SE470019B - Monofunktionell akrylatmonomer - Google Patents

Monofunktionell akrylatmonomer

Info

Publication number: SE470019B
Authority: SE; Sweden
Prior art keywords: acrylate monomer; curing; dioxane; methanol; ethyl
Prior art date: 1993-01-20

Application number

SE9300145A

Other languages

English (en)

Swedish (sv)

Other versions

SE9300145D0 (sv

SE9300145L (sv

Inventor

Kent Soerensen

Original Assignee

Perstorp Ab

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.)

1993-01-20

Filing date

1993-01-20

Publication date

1993-10-25

1993-01-20 Application filed by Perstorp Ab filed Critical Perstorp Ab

1993-01-20 Priority to SE9300145A priority Critical patent/SE470019B/sv

1993-01-20 Publication of SE9300145D0 publication Critical patent/SE9300145D0/xx

1993-04-26 Priority to US08/492,053 priority patent/US5559201A/en

1993-04-26 Priority to DE69327338T priority patent/DE69327338T2/de

1993-04-26 Priority to JP6516904A priority patent/JP2764470B2/ja

1993-04-26 Priority to KR1019950702945A priority patent/KR100274584B1/ko

1993-04-26 Priority to PCT/SE1993/000360 priority patent/WO1994017057A1/en

1993-04-26 Priority to CA002152910A priority patent/CA2152910C/en

1993-04-26 Priority to AT93913689T priority patent/ATE187722T1/de

1993-04-26 Priority to EP93913689A priority patent/EP0680477B1/de

1993-04-26 Priority to AU43630/93A priority patent/AU4363093A/en

1993-10-25 Publication of SE9300145L publication Critical patent/SE9300145L/xx

1993-10-25 Publication of SE470019B publication Critical patent/SE470019B/sv

Links

239000000178 monomer Substances 0.000 title claims abstract description 24
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title claims description 21
239000000203 mixture Substances 0.000 claims abstract description 15
238000003847 radiation curing Methods 0.000 claims description 9
239000003973 paint Substances 0.000 claims description 7
239000002966 varnish Substances 0.000 claims description 7
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
239000005548 dental material Substances 0.000 claims description 2
125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
230000005855 radiation Effects 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
239000000047 product Substances 0.000 description 9
238000001723 curing Methods 0.000 description 8
239000004922 lacquer Substances 0.000 description 8
CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 8
206010040880 Skin irritation Diseases 0.000 description 7
238000006243 chemical reaction Methods 0.000 description 7
238000000034 method Methods 0.000 description 7
231100000475 skin irritation Toxicity 0.000 description 7
230000036556 skin irritation Effects 0.000 description 7
BGFBWRWYROQISE-UHFFFAOYSA-N 5-ethyl-1,3-dioxane-5-methanol Chemical compound CCC1(CO)COCOC1 BGFBWRWYROQISE-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 5
239000012071 phase Substances 0.000 description 5
238000010926 purge Methods 0.000 description 5
239000000243 solution Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical class [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
150000001252 acrylic acid derivatives Chemical class 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
239000012965 benzophenone Substances 0.000 description 4
150000008366 benzophenones Chemical class 0.000 description 4
239000003999 initiator Substances 0.000 description 4
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
238000012360 testing method Methods 0.000 description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
238000003848 UV Light-Curing Methods 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
238000005406 washing Methods 0.000 description 3
STGXUBIZGYMIRM-UHFFFAOYSA-N (5-ethyl-1,3-dioxan-5-yl)methyl prop-2-enoate Chemical compound C=CC(=O)OCC1(CC)COCOC1 STGXUBIZGYMIRM-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
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 2
206010015150 Erythema Diseases 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
231100000159 OECD 404 Acute Dermal Irritation/Corrosion Toxicity 0.000 description 2
206010030113 Oedema Diseases 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
230000003078 antioxidant effect Effects 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
238000007865 diluting Methods 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
229910000397 disodium phosphate Inorganic materials 0.000 description 2
235000019800 disodium phosphate Nutrition 0.000 description 2
231100000321 erythema Toxicity 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000009257 reactivity Effects 0.000 description 2
238000010992 reflux Methods 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 1
XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
235000000126 Styrax benzoin Nutrition 0.000 description 1
244000028419 Styrax benzoin Species 0.000 description 1
235000008411 Sumatra benzointree Nutrition 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
150000008062 acetophenones Chemical class 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
238000007664 blowing Methods 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001227 electron beam curing Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
238000005286 illumination Methods 0.000 description 1
238000007373 indentation Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
239000002085 irritant Substances 0.000 description 1
231100000021 irritant Toxicity 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
-1 methacrylate ester Chemical class 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000010959 steel Substances 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
238000012549 training Methods 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F120/10—Esters
- C08F120/12—Esters of monohydric alcohols or phenols
- C08F120/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F120/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F20/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- 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
- C08G65/04—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 only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
- 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
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
Oral & Maxillofacial Surgery (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
General Chemical & Material Sciences (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
Plastic & Reconstructive Surgery (AREA)
Veterinary Medicine (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Polymerisation Methods In General (AREA)
Dental Preparations (AREA)
Paints Or Removers (AREA)
Adhesives Or Adhesive Processes (AREA)
Inks, Pencil-Leads, Or Crayons (AREA)
Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)

SE9300145A 1993-01-20 1993-01-20 Monofunktionell akrylatmonomer SE470019B (sv)

Priority Applications (10)

Application Number	Priority Date	Filing Date	Title
SE9300145A SE470019B (sv)	1993-01-20	1993-01-20	Monofunktionell akrylatmonomer
AU43630/93A AU4363093A (en)	1993-01-20	1993-04-26	Cycloaliphatic acrylic monomer
KR1019950702945A KR100274584B1 (ko)	1993-01-20	1993-04-26	지환식 아크릴 모노머
DE69327338T DE69327338T2 (de)	1993-01-20	1993-04-26	Cycloaliphatische acryloyl-monomere
JP6516904A JP2764470B2 (ja)	1993-01-20	1993-04-26	脂環式アクリルモノマーおよびそれを用いた放射線硬化組成物
US08/492,053 US5559201A (en)	1993-01-20	1993-04-26	Cycloaliphatic acrylic monomer
PCT/SE1993/000360 WO1994017057A1 (en)	1993-01-20	1993-04-26	Cycloaliphatic acrylic monomer
CA002152910A CA2152910C (en)	1993-01-20	1993-04-26	Cycloaliphatic acrylic monomer
AT93913689T ATE187722T1 (de)	1993-01-20	1993-04-26	Cycloaliphatische acryloyl-monomere
EP93913689A EP0680477B1 (de)	1993-01-20	1993-04-26	Cycloaliphatische acryloyl-monomere

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9300145A SE470019B (sv)	1993-01-20	1993-01-20	Monofunktionell akrylatmonomer

Publications (3)

Publication Number	Publication Date
SE9300145D0 SE9300145D0 (sv)	1993-01-20
SE9300145L SE9300145L (sv)	1993-10-25
SE470019B true SE470019B (sv)	1993-10-25

Family

ID=20388589

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9300145A SE470019B (sv)	1993-01-20	1993-01-20	Monofunktionell akrylatmonomer

Country Status (10)

Country	Link
US (1)	US5559201A (de)
EP (1)	EP0680477B1 (de)
JP (1)	JP2764470B2 (de)
KR (1)	KR100274584B1 (de)
AT (1)	ATE187722T1 (de)
AU (1)	AU4363093A (de)
CA (1)	CA2152910C (de)
DE (1)	DE69327338T2 (de)
SE (1)	SE470019B (de)
WO (1)	WO1994017057A1 (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6114458A (en) *	1998-09-23	2000-09-05	International Business Machines Corporation	Highly branched radial block copolymers
JP2006096965A (ja)	2004-02-20	2006-04-13	Tokyo Ohka Kogyo Co Ltd	高分子化合物、該高分子化合物を含有するフォトレジスト組成物、およびレジストパターン形成方法
EP1736485B1 (de) *	2004-04-13	2013-07-31	Tokyo Ohka Kogyo Co., Ltd.	Polymerverbindung, photoresistzusammensetzung mit einer derartigen polymerverbindung und verfahren zur ausbildung einer resiststruktur
JP4799981B2 (ja) *	2005-09-29	2011-10-26	富士フイルム株式会社	インク組成物、インクジェット記録方法、平版印刷版の製造方法、及び平版印刷版
JP4976075B2 (ja) *	2005-12-26	2012-07-18	リンテック株式会社	偏光板用粘着剤、粘着剤付き偏光板及びその製造方法
JP5430051B2 (ja) *	2005-12-28	2014-02-26	富士フイルム株式会社	インク組成物、インクジェット記録方法、平版印刷版の製造方法、及び平版印刷版
US7794918B2 (en)	2005-12-28	2010-09-14	Fujifilm Corporation	Ink composition, inkjet recording method, printed material, method for producing planographic printing plate, and planographic printing plate
JP5490588B2 (ja) *	2010-03-23	2014-05-14	三洋化成工業株式会社	インクジェット印刷インク用重合性化合物及びインク組成物
CN105263939B (zh) *	2013-04-22	2018-04-10	佩什托普公司	用于可辐射固化组合物的具有四氧杂螺旋骨架的丙烯酸类化合物
JP2018035126A (ja) *	2016-09-02	2018-03-08	Dic株式会社	重合性化合物及び光学異方体
EP3326834A1 (de) *	2016-11-23	2018-05-30	Friedrich Klumpp GmbH	Plattenförmiges werkstück, verfahren und anlage zu dessen herstellung, sowie lackzusammensetzung
JP7284635B2 (ja) *	2018-05-30	2023-05-31	住友化学株式会社	樹脂、レジスト組成物及びレジストパターンの製造方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3267084A (en) *	1962-05-23	1966-08-16	Gulf Oil Corp	Polymerizable 5-alkylene-m-dioxanyl acrylic esters
DE1900202A1 (de) *	1969-01-03	1970-08-06	Bayer Ag	Neue Dioxanderivate
DE3208438A1 (de) *	1982-03-09	1983-09-15	Bayer Ag, 5090 Leverkusen	Verfahren zur kantenverfestigung und randabdichtung textiler flaechengebilde
DE58900825D1 (de) *	1988-06-13	1992-03-26	Ciba Geigy Ag	Ungesaettigte beta-ketoesteracetale und ihre anwendungen.
US5004798A (en) *	1989-05-12	1991-04-02	Hoechst Celanese Corporation	Novel polyacetal copolymers of trioxane and trimethylolpropane formal derivatives

1993
- 1993-01-20 SE SE9300145A patent/SE470019B/sv not_active IP Right Cessation
- 1993-04-26 CA CA002152910A patent/CA2152910C/en not_active Expired - Fee Related
- 1993-04-26 EP EP93913689A patent/EP0680477B1/de not_active Expired - Lifetime
- 1993-04-26 AU AU43630/93A patent/AU4363093A/en not_active Abandoned
- 1993-04-26 WO PCT/SE1993/000360 patent/WO1994017057A1/en not_active Ceased
- 1993-04-26 KR KR1019950702945A patent/KR100274584B1/ko not_active Expired - Fee Related
- 1993-04-26 AT AT93913689T patent/ATE187722T1/de not_active IP Right Cessation
- 1993-04-26 DE DE69327338T patent/DE69327338T2/de not_active Expired - Fee Related
- 1993-04-26 JP JP6516904A patent/JP2764470B2/ja not_active Expired - Lifetime
- 1993-04-26 US US08/492,053 patent/US5559201A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
CA2152910C (en)	2001-12-18
KR100274584B1 (ko)	2000-12-15
SE9300145D0 (sv)	1993-01-20
DE69327338D1 (en)	2000-01-20
KR960700241A (ko)	1996-01-19
CA2152910A1 (en)	1994-08-04
SE9300145L (sv)	1993-10-25
EP0680477B1 (de)	1999-12-15
DE69327338T2 (de)	2000-05-18
US5559201A (en)	1996-09-24
ATE187722T1 (de)	2000-01-15
JP2764470B2 (ja)	1998-06-11
EP0680477A1 (de)	1995-11-08
JPH08501108A (ja)	1996-02-06
WO1994017057A1 (en)	1994-08-04
AU4363093A (en)	1994-08-15

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