GB886601A - Improvements in or relating to derivatives of pyromellitic acid, their production and their use as curing agents - Google Patents
Improvements in or relating to derivatives of pyromellitic acid, their production and their use as curing agentsInfo
- Publication number
- GB886601A GB886601A GB40830/59A GB4083059A GB886601A GB 886601 A GB886601 A GB 886601A GB 40830/59 A GB40830/59 A GB 40830/59A GB 4083059 A GB4083059 A GB 4083059A GB 886601 A GB886601 A GB 886601A
- Authority
- GB
- United Kingdom
- Prior art keywords
- glycol
- reacting
- bis
- resin
- epichlorhydrin
- 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
- 239000003795 chemical substances by application Substances 0.000 title abstract 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical class OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 10
- 150000001875 compounds Chemical class 0.000 abstract 7
- -1 hydroxyl radicals Chemical class 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 7
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 6
- 230000001476 alcoholic effect Effects 0.000 abstract 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 abstract 5
- 239000000047 product Substances 0.000 abstract 5
- 150000003254 radicals Chemical class 0.000 abstract 5
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 abstract 4
- 239000003822 epoxy resin Substances 0.000 abstract 4
- 229920000647 polyepoxide Polymers 0.000 abstract 4
- 229920001451 polypropylene glycol Polymers 0.000 abstract 4
- VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 abstract 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 abstract 3
- GRWFFFOEIHGUBG-UHFFFAOYSA-N 3,4-Epoxy-6-methylcyclohexylmethyl-3,4-epoxy-6-methylcyclo-hexanecarboxylate Chemical compound C1C2OC2CC(C)C1C(=O)OCC1CC2OC2CC1C GRWFFFOEIHGUBG-UHFFFAOYSA-N 0.000 abstract 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 abstract 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 3
- KPSSIOMAKSHJJG-UHFFFAOYSA-N neopentyl alcohol Chemical compound CC(C)(C)CO KPSSIOMAKSHJJG-UHFFFAOYSA-N 0.000 abstract 3
- 229920005989 resin Polymers 0.000 abstract 3
- 239000011347 resin Substances 0.000 abstract 3
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 abstract 2
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 abstract 2
- BUEAECUMLINHBK-UHFFFAOYSA-N 2-[2-[[2-(2-hydroxyethoxy)-5-octylphenyl]methyl]-4-octylphenoxy]ethanol Chemical compound OCCOC1=C(C=C(C=C1)CCCCCCCC)CC1=C(C=CC(=C1)CCCCCCCC)OCCO BUEAECUMLINHBK-UHFFFAOYSA-N 0.000 abstract 2
- POIUXCGIAGOITD-UHFFFAOYSA-N 2-[4-[2-[4-(2-hydroxyethyl)phenyl]propan-2-yl]phenyl]ethanol Chemical compound C=1C=C(CCO)C=CC=1C(C)(C)C1=CC=C(CCO)C=C1 POIUXCGIAGOITD-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 244000068988 Glycine max Species 0.000 abstract 2
- 235000010469 Glycine max Nutrition 0.000 abstract 2
- 229920000877 Melamine resin Polymers 0.000 abstract 2
- MFIBZDZRPYQXOM-UHFFFAOYSA-N [dimethyl-[3-(oxiran-2-ylmethoxy)propyl]silyl]oxy-dimethyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound C1OC1COCCC[Si](C)(C)O[Si](C)(C)CCCOCC1CO1 MFIBZDZRPYQXOM-UHFFFAOYSA-N 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
- 239000007859 condensation product Substances 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- 150000002334 glycols Chemical class 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 229920001568 phenolic resin Polymers 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 abstract 1
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 abstract 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 1
- CDBAMNGURPMUTG-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1C(C)(C)C1CCC(O)CC1 CDBAMNGURPMUTG-UHFFFAOYSA-N 0.000 abstract 1
- ZYUVGYBAPZYKSA-UHFFFAOYSA-N 5-(3-hydroxybutan-2-yl)-4-methylbenzene-1,3-diol Chemical compound CC(O)C(C)C1=CC(O)=CC(O)=C1C ZYUVGYBAPZYKSA-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical class CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 abstract 1
- 229920001807 Urea-formaldehyde Polymers 0.000 abstract 1
- YCZZQSFWHFBKMU-UHFFFAOYSA-N [5-(hydroxymethyl)oxolan-2-yl]methanol Chemical compound OCC1CCC(CO)O1 YCZZQSFWHFBKMU-UHFFFAOYSA-N 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000004359 castor oil Substances 0.000 abstract 1
- 235000019438 castor oil Nutrition 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- NHADDZMCASKINP-HTRCEHHLSA-N decarboxydihydrocitrinin Natural products C1=C(O)C(C)=C2[C@H](C)[C@@H](C)OCC2=C1O NHADDZMCASKINP-HTRCEHHLSA-N 0.000 abstract 1
- 125000005442 diisocyanate group Chemical group 0.000 abstract 1
- 150000002118 epoxides Chemical group 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 abstract 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 abstract 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 abstract 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 abstract 1
- 125000003827 glycol group Chemical group 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 abstract 1
- 229920000058 polyacrylate Polymers 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract 1
- 239000005020 polyethylene terephthalate Substances 0.000 abstract 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 abstract 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 1
- 229920002050 silicone resin Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- HQUQLFOMPYWACS-UHFFFAOYSA-N tris(2-chloroethyl) phosphate Chemical compound ClCCOP(=O)(OCCCl)OCCCl HQUQLFOMPYWACS-UHFFFAOYSA-N 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- 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
-
- 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
- C08G59/40—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 curing agents used
- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
- C08G59/4223—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof aromatic
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/123—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/127—Acids containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US886601XA | 1958-12-02 | 1958-12-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB886601A true GB886601A (en) | 1962-01-10 |
Family
ID=22212655
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB40830/59A Expired GB886601A (en) | 1958-12-02 | 1959-12-01 | Improvements in or relating to derivatives of pyromellitic acid, their production and their use as curing agents |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE585234A (enrdf_load_stackoverflow) |
| DE (1) | DE1142699B (enrdf_load_stackoverflow) |
| FR (1) | FR1243591A (enrdf_load_stackoverflow) |
| GB (1) | GB886601A (enrdf_load_stackoverflow) |
| NL (1) | NL245996A (enrdf_load_stackoverflow) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3271476A (en) * | 1962-03-01 | 1966-09-06 | Ciba Ltd | Curable mixtures of epoxy resins and polyanhydrides or polycarboxylic acids |
| WO2005097867A1 (en) * | 2004-04-05 | 2005-10-20 | Az Electronic Materials Usa Corp. | Process for making polyesters |
| US7264913B2 (en) | 2002-11-21 | 2007-09-04 | Az Electronic Materials Usa Corp. | Antireflective compositions for photoresists |
| CN112679704A (zh) * | 2020-12-28 | 2021-04-20 | 陕西科技大学 | 一种潜伏型桥连二酸酐固化剂及其制备方法与应用 |
| CN113583207A (zh) * | 2021-07-01 | 2021-11-02 | 山西省应用化学研究所(有限公司) | 基于蓖麻油的水性聚氨酯乳液及胶粘剂的制备方法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU525570B2 (en) * | 1977-12-07 | 1982-11-11 | Hoechst A.G. | Acid curable epoxy resin composition |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2683131A (en) * | 1951-10-31 | 1954-07-06 | Gen Electric | Acidic polyester-ethoxyline resinous compositions |
| FR1168228A (fr) * | 1955-12-19 | 1958-12-05 | Minnesota Mining & Mfg | Polymérisation de résines d'éthoxyline |
| DE1036518B (de) * | 1956-05-16 | 1958-08-14 | Henkel & Cie Gmbh | Verfahren zur Herstellung von mit Glas- oder Mineralfasern verstaerkten Kunststoffen |
-
0
- BE BE585234D patent/BE585234A/xx unknown
- NL NL245996D patent/NL245996A/xx unknown
-
1959
- 1959-12-01 GB GB40830/59A patent/GB886601A/en not_active Expired
- 1959-12-02 DE DEP24000A patent/DE1142699B/de active Pending
- 1959-12-02 FR FR811950A patent/FR1243591A/fr not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3271476A (en) * | 1962-03-01 | 1966-09-06 | Ciba Ltd | Curable mixtures of epoxy resins and polyanhydrides or polycarboxylic acids |
| US7264913B2 (en) | 2002-11-21 | 2007-09-04 | Az Electronic Materials Usa Corp. | Antireflective compositions for photoresists |
| WO2005097867A1 (en) * | 2004-04-05 | 2005-10-20 | Az Electronic Materials Usa Corp. | Process for making polyesters |
| CN112679704A (zh) * | 2020-12-28 | 2021-04-20 | 陕西科技大学 | 一种潜伏型桥连二酸酐固化剂及其制备方法与应用 |
| CN112679704B (zh) * | 2020-12-28 | 2023-12-12 | 浙江创赢新材料有限公司 | 一种潜伏型桥连二酸酐固化剂及其制备方法与应用 |
| CN113583207A (zh) * | 2021-07-01 | 2021-11-02 | 山西省应用化学研究所(有限公司) | 基于蓖麻油的水性聚氨酯乳液及胶粘剂的制备方法 |
| CN113583207B (zh) * | 2021-07-01 | 2022-08-26 | 山西省应用化学研究所(有限公司) | 基于蓖麻油的水性聚氨酯乳液及胶粘剂的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1243591A (fr) | 1960-10-14 |
| DE1142699B (de) | 1963-01-24 |
| BE585234A (enrdf_load_stackoverflow) | |
| NL245996A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2843560A (en) | Cured silicon-containing products prepared from polyepoxides | |
| US3203920A (en) | Curable mixtures containing epoxy resins, curing agents and flexibilizers | |
| US3668275A (en) | Coating compositions comprising a polyester from 1,4-bis(hydroxymethyl) cyclohexane | |
| US3321445A (en) | Polymers of fluorine-containing sulfonamido polyols | |
| US3904572A (en) | Cold-setting coating composition based on hydroxy-containing vinyl polymer | |
| US3297724A (en) | Diepoxides | |
| US3484408A (en) | Hydroxy-containing imines,their preparation and use as curing agents | |
| US3553284A (en) | Coating compositions comprising a mixture of an aminoplast and a polyester from hexahydroterephthalic acid | |
| US3242142A (en) | Process for curing epoxy resins | |
| GB886601A (en) | Improvements in or relating to derivatives of pyromellitic acid, their production and their use as curing agents | |
| US3471589A (en) | Polyvinyl acetal resins | |
| CA1152531A (en) | Curable epoxide resin mixtures | |
| US4376844A (en) | Hydrocurable ambient curing polyepoxide coating and adhesive compositions and method of using them | |
| US3225065A (en) | Diester compositions formed by the reaction of pyromellitic dianhydride and polyhydric alcohols | |
| US3322797A (en) | Hydroxy containing imine compounds | |
| US3320193A (en) | Hardening of epoxy compounds with trisubstituted triethanol-amine titanates | |
| US3278469A (en) | Interpolymers containing units from a monocarboxylic half ester of an alpha, beta-ethylenically unsaturated, alpha, beta-dicarboxylic acid and coating compositions formulated with these interpolymers | |
| US3293212A (en) | Thermosetting reaction product of hexakis-(alkoxymethyl) melamines and bisphenols | |
| US2226202A (en) | Synthetic resinous materials | |
| US3217035A (en) | Fluorinated polyols | |
| US4028309A (en) | Coating compositions containing esters of dibasic acids, glycols and glycidyl esters, and polyisocyanates | |
| US3242112A (en) | Curable compositions comprising a polymeric bis-cyclopentadienyl compound and a poly-unsaturated material | |
| US3928424A (en) | Mixed esters of dibasic unsaturated acids, glycols and glycidyl esters | |
| US3278488A (en) | Curable mixtures of epoxy resins sulfolene adducts and polyamines | |
| US4308356A (en) | Hydrocurable ambient curing polyepoxide coating and adhesive compositions and method of using same |