000B2 (ja) | 2014-04-15 | 2018-11-14 | ビイク−ヒエミー ゲゼルシャフト ミツト ベシユレンクテル ハフツングBYK−Chemie GmbH | レオロジー調整のための組成物 |
CN112079982B (zh) * | 2020-09-21 | 2022-04-15 | 浙江华峰合成树脂有限公司 | 一种超柔仿蛋白质耐水解聚氨酯树脂及制备 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA612937A (en) * | 1961-01-17 | R. Little Julian | Rubber chemicals | |
US2888439A (en) * | 1957-08-16 | 1959-05-26 | Du Pont | Polyurethane diamines |
DE1112286B (de) * | 1959-06-19 | 1961-08-03 | Bayer Ag | Verfahren zur Herstellung vernetzter Urethan- und Harnstoffgruppen aufweisender Kunststoffe |
US3054757A (en) * | 1960-02-08 | 1962-09-18 | Mobay Chemical Corp | Polyurethane production with imines as catalysts |
NL286137A (en, 2012) * | 1961-08-16 | |||
US3146219A (en) * | 1962-04-20 | 1964-08-25 | Air Prod & Chem | Catalyst composition and method of using same |
US3361844A (en) * | 1964-12-14 | 1968-01-02 | Du Pont | Polyurethane/polyurea product and process for preparing same |
-
0
- GB GB1143754D patent/GB1143754A/en active Active
-
1965
- 1965-11-19 DE DEF47714A patent/DE1301115B/de active Pending
-
1966
- 1966-11-15 FR FR83690A patent/FR1508209A/fr not_active Expired
- 1966-11-17 US US594991A patent/US3471449A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US3471449A (en) | 1969-10-07 |
DE1301115B (de) | 1969-08-14 |
FR1508209A (fr) | 1968-01-05 |
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