JPS5863771A - 安定したシアノアクリル酸塩接着剤の組成物とその製法 - Google Patents

安定したシアノアクリル酸塩接着剤の組成物とその製法

Info

Publication number: JPS5863771A
Authority: JP; Japan
Prior art keywords: acid; weight; composition; concentration; present
Prior art date: 1981-09-30
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.): Pending

Application number

JP15837681A

Other languages

English (en)

Japanese (ja)

Inventor

ルイス・ア−ル・リザルデイ

バ−ナ−ド・マロフスキ−

クリス・マリオツテイ

ジユ−・チヤオ・リユ

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Henkel Loctite Corp

Original Assignee

Henkel Loctite 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.)

1981-09-30

Filing date

1981-10-05

Publication date

1983-04-15

1981-10-05 Application filed by Henkel Loctite Corp filed Critical Henkel Loctite Corp

1983-04-15 Publication of JPS5863771A publication Critical patent/JPS5863771A/ja

Status Pending legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 68
239000004830 Super Glue Substances 0.000 title claims description 12
FGBJXOREULPLGL-UHFFFAOYSA-N ethyl cyanoacrylate Chemical compound CCOC(=O)C(=C)C#N FGBJXOREULPLGL-UHFFFAOYSA-N 0.000 title claims description 11
238000004519 manufacturing process Methods 0.000 title description 6
239000002253 acid Substances 0.000 claims description 50
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 24
IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 claims description 16
239000003112 inhibitor Substances 0.000 claims description 12
229940098779 methanesulfonic acid Drugs 0.000 claims description 12
229920001651 Cyanoacrylate Polymers 0.000 claims description 11
MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 claims description 11
150000002148 esters Chemical class 0.000 claims description 11
239000000178 monomer Substances 0.000 claims description 11
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 9
-1 cycloargyl Chemical group 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 6
230000002378 acidificating effect Effects 0.000 claims description 5
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
230000008569 process Effects 0.000 claims description 4
125000003342 alkenyl group Chemical group 0.000 claims description 3
VJVNWXUZZOBHRZ-UHFFFAOYSA-N benzene phosphoric acid Chemical compound P(=O)(O)(O)O.P(=O)(O)(O)O.P(=O)(O)(O)O.C1=CC=CC=C1 VJVNWXUZZOBHRZ-UHFFFAOYSA-N 0.000 claims description 3
125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
235000006408 oxalic acid Nutrition 0.000 claims description 3
238000010526 radical polymerization reaction Methods 0.000 claims description 3
MEXUTNIFSHFQRG-UHFFFAOYSA-N 6,7,12,13-tetrahydro-5h-indolo[2,3-a]pyrrolo[3,4-c]carbazol-5-one Chemical group C12=C3C=CC=C[C]3NC2=C2NC3=CC=C[CH]C3=C2C2=C1C(=O)NC2 MEXUTNIFSHFQRG-UHFFFAOYSA-N 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
CLHYKAZPWIRRRD-UHFFFAOYSA-N 1-hydroxypropane-1-sulfonic acid Chemical compound CCC(O)S(O)(=O)=O CLHYKAZPWIRRRD-UHFFFAOYSA-N 0.000 claims 2
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 2
MIAUJDCQDVWHEV-UHFFFAOYSA-N benzene-1,2-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1S(O)(=O)=O MIAUJDCQDVWHEV-UHFFFAOYSA-N 0.000 claims 1
QICVZJNIJUZAGZ-UHFFFAOYSA-N benzene;phosphorous acid Chemical compound OP(O)O.C1=CC=CC=C1 QICVZJNIJUZAGZ-UHFFFAOYSA-N 0.000 claims 1
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
125000002843 carboxylic acid group Chemical group 0.000 claims 1
230000001070 adhesive effect Effects 0.000 description 22
239000000853 adhesive Substances 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
239000003381 stabilizer Substances 0.000 description 15
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 12
150000007513 acids Chemical class 0.000 description 11
239000007789 gas Substances 0.000 description 9
230000002195 synergetic effect Effects 0.000 description 9
230000000694 effects Effects 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
239000004698 Polyethylene Substances 0.000 description 5
230000000996 additive effect Effects 0.000 description 5
238000010539 anionic addition polymerization reaction Methods 0.000 description 5
229920000573 polyethylene Polymers 0.000 description 5
230000000087 stabilizing effect Effects 0.000 description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 4
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
229910052782 aluminium Inorganic materials 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000002562 thickening agent Substances 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
150000004677 hydrates Chemical class 0.000 description 3
239000004014 plasticizer Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000006482 condensation reaction Methods 0.000 description 2
MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 2
238000004821 distillation Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
239000012535 impurity Substances 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000004033 plastic Substances 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
238000003860 storage Methods 0.000 description 2
AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
LZCZEOOJQGXTAF-UHFFFAOYSA-N 1-hydroxypropane-1-sulfinic acid Chemical compound CCC(O)S(O)=O LZCZEOOJQGXTAF-UHFFFAOYSA-N 0.000 description 1
XESZUVZBAMCAEJ-UHFFFAOYSA-N 4-tert-butylcatechol Chemical compound CC(C)(C)C1=CC=C(O)C(O)=C1 XESZUVZBAMCAEJ-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
229910015900 BF3 Inorganic materials 0.000 description 1
241000255925 Diptera Species 0.000 description 1
241000283074 Equus asinus Species 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
241000270666 Testudines Species 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
239000000654 additive Substances 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
229910052796 boron Inorganic materials 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
235000010980 cellulose Nutrition 0.000 description 1
229920006217 cellulose acetate butyrate Polymers 0.000 description 1
229920001727 cellulose butyrate Polymers 0.000 description 1
230000008859 change Effects 0.000 description 1
238000005336 cracking Methods 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229940053009 ethyl cyanoacrylate Drugs 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000004508 fractional distillation Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
235000012907 honey Nutrition 0.000 description 1
229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920001289 polyvinyl ether Polymers 0.000 description 1
238000004382 potting Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000000021 stimulant Substances 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
239000010409 thin film Substances 0.000 description 1
238000010792 warming Methods 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- 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)
Adhesives Or Adhesive Processes (AREA)

JP15837681A 1981-09-30 1981-10-05 安定したシアノアクリル酸塩接着剤の組成物とその製法 Pending JPS5863771A (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
BE0/206109A BE890553A (fr)	1981-09-30	1981-09-30	Compositions a base de cyano-acrylates stabilisees

Publications (1)

Publication Number	Publication Date
JPS5863771A true JPS5863771A (ja)	1983-04-15

Family

ID=3843456

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP15837681A Pending JPS5863771A (ja)	1981-09-30	1981-10-05	安定したシアノアクリル酸塩接着剤の組成物とその製法

Country Status (7)

Country	Link
JP (1)	JPS5863771A (fr)
AU (1)	AU7565681A (fr)
BE (1)	BE890553A (fr)
CA (1)	CA1162562A (fr)
DE (1)	DE3140246A1 (fr)
FR (1)	FR2515196A1 (fr)
GB (1)	GB2107328B (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6131480A (ja) *	1984-07-25	1986-02-13	Okura Ind Co Ltd	α−シアノアクリレ−ト系接着剤組成物
JP2007126632A (ja) *	2005-10-06	2007-05-24	Taoka Chem Co Ltd	２−シアノアクリレート系接着剤組成物
JP2010189512A (ja) *	2009-02-17	2010-09-02	Taoka Chem Co Ltd	２−シアノアクリレート系接着剤組成物

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6099182A (ja) *	1983-11-04	1985-06-03	Atsugi Chuo Kenkyusho Kk	シアノアクリレート混合用金属粉
DE3414805A1 (de) *	1984-04-19	1985-10-24	Bayer Ag, 5090 Leverkusen	Stabilisierte klebstoffe
DE4135116A1 (de) *	1991-10-24	1993-04-29	Henkel Kgaa	Lagerstabiler cyanoacrylat-klebstoff in al-tuben
DE4229640C2 (de) *	1992-09-04	1996-11-21	Tomas Meinen	Verfahren zum Auftragen von Cyanacrylat-Klebstoffen
PL310073A1 (en) *	1993-01-11	1995-11-27	Eurotax Ltd	Method of obtaining 2-cyanoacrylic esters and application of so obtained esters and application of so obtained esters as gluess
US5480935A (en)	1994-09-01	1996-01-02	Medlogic Global Corporation	Cyanoacrylate adhesive compositions
US6512023B1 (en)	1998-06-18	2003-01-28	Closure Medical Corporation	Stabilized monomer adhesive compositions
US6605667B1 (en)	2000-09-08	2003-08-12	Closure Medical Corporation	Antioxidant enriched adhesive compositions and storage containers therefor
US6779657B2 (en)	2001-06-06	2004-08-24	Closure Medical Corporation	Single-use applicators, dispensers and methods for polymerizable monomer compound
WO2003105696A1 (fr)	2001-06-06	2003-12-24	Closure Medical Corporation	Applicateurs a usage unique, distributeurs et procede destine a un compose de monomere polymerisable
US6811341B2 (en)	2001-08-16	2004-11-02	Closure Medical Corporation	Multiple-component combining
US6547467B2 (en)	2001-08-29	2003-04-15	Closure Medical Corporation	Microapplicators, delivery systems and methods for adhesives and sealants
JP6404707B2 (ja) *	2014-01-06	2018-10-10	日東電工株式会社	アクリル系粘着剤組成物、アクリル系粘着剤層、粘着剤層付き基材フィルム、積層体、及び画像表示装置

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4125494A (en) *	1977-08-12	1978-11-14	National Starch And Chemical Corporation	Adhesion promoter for 2-cyanoacrylate adhesive compositions

1981
- 1981-09-22 CA CA000386395A patent/CA1162562A/fr not_active Expired
- 1981-09-25 AU AU75656/81A patent/AU7565681A/en not_active Abandoned
- 1981-09-30 BE BE0/206109A patent/BE890553A/fr not_active IP Right Cessation
- 1981-10-05 JP JP15837681A patent/JPS5863771A/ja active Pending
- 1981-10-08 GB GB08130491A patent/GB2107328B/en not_active Expired
- 1981-10-09 DE DE19813140246 patent/DE3140246A1/de not_active Ceased
- 1981-10-23 FR FR8119951A patent/FR2515196A1/fr active Granted

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6131480A (ja) *	1984-07-25	1986-02-13	Okura Ind Co Ltd	α−シアノアクリレ−ト系接着剤組成物
JP2007126632A (ja) *	2005-10-06	2007-05-24	Taoka Chem Co Ltd	２−シアノアクリレート系接着剤組成物
JP2010189512A (ja) *	2009-02-17	2010-09-02	Taoka Chem Co Ltd	２−シアノアクリレート系接着剤組成物

Also Published As

Publication number	Publication date
CA1162562A (fr)	1984-02-21
GB2107328B (en)	1985-05-01
BE890553A (fr)	1982-03-30
FR2515196B1 (fr)	1984-12-28
DE3140246A1 (de)	1983-04-28
AU7565681A (en)	1983-03-31
GB2107328A (en)	1983-04-27
FR2515196A1 (fr)	1983-04-29

Publication	Publication Date	Title
JPS5863771A (ja)	1983-04-15	安定したシアノアクリル酸塩接着剤の組成物とその製法
US4182823A (en)	1980-01-08	Anionic polymerization inhibitor for cyanoacrylate adhesives
US5089051A (en)	1992-02-18	Adhesion-promoting dental composition
US3742018A (en)	1973-06-26	Cyanoacrylate adhesive composition
DE2201549A1 (de)	1973-08-02	Cyanoacrylat-klebstoffmassen mit verbesserter waermebestaendigkeit
CA2310421A1 (fr)	1999-05-27	Colles de cyano-acrylate stabilisees
US4034145A (en)	1977-07-05	Anaerobically hardening adhesives and sealants containing an organic percarboxylic acids
JPH0350724B2 (fr)	1991-08-02
EP1940340B1 (fr)	2014-05-21	Adhésif dentaire
SU559655A3 (ru)	1977-05-25	Клей
US2255483A (en)	1941-09-09	Inhibited polymerizable unsaturated organic compound
US3988507A (en)	1976-10-26	Anaerobically hardening adhesives and sealants containing a hydrazone accelerator
US3985943A (en)	1976-10-12	Anaerobically hardening adhesives and sealants containing organic disulfonamides
IE51599B1 (en)	1987-01-21	STABILISED CYANOACRYLATE ADHESIVE COMPOSITION IE
US3577394A (en)	1971-05-04	2-chloroethyl 2-cyanoacrylate and compositions thereof
US2407143A (en)	1946-09-03	Adhesives and a process of producing same
SU1574618A1 (ru)	1990-06-30	Клеева композици
JPH04124168A (ja)	1992-04-24	α―シアノアクリレート類の製造方法
US3984385A (en)	1976-10-05	Anaerobically hardening adhesives and sealants containing a hydrazide accelerator
US20090048367A1 (en)	2009-02-19	Dental adhesive
US3987234A (en)	1976-10-19	Anaerobically hardening adhesives and sealants containing an organic hydrazines
JP2919103B2 (ja)	1999-07-12	嫌気性接着剤の改良
SU668332A1 (ru)	1983-11-15	Клеева композици
JPH0149169B2 (fr)	1989-10-23
RU2043385C1 (ru)	1995-09-10	Анаэробная композиция

JPS5863771A - 安定したシアノアクリル酸塩接着剤の組成物とその製法 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (1)

Publications (1)

Family

ID=3843456

Family Applications (1)

Country Status (7)

Cited By (3)

Families Citing this family (13)

Family Cites Families (1)

Cited By (3)

Also Published As

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