GB1381011A - Methylolglycidyl ethers of polyhydric phenol ethers a process for their manufacture and cursable mixtures containing them - Google Patents
Methylolglycidyl ethers of polyhydric phenol ethers a process for their manufacture and cursable mixtures containing themInfo
- Publication number
- GB1381011A GB1381011A GB2220572A GB2220572A GB1381011A GB 1381011 A GB1381011 A GB 1381011A GB 2220572 A GB2220572 A GB 2220572A GB 2220572 A GB2220572 A GB 2220572A GB 1381011 A GB1381011 A GB 1381011A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethers
- alkyl
- groups
- optionally substituted
- glycidyl
- 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.)
- Expired
Links
- SORVTOKVRKOQCP-UHFFFAOYSA-N oxiran-2-ylmethoxymethanol Chemical class OCOCC1CO1 SORVTOKVRKOQCP-UHFFFAOYSA-N 0.000 title abstract 2
- 150000008379 phenol ethers Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- -1 C3B Methylol glycidyl ethers Chemical class 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004450 alkenylene group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 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 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical group C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 abstract 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 238000010533 azeotropic distillation Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/08—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols from phenol-aldehyde condensates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- C08G59/3218—Carbocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Compounds (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH728271 | 1971-05-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1381011A true GB1381011A (en) | 1975-01-22 |
Family
ID=4322683
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2220572A Expired GB1381011A (en) | 1971-05-18 | 1972-05-11 | Methylolglycidyl ethers of polyhydric phenol ethers a process for their manufacture and cursable mixtures containing them |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3859255A (enExample) |
| AR (1) | AR193732A1 (enExample) |
| AU (1) | AU461959B2 (enExample) |
| BE (1) | BE783571A (enExample) |
| CA (1) | CA959489A (enExample) |
| CH (1) | CH546234A (enExample) |
| DE (1) | DE2223645A1 (enExample) |
| ES (1) | ES402819A1 (enExample) |
| FR (1) | FR2138007B1 (enExample) |
| GB (1) | GB1381011A (enExample) |
| IT (1) | IT956279B (enExample) |
| NL (1) | NL7206674A (enExample) |
| ZA (1) | ZA723355B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4256844A (en) * | 1976-12-23 | 1981-03-17 | The Dow Chemical Company | Fire retardant, thermosetting, resinous reaction products of phosphoric acid and methyol- or alkoxymethyl-substituted epoxides |
| US4164487A (en) * | 1976-12-23 | 1979-08-14 | The Dow Chemical Company | Water-thinnable mixtures of base-neutralized products of reaction of H3 PO4 with polyether epoxides and with other type epoxides |
| US4284574A (en) * | 1979-06-15 | 1981-08-18 | Ciba-Geigy Corporation | Diglycidyl ethers of di-secondary alcohols, their preparation, and curable compositions containing them |
| US4632973A (en) * | 1985-10-18 | 1986-12-30 | The Dow Chemical Company | Method of improving flame resistance of epoxy resins and resulting compositions |
| KR100367315B1 (ko) * | 1994-06-01 | 2003-03-26 | 스미또모 가가꾸 고오교오 가부시끼가이샤 | 칼라필터의오버코트용경화성수지조성물 |
| EP3548541B1 (en) * | 2016-12-02 | 2022-05-18 | 3M Innovative Properties Company | Dual cure monomers |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2579329A (en) * | 1949-10-18 | 1951-12-18 | Gen Electric | Trimethylol phenol compound and derivatives thereof |
-
1971
- 1971-05-18 CH CH728271A patent/CH546234A/xx not_active IP Right Cessation
-
1972
- 1972-04-25 CA CA140,486A patent/CA959489A/en not_active Expired
- 1972-04-27 AU AU41651/72A patent/AU461959B2/en not_active Expired
- 1972-04-27 US US248279A patent/US3859255A/en not_active Expired - Lifetime
- 1972-05-11 GB GB2220572A patent/GB1381011A/en not_active Expired
- 1972-05-15 DE DE19722223645 patent/DE2223645A1/de active Pending
- 1972-05-16 AR AR242020A patent/AR193732A1/es active
- 1972-05-17 BE BE783571A patent/BE783571A/xx unknown
- 1972-05-17 FR FR727217593A patent/FR2138007B1/fr not_active Expired
- 1972-05-17 ZA ZA723355A patent/ZA723355B/xx unknown
- 1972-05-17 NL NL7206674A patent/NL7206674A/xx unknown
- 1972-05-17 IT IT24494/72A patent/IT956279B/it active
- 1972-05-17 ES ES402819A patent/ES402819A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AR193732A1 (es) | 1973-05-22 |
| FR2138007A1 (enExample) | 1972-12-29 |
| ES402819A1 (es) | 1975-12-16 |
| AU4165172A (en) | 1973-11-01 |
| NL7206674A (enExample) | 1972-11-21 |
| DE2223645A1 (de) | 1972-11-30 |
| BE783571A (fr) | 1972-11-17 |
| FR2138007B1 (enExample) | 1974-07-05 |
| ZA723355B (en) | 1973-02-28 |
| CA959489A (en) | 1974-12-17 |
| IT956279B (it) | 1973-10-10 |
| AU461959B2 (en) | 1975-06-12 |
| CH546234A (de) | 1974-02-28 |
| US3859255A (en) | 1975-01-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3547881A (en) | Process of reacting a phenol with a polyepoxide in the presence of an organic phosphine | |
| US2951825A (en) | Glycidyl derivatives of amino phenols | |
| US2965607A (en) | Ethers of epoxy-substituted phenols and their polymers | |
| GB1392008A (en) | Epoxides derived from triphenylmethane | |
| GB1330932A (en) | Phenolic resin condensation product and light-sensitive compositions containing it | |
| GB1408105A (en) | Curing agent for aqueous epoxide resin dispersions | |
| KR870000317A (ko) | 폴리에폭사이드의 제조방법 | |
| US3100756A (en) | Composition consisting essentially of a polyglycidyl ether and a liquid diepoxide and cured product | |
| US4692504A (en) | Deactivation of phosphonium salt catalyst | |
| GB1515140A (en) | Process for preparing water-dilutable heat-curing coating compositions | |
| GB1381011A (en) | Methylolglycidyl ethers of polyhydric phenol ethers a process for their manufacture and cursable mixtures containing them | |
| US4634757A (en) | Fusion product | |
| GB1488524A (en) | Curing agents for epoxide resins | |
| KR900004796A (ko) | 포스포늄 촉매를 함유하는 에폭시 수지 | |
| GB1487609A (en) | Phosphono-spiro-bisphenols a process for their manufacture and their use | |
| GB1488241A (en) | Process for preparing water-dilutable coating composition | |
| US4732958A (en) | Epoxy fusion process | |
| GB1453881A (en) | Process for the manufacture of glycidyl ethers of monohydric or polyhydric phenols having improved properties | |
| GB1264597A (enExample) | ||
| GB1377246A (en) | Process for the manufacture of of glycidyl-ethers | |
| GB1454345A (en) | Process for the manufacture of polyethers containing ionic bonds | |
| US3033820A (en) | High molecular weight resins | |
| KR870010100A (ko) | 에폭시드기를 함유하는 페놀 에테르 | |
| US3629295A (en) | Glycidyl esters of sterically hindered organic acids | |
| US3360486A (en) | Production of epoxide resins from aromatic amines in the presence of a hydroxyl group-containing promoter |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] |