SE442294B - Esterdiolalkoxylatakrylater - Google Patents

Esterdiolalkoxylatakrylater

Info

Publication number: SE442294B
Authority: SE; Sweden
Prior art keywords: ester diol; corresponds; acrylate according; ester; structural formula
Prior art date: 1977-09-29

Application number

SE7810204A

Other languages

English (en)

Swedish (sv)

Other versions

SE7810204L (sv

Inventor

R J Knopf

J V Koleske

Original Assignee

Union Carbide Corp

Priority date (The priority date 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 date listed.)

1977-09-29

Filing date

1978-09-28

Publication date

1985-12-16

1978-09-28 Application filed by Union Carbide Corp filed Critical Union Carbide Corp

1979-03-30 Publication of SE7810204L publication Critical patent/SE7810204L/xx

1985-12-16 Publication of SE442294B publication Critical patent/SE442294B/sv

Links

-1 ester ester diol Chemical class 0.000 claims description 66
239000000203 mixture Substances 0.000 claims description 21
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 16
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 12
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000000547 substituted alkyl group Chemical group 0.000 claims 1
238000006243 chemical reaction Methods 0.000 description 23
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical class [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 11
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
239000010410 layer Substances 0.000 description 11
239000000047 product Substances 0.000 description 11
239000003054 catalyst Substances 0.000 description 10
125000002947 alkylene group Chemical group 0.000 description 9
238000005886 esterification reaction Methods 0.000 description 9
229910052757 nitrogen Inorganic materials 0.000 description 9
239000002904 solvent Substances 0.000 description 9
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 9
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
230000032050 esterification Effects 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
230000005855 radiation Effects 0.000 description 8
150000001252 acrylic acid derivatives Chemical class 0.000 description 7
125000004386 diacrylate group Chemical group 0.000 description 7
239000007788 liquid Substances 0.000 description 7
238000000034 method Methods 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
239000011248 coating agent Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
150000002978 peroxides Chemical class 0.000 description 5
SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 description 4
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical class FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
238000001723 curing Methods 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
239000000376 reactant Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
239000002253 acid Substances 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
238000001816 cooling Methods 0.000 description 3
150000002009 diols Chemical class 0.000 description 3
238000004821 distillation Methods 0.000 description 3
239000007888 film coating Substances 0.000 description 3
238000009501 film coating Methods 0.000 description 3
230000005484 gravity Effects 0.000 description 3
239000011261 inert gas Substances 0.000 description 3
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 3
239000000391 magnesium silicate Substances 0.000 description 3
229910052919 magnesium silicate Inorganic materials 0.000 description 3
235000019792 magnesium silicate Nutrition 0.000 description 3
239000012044 organic layer Substances 0.000 description 3
239000012071 phase Substances 0.000 description 3
239000011591 potassium Chemical class 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
230000000717 retained effect Effects 0.000 description 3
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
229910000831 Steel Inorganic materials 0.000 description 2
238000010908 decantation Methods 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000003504 photosensitizing agent Substances 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000003847 radiation curing Methods 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000010959 steel Substances 0.000 description 2
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
CGMDPTNRMYIZTM-NKYSMPERSA-N (2e,4e,6e)-octa-2,4,6-triene Chemical compound C\C=C\C=C\C=C\C CGMDPTNRMYIZTM-NKYSMPERSA-N 0.000 description 1
LYYWLLAXWOGYCY-UHFFFAOYSA-N (4-hydroxy-2,2-dimethylbutyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCCC(C)(C)COC(=O)C(C)(C)CO LYYWLLAXWOGYCY-UHFFFAOYSA-N 0.000 description 1
RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
OHQSQCACEXDHAJ-UHFFFAOYSA-N 2,2-di(butan-2-yloxy)-1-phenylethanone Chemical compound CCC(C)OC(OC(C)CC)C(=O)C1=CC=CC=C1 OHQSQCACEXDHAJ-UHFFFAOYSA-N 0.000 description 1
FXNLOIPXHYYEFS-UHFFFAOYSA-N 2-ethyl-3-hydroxy-5-(hydroxymethyl)-2,5-dimethylheptanoic acid Chemical compound CCC(C)(CO)CC(O)C(C)(CC)C(O)=O FXNLOIPXHYYEFS-UHFFFAOYSA-N 0.000 description 1
FZIIBDOXPQOKBP-UHFFFAOYSA-N 2-methyloxetane Chemical compound CC1CCO1 FZIIBDOXPQOKBP-UHFFFAOYSA-N 0.000 description 1
UTNSRBPPQINCBQ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;oxirane Chemical compound C1CO1.CC(=C)C(O)=O.CC(=C)C(O)=O UTNSRBPPQINCBQ-UHFFFAOYSA-N 0.000 description 1
JBZXHULYWVMNPC-UHFFFAOYSA-N 3-hydroxypropyl 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)C(=O)OCCCO JBZXHULYWVMNPC-UHFFFAOYSA-N 0.000 description 1
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
ZDPLGYATMUWXBN-UHFFFAOYSA-N CC(C)(CCO)CC(CO)C(C)(C)C(O)=O Chemical compound CC(C)(CCO)CC(CO)C(C)(C)C(O)=O ZDPLGYATMUWXBN-UHFFFAOYSA-N 0.000 description 1
LWYMBAVNLIJFRY-UHFFFAOYSA-N CCCC(CCC)(CC(C(CCC)(CCC)C(O)=O)O)CO Chemical compound CCCC(CCC)(CC(C(CCC)(CCC)C(O)=O)O)CO LWYMBAVNLIJFRY-UHFFFAOYSA-N 0.000 description 1
MGPUSNSYXVOTDA-UHFFFAOYSA-N CCCCC(CC)(CC(C(CC)(CCCC)C(O)=O)O)CO Chemical compound CCCCC(CC)(CC(C(CC)(CCCC)C(O)=O)O)CO MGPUSNSYXVOTDA-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
239000002841 Lewis acid Chemical class 0.000 description 1
CGMDPTNRMYIZTM-UHFFFAOYSA-N Sarohornene Natural products CC=CC=CC=CC CGMDPTNRMYIZTM-UHFFFAOYSA-N 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical class COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000011953 free-radical catalyst Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
239000011707 mineral Chemical class 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
RFJIPESEZTVQHZ-UHFFFAOYSA-N oxirane;prop-2-enoic acid Chemical compound C1CO1.OC(=O)C=C RFJIPESEZTVQHZ-UHFFFAOYSA-N 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
239000003973 paint Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000012264 purified product Substances 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000011734 sodium Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical class [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000001029 thermal curing Methods 0.000 description 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2615—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen the other compounds containing carboxylic acid, ester or anhydride groups
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/332—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof
- C08G65/3322—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing carboxyl groups, or halides, or esters thereof acyclic

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Macromonomer-Based Addition Polymer (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Polyethers (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

SE7810204A 1977-09-29 1978-09-28 Esterdiolalkoxylatakrylater SE442294B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/837,839 US4163113A (en)	1977-09-29	1977-09-29	Ester diol alkoxylate acrylates

Publications (2)

Publication Number	Publication Date
SE7810204L SE7810204L (sv)	1979-03-30
SE442294B true SE442294B (sv)	1985-12-16

Family

ID=25275586

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE7810204A SE442294B (sv)	1977-09-29	1978-09-28	Esterdiolalkoxylatakrylater

Country Status (10)

Country	Link
US (1)	US4163113A (it)
JP (1)	JPS5938938B2 (it)
BE (1)	BE870838A (it)
CA (1)	CA1110269A (it)
DE (1)	DE2842305C2 (it)
FR (1)	FR2404623A1 (it)
GB (1)	GB2004868B (it)
IT (1)	IT1099182B (it)
NL (1)	NL7809841A (it)
SE (1)	SE442294B (it)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4377679A (en) *	1982-01-28	1983-03-22	Thiokol Corporation	Photocurable compositions based on acrylate polyester urethanes
JPH0613604B2 (ja) *	1985-03-22	1994-02-23	鐘淵化学工業株式会社	分子末端に不飽和基を含有するポリアルキレンオキシドの製造法
DE3667991D1 (de) *	1985-03-22	1990-02-08	Kanegafuchi Chemical Ind	Polyalkylenoxide mit ungesaettigten endgruppen mit einer begrenzten molekuelmassenverteilung.
JPS624324U (it) *	1985-06-25	1987-01-12
DE3607331A1 (de) *	1986-03-06	1987-09-10	Espe Pharm Praep	(meth)acrylsaeureester und ihre verwendung zur herstellung von dentalmassen
SE9303503D0 (sv) *	1993-10-22	1993-10-22	Perstorp Ab	Acrylic Monomer
DE10131479B4 (de) *	2001-06-29	2005-05-19	Röhm GmbH & Co. KG	Farbstabilisierung von grundstabilisierten ethylenisch ungesättigten Monomeren, insbesondere von grundstabilisierten Hydroxyalkyl(meth)acrylaten

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2542550A (en) *	1947-12-31	1951-02-20	Standard Oil Dev Co	Esters of polyether acids and process
US3645984A (en) *	1969-04-30	1972-02-29	Ppg Industries Inc	Novel acrylic monomers their preparation and treatment
US3959201A (en) *	1972-10-26	1976-05-25	Ppg Industries, Inc.	High solids, water thinnable compositions
DE2500311C2 (de) *	1975-01-07	1983-12-22	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von Propandiol-(1,3)-mono-(3'-hydroxy)-propionaten sowie einige dieser Propandiol-(1,3)-mono-(3'-hydroxy)-propionate

1977
- 1977-09-29 US US05/837,839 patent/US4163113A/en not_active Expired - Lifetime
1978
- 1978-08-28 CA CA310,195A patent/CA1110269A/en not_active Expired
- 1978-09-28 IT IT28196/78A patent/IT1099182B/it active
- 1978-09-28 GB GB7738450A patent/GB2004868B/en not_active Expired
- 1978-09-28 JP JP53118693A patent/JPS5938938B2/ja not_active Expired
- 1978-09-28 BE BE190770A patent/BE870838A/xx not_active IP Right Cessation
- 1978-09-28 NL NL7809841A patent/NL7809841A/xx not_active Application Discontinuation
- 1978-09-28 DE DE2842305A patent/DE2842305C2/de not_active Expired
- 1978-09-28 FR FR7827784A patent/FR2404623A1/fr active Granted
- 1978-09-28 SE SE7810204A patent/SE442294B/sv not_active IP Right Cessation

Also Published As

Publication number	Publication date
DE2842305A1 (de)	1979-04-05
CA1110269A (en)	1981-10-06
JPS5459226A (en)	1979-05-12
SE7810204L (sv)	1979-03-30
IT1099182B (it)	1985-09-18
IT7828196A0 (it)	1978-09-28
US4163113A (en)	1979-07-31
NL7809841A (nl)	1979-04-02
JPS5938938B2 (ja)	1984-09-20
GB2004868B (en)	1982-03-31
FR2404623A1 (fr)	1979-04-27
BE870838A (fr)	1979-03-28
FR2404623B1 (it)	1984-05-11
GB2004868A (en)	1979-04-11
DE2842305C2 (de)	1984-03-29

Legal Events

Date

Code

Title

Description

1995-01-31

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Patent has lapsed

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EP0036813B1 (en)	1984-06-06	(n-substituted carbamoyloxy)alkyleneoxyhydrocarbyl acrylate esters
AU639312B2 (en)	1993-07-22	Vinyl ether compounds
US5159098A (en)	1992-10-27	Alk-1-enyloxy carbamates
US4321406A (en)	1982-03-23	Vinylcyclopropane monomers and oligomers
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EP0151495B1 (en)	1989-02-01	Polyfunctional acrylate derivatives of caprolactone-polyols
US5364691A (en)	1994-11-15	Alk-1-enyloxy carbonates
US5147727A (en)	1992-09-15	Aryloxy polyvinyl ethers
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