IL100971A - Polysulfide polymers that have undergone polymerization with isocyanate - Google Patents

Polysulfide polymers that have undergone polymerization with isocyanate

Info

Publication number: IL100971A
Authority: IL; Israel
Prior art keywords: isocyanate; catalyst; polysulphide; liquid polysulphide; composition
Prior art date: 1991-02-21

Application number

IL10097192A

Other languages

English (en)

Hebrew (he)

Other versions

IL100971A0 (en

Original Assignee

Morton International Ltd

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.)

1991-02-21

Filing date

1992-02-17

Publication date

1994-12-29

1991-02-21 Priority claimed from GB919103670A external-priority patent/GB9103670D0/en

1992-01-03 Priority claimed from GB929200091A external-priority patent/GB9200091D0/en

1992-02-17 Application filed by Morton International Ltd filed Critical Morton International Ltd

1992-11-15 Publication of IL100971A0 publication Critical patent/IL100971A0/xx

1994-12-29 Publication of IL100971A publication Critical patent/IL100971A/en

Links

229920001021 polysulfide Polymers 0.000 title claims description 57
229920000642 polymer Polymers 0.000 title description 25
239000000203 mixture Substances 0.000 claims description 103
239000012948 isocyanate Substances 0.000 claims description 91
150000002513 isocyanates Chemical class 0.000 claims description 75
239000003054 catalyst Substances 0.000 claims description 38
239000004417 polycarbonate Substances 0.000 claims description 35
229920000515 polycarbonate Polymers 0.000 claims description 35
239000007788 liquid Substances 0.000 claims description 33
238000000576 coating method Methods 0.000 claims description 28
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical group CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 26
238000000034 method Methods 0.000 claims description 19
-1 aromatic isocyanate Chemical class 0.000 claims description 17
239000011248 coating agent Substances 0.000 claims description 13
239000003795 chemical substances by application Substances 0.000 claims description 10
229910052751 metal Chemical class 0.000 claims description 8
239000002184 metal Chemical class 0.000 claims description 8
150000003839 salts Chemical class 0.000 claims description 8
239000006229 carbon black Substances 0.000 claims description 7
239000006087 Silane Coupling Agent Substances 0.000 claims description 6
239000000178 monomer Substances 0.000 claims description 6
125000002524 organometallic group Chemical class 0.000 claims description 6
239000000565 sealant Substances 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 5
239000012975 dibutyltin dilaurate Substances 0.000 claims description 5
239000011347 resin Substances 0.000 claims description 5
229920005989 resin Polymers 0.000 claims description 5
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 5
239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 4
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical group O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 4
239000011342 resin composition Substances 0.000 claims description 3
235000010290 biphenyl Nutrition 0.000 claims 2
239000004305 biphenyl Substances 0.000 claims 2
125000006267 biphenyl group Chemical group 0.000 claims 2
POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 claims 2
229940070765 laurate Drugs 0.000 claims 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
239000007767 bonding agent Substances 0.000 claims 1
NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 33
238000012360 testing method Methods 0.000 description 28
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 27
238000001723 curing Methods 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
238000009472 formulation Methods 0.000 description 17
229940099594 manganese dioxide Drugs 0.000 description 16
230000001070 adhesive effect Effects 0.000 description 13
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000000853 adhesive Substances 0.000 description 12
239000011521 glass Substances 0.000 description 11
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 10
230000000694 effects Effects 0.000 description 10
239000010408 film Substances 0.000 description 10
239000004570 mortar (masonry) Substances 0.000 description 10
239000010409 thin film Substances 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 8
238000005299 abrasion Methods 0.000 description 7
PGYPOBZJRVSMDS-UHFFFAOYSA-N loperamide hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)N(C)C)CCN(CC1)CCC1(O)C1=CC=C(Cl)C=C1 PGYPOBZJRVSMDS-UHFFFAOYSA-N 0.000 description 7
230000000704 physical effect Effects 0.000 description 7
239000000463 material Substances 0.000 description 6
230000035882 stress Effects 0.000 description 6
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 5
239000004433 Thermoplastic polyurethane Substances 0.000 description 5
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
229910052748 manganese Inorganic materials 0.000 description 5
239000011572 manganese Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
229920002803 thermoplastic polyurethane Polymers 0.000 description 5
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
230000032683 aging Effects 0.000 description 4
230000008859 change Effects 0.000 description 4
229910000077 silane Inorganic materials 0.000 description 4
239000006244 Medium Thermal Substances 0.000 description 3
239000002313 adhesive film Substances 0.000 description 3
239000004411 aluminium Substances 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
230000000903 blocking effect Effects 0.000 description 3
238000007654 immersion Methods 0.000 description 3
238000007789 sealing Methods 0.000 description 3
239000000758 substrate Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 2
LDOVVUQNRISGKB-UHFFFAOYSA-N [N-]=C=O.[O-2].[O-2].[Mn+5] Chemical compound [N-]=C=O.[O-2].[O-2].[Mn+5] LDOVVUQNRISGKB-UHFFFAOYSA-N 0.000 description 2
230000002411 adverse Effects 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
238000007664 blowing Methods 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
229910002092 carbon dioxide Inorganic materials 0.000 description 2
239000008199 coating composition Substances 0.000 description 2
238000007906 compression Methods 0.000 description 2
230000006835 compression Effects 0.000 description 2
238000007596 consolidation process Methods 0.000 description 2
230000032798 delamination Effects 0.000 description 2
239000000945 filler Substances 0.000 description 2
239000000446 fuel Substances 0.000 description 2
230000005484 gravity Effects 0.000 description 2
230000006872 improvement Effects 0.000 description 2
230000007774 longterm Effects 0.000 description 2
230000007246 mechanism Effects 0.000 description 2
239000002808 molecular sieve Substances 0.000 description 2
239000004814 polyurethane Substances 0.000 description 2
229920002635 polyurethane Polymers 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
229920013730 reactive polymer Polymers 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
229910052725 zinc Inorganic materials 0.000 description 2
239000011701 zinc Substances 0.000 description 2
NLXGURFLBLRZRO-UHFFFAOYSA-N 1-chloro-2-(2-chloroethoxymethoxy)ethane Chemical compound ClCCOCOCCCl NLXGURFLBLRZRO-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000005266 casting Methods 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
238000013007 heat curing Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002696 manganese Chemical class 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical group C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
XMGMFRIEKMMMSU-UHFFFAOYSA-N phenylmethylbenzene Chemical group C=1C=CC=CC=1[C]C1=CC=CC=C1 XMGMFRIEKMMMSU-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000011417 postcuring Methods 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
239000013557 residual solvent Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000009864 tensile test Methods 0.000 description 1
238000002076 thermal analysis method Methods 0.000 description 1
KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
238000012546 transfer Methods 0.000 description 1
HFFZSMFXOBHQLV-UHFFFAOYSA-M tributylstannyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)CCCC HFFZSMFXOBHQLV-UHFFFAOYSA-M 0.000 description 1
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/64—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63
- C08G18/6453—Macromolecular compounds not provided for by groups C08G18/42 - C08G18/63 having sulfur
- 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
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
- C08G18/244—Catalysts containing metal compounds of tin tin salts of carboxylic acids
- C08G18/246—Catalysts containing metal compounds of tin tin salts of carboxylic acids containing also tin-carbon bonds
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Polyurethanes Or Polyureas (AREA)
Paints Or Removers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

IL10097192A 1991-02-21 1992-02-17 Polysulfide polymers that have undergone polymerization with isocyanate IL100971A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB919103670A GB9103670D0 (en)	1991-02-21	1991-02-21	Isocyanate-cured polysulphide polymers
GB929200091A GB9200091D0 (en)	1992-01-03	1992-01-03	Adhesive,sealing and coating compositions comprising cured polysulphide polymers

Publications (2)

Publication Number	Publication Date
IL100971A0 IL100971A0 (en)	1992-11-15
IL100971A true IL100971A (en)	1994-12-29

Family

ID=26298474

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10097192A IL100971A (en)	1991-02-21	1992-02-17	Polysulfide polymers that have undergone polymerization with isocyanate

Country Status (8)

Country	Link
US (1)	US5212231A (fr)
EP (1)	EP0500335A3 (fr)
JP (1)	JPH06228312A (fr)
AU (1)	AU652991B2 (fr)
CA (1)	CA2061597C (fr)
IL (1)	IL100971A (fr)
MX (1)	MX9200710A (fr)
NZ (1)	NZ241669A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5319057A (en) *	1990-12-07	1994-06-07	Toray Thiokol Co., Ltd.	Curable composition containing a polysulfide polyether and a compound having at least two isocyanate groups
US20090220700A1 (en) *	2008-02-28	2009-09-03	Carl Peres	Coating Composition And Method Of Application
US7875666B2 (en) *	2008-04-24	2011-01-25	Prc-De Soto International, Inc.	Thioethers, methods for their preparation, and compositions including such thioethers
EP3601404B1 (fr) *	2017-03-28	2024-04-03	Covestro Deutschland AG	Mousse polyuréthane translucide

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3077464A (en) *	1954-09-13	1963-02-12	Lockheed Aircraft Corp	Composition comprising a polyisocyanate reaction product and a polysulfide polymer
DE1050474B (de) *	1956-12-14	1959-02-12	Phoenix Gummiwerke Aktiengesellschaft Hamburg - Harburg	Lacke fur Kautschukartikel
US4349656A (en) *	1980-07-23	1982-09-14	American Cyanamid Company	Thiodiethanol based polyurethane elastomers having improved dynamic properties and method for production thereof
US4345053A (en) *	1981-07-17	1982-08-17	Essex Chemical Corp.	Silicon-terminated polyurethane polymer
GB8612401D0 (en) *	1986-05-21	1986-06-25	Evode Ltd	Liquid polmers
JPH0788416B2 (ja) *	1986-12-10	1995-09-27	東レチオコール株式会社	硬化型組成物
JP2633029B2 (ja) *	1989-08-01	1997-07-23	東レチオコール株式会社	硬化型組成物
CA2024596C (fr) *	1989-09-11	1997-08-19	James D. Nichols	Catalyseurs a base de compose organique de l'etain, utilisables dans des systemes de polyurethane
EP0423642A3 (en) *	1989-10-20	1991-07-03	Air Products And Chemicals, Inc.	Polymeric diorganotin catalysts for use in polyurethane systems

1992
- 1992-02-14 AU AU10962/92A patent/AU652991B2/en not_active Ceased
- 1992-02-17 IL IL10097192A patent/IL100971A/en not_active IP Right Cessation
- 1992-02-19 EP EP19920301347 patent/EP0500335A3/en not_active Withdrawn
- 1992-02-20 MX MX9200710A patent/MX9200710A/es not_active IP Right Cessation
- 1992-02-20 NZ NZ241669A patent/NZ241669A/en unknown
- 1992-02-20 CA CA002061597A patent/CA2061597C/fr not_active Expired - Fee Related
- 1992-02-20 JP JP4033021A patent/JPH06228312A/ja active Pending
- 1992-02-20 US US07/839,517 patent/US5212231A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPH06228312A (ja)	1994-08-16
US5212231A (en)	1993-05-18
AU652991B2 (en)	1994-09-15
EP0500335A2 (fr)	1992-08-26
MX9200710A (es)	1992-09-01
IL100971A0 (en)	1992-11-15
CA2061597C (fr)	1997-01-14
EP0500335A3 (en)	1993-01-07
NZ241669A (en)	1993-06-25
AU1096292A (en)	1992-08-27
CA2061597A1 (fr)	1992-08-22

Legal Events

Date	Code	Title	Description
1998-08-16	KB	Patent renewed
2006-10-30	MM9K	Patent not in force due to non-payment of renewal fees

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