IL97423A - Esters Bite (Tribromoniophentyl) of flame retardant orthopedic acid and plastic and rubber preparations containing them - Google Patents

Esters Bite (Tribromoniophentyl) of flame retardant orthopedic acid and plastic and rubber preparations containing them

Info

Publication number: IL97423A
Authority: IL; Israel
Prior art keywords: flame retardant; esters; bis; tribromoneopentyl; formula
Prior art date: 1990-03-05

Application number

IL9742391A

Other languages

English (en)

Hebrew (he)

Other versions

IL97423A0 (en

Original Assignee

Ass Octel

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.)

1990-03-05

Filing date

1991-03-04

Publication date

1994-12-29

1991-03-04 Application filed by Ass Octel filed Critical Ass Octel

1992-06-21 Publication of IL97423A0 publication Critical patent/IL97423A0/xx

1994-12-29 Publication of IL97423A publication Critical patent/IL97423A/en

Links

239000003063 flame retardant Substances 0.000 title claims abstract description 35
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 29
150000002148 esters Chemical class 0.000 title claims abstract description 15
239000000203 mixture Substances 0.000 title claims description 16
-1 tribromoneopentyl Chemical group 0.000 title claims description 15
229920001971 elastomer Polymers 0.000 title claims description 8
229920003023 plastic Polymers 0.000 title claims description 8
239000004033 plastic Substances 0.000 title claims description 8
239000005060 rubber Substances 0.000 title claims description 8
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 title abstract description 3
QEJPOEGPNIVDMK-UHFFFAOYSA-N 3-bromo-2,2-bis(bromomethyl)propan-1-ol Chemical compound OCC(CBr)(CBr)CBr QEJPOEGPNIVDMK-UHFFFAOYSA-N 0.000 claims abstract description 4
150000001875 compounds Chemical class 0.000 claims description 25
229920005669 high impact polystyrene Polymers 0.000 claims description 9
239000004797 high-impact polystyrene Substances 0.000 claims description 9
239000004743 Polypropylene Substances 0.000 claims description 7
238000006243 chemical reaction Methods 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
238000010992 reflux Methods 0.000 claims description 7
150000008064 anhydrides Chemical class 0.000 claims description 5
239000000463 material Substances 0.000 claims description 5
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 4
150000008065 acid anhydrides Chemical class 0.000 claims description 4
229910000410 antimony oxide Inorganic materials 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
229920001155 polypropylene Polymers 0.000 claims description 3
229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims 1
229920000728 polyester Polymers 0.000 abstract description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 25
229920000642 polymer Polymers 0.000 description 13
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 9
239000000654 additive Substances 0.000 description 9
239000000047 product Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
125000003118 aryl group Chemical group 0.000 description 6
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
239000004793 Polystyrene Substances 0.000 description 4
238000004458 analytical method Methods 0.000 description 4
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
229920002223 polystyrene Polymers 0.000 description 4
239000004814 polyurethane Substances 0.000 description 4
229920002635 polyurethane Polymers 0.000 description 4
VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
229920006351 engineering plastic Polymers 0.000 description 3
238000000197 pyrolysis Methods 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
AOJDZKCUAATBGE-UHFFFAOYSA-N bromomethane Chemical compound Br[CH2] AOJDZKCUAATBGE-UHFFFAOYSA-N 0.000 description 2
238000013329 compounding Methods 0.000 description 2
238000000748 compression moulding Methods 0.000 description 2
229920003247 engineering thermoplastic Polymers 0.000 description 2
125000004185 ester group Chemical group 0.000 description 2
239000012065 filter cake Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
239000004926 polymethyl methacrylate Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
239000000523 sample Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
229920003048 styrene butadiene rubber Polymers 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
KVGZZAHHUNAVKZ-UHFFFAOYSA-N 1,4-Dioxin Chemical compound O1C=COC=C1 KVGZZAHHUNAVKZ-UHFFFAOYSA-N 0.000 description 1
WZHHYIOUKQNLQM-UHFFFAOYSA-N 3,4,5,6-tetrachlorophthalic acid Chemical class OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(O)=O WZHHYIOUKQNLQM-UHFFFAOYSA-N 0.000 description 1
XQMVBICWFFHDNN-UHFFFAOYSA-N 5-amino-4-chloro-2-phenylpyridazin-3-one;(2-ethoxy-3,3-dimethyl-2h-1-benzofuran-5-yl) methanesulfonate Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1.C1=C(OS(C)(=O)=O)C=C2C(C)(C)C(OCC)OC2=C1 XQMVBICWFFHDNN-UHFFFAOYSA-N 0.000 description 1
241000905957 Channa melasoma Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
KZCBXHSWMMIEQU-UHFFFAOYSA-N Chlorthal Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(C(O)=O)C(Cl)=C1Cl KZCBXHSWMMIEQU-UHFFFAOYSA-N 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
229920005439 Perspex® Polymers 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
QHWKHLYUUZGSCW-UHFFFAOYSA-N Tetrabromophthalic anhydride Chemical compound BrC1=C(Br)C(Br)=C2C(=O)OC(=O)C2=C1Br QHWKHLYUUZGSCW-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229920006243 acrylic copolymer Polymers 0.000 description 1
XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001463 antimony compounds Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
238000007080 aromatic substitution reaction Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
RGAXKNXQQAXGMM-UHFFFAOYSA-N bis(1,1,3-tribromo-2,2-dimethylpropyl) 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate Chemical compound BrCC(C)(C)C(Br)(Br)OC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC(Br)(Br)C(C)(C)CBr)C(Cl)=C1Cl RGAXKNXQQAXGMM-UHFFFAOYSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
230000031709 bromination Effects 0.000 description 1
238000005893 bromination reaction Methods 0.000 description 1
125000005997 bromomethyl group Chemical group 0.000 description 1
229920005549 butyl rubber Polymers 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
230000001413 cellular effect Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
229920006248 expandable polystyrene Polymers 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
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 description 1
229920001519 homopolymer Polymers 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
229910001026 inconel Inorganic materials 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001955 polyphenylene ether Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
238000010998 test method Methods 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/12—Esters; Ether-esters of cyclic polycarboxylic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/75—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a six-membered ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/80—Phthalic acid esters

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Fireproofing Substances (AREA)
Polyesters Or Polycarbonates (AREA)

IL9742391A 1990-03-05 1991-03-04 Esters Bite (Tribromoniophentyl) of flame retardant orthopedic acid and plastic and rubber preparations containing them IL97423A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB909004857A GB9004857D0 (en)	1990-03-05	1990-03-05	Flame retardant compounds and compositions containing them

Publications (2)

Publication Number	Publication Date
IL97423A0 IL97423A0 (en)	1992-06-21
IL97423A true IL97423A (en)	1994-12-29

Family

ID=10671999

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9742391A IL97423A (en)	1990-03-05	1991-03-04	Esters Bite (Tribromoniophentyl) of flame retardant orthopedic acid and plastic and rubber preparations containing them

Country Status (9)

Country	Link
US (1)	US5393820A (fr)
EP (1)	EP0446003B1 (fr)
AT (1)	ATE109762T1 (fr)
DE (1)	DE69103296T2 (fr)
DK (1)	DK0446003T3 (fr)
ES (1)	ES2060294T3 (fr)
GB (1)	GB9004857D0 (fr)
IL (1)	IL97423A (fr)
WO (1)	WO1991013858A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9127588D0 (en) *	1991-12-24	1992-02-19	Ciba Geigy Ag	Flame retardant compounds
US5824241A (en) *	1997-05-19	1998-10-20	Albemarle Corporation	Brominated tetrabromophthalate ester flame retardants flame retardant polymer compositions
EP1012133A4 (fr) *	1997-06-18	2000-08-30	Great Lakes Chemical Corp	Nouveaux plastifiants ignifuges
US20040209967A1 (en) *	2003-04-21	2004-10-21	Ranken Paul F.	Flame retarded styrenic polymer foams

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3772342A (en) *	1970-12-16	1973-11-13	Hercules Inc	Polycarboxylic acid esters of halogen containing alcohols
DE3034634C2 (de) *	1980-09-13	1982-11-11	Chemische Fabrik Kalk GmbH, 5000 Köln	Tetrabromphthalsäureester, Herstellung und Verwendung als Brandschutzmittel in Kunststoffen
US4764550A (en) *	1985-09-17	1988-08-16	Pennwalt Corporation	Tetrahalophthalate esters as flame retardants for polyphenylene ether resins
EP0297112A4 (fr) *	1986-11-14	1989-04-24	Great Lakes Chemical Corp	Ethers de polyphenylenes modifies a inflammation retardee possedant des caracteristiques d'ecoulement ameliorees.

1990
- 1990-03-05 GB GB909004857A patent/GB9004857D0/en active Pending
1991
- 1991-03-04 IL IL9742391A patent/IL97423A/en not_active IP Right Cessation
- 1991-03-04 DK DK91301784.4T patent/DK0446003T3/da active
- 1991-03-04 AT AT91301784T patent/ATE109762T1/de not_active IP Right Cessation
- 1991-03-04 WO PCT/GB1991/000322 patent/WO1991013858A1/fr not_active Ceased
- 1991-03-04 DE DE69103296T patent/DE69103296T2/de not_active Expired - Fee Related
- 1991-03-04 ES ES91301784T patent/ES2060294T3/es not_active Expired - Lifetime
- 1991-03-04 US US07/934,432 patent/US5393820A/en not_active Expired - Fee Related
- 1991-03-04 EP EP91301784A patent/EP0446003B1/fr not_active Expired - Lifetime

Also Published As

Publication number	Publication date
ES2060294T3 (es)	1994-11-16
ATE109762T1 (de)	1994-08-15
DE69103296T2 (de)	1994-12-01
IL97423A0 (en)	1992-06-21
GB9004857D0 (en)	1990-05-02
EP0446003A1 (fr)	1991-09-11
US5393820A (en)	1995-02-28
DE69103296D1 (de)	1994-09-15
EP0446003B1 (fr)	1994-08-10
WO1991013858A1 (fr)	1991-09-19
DK0446003T3 (da)	1994-10-03

Legal Events

Date	Code	Title
1996-05-14	HP	Change in proprietorship
1997-06-10	KB	Patent renewed
2002-02-10	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
US3760003A (en)	1973-09-18	Halogenated polyphenyl ethers
US6008283A (en)	1999-12-28	Oligomeric flame retardant additive
EP0235266B1 (fr)	1993-03-03	Esters de tetrahalophtalate utilises comme retardateurs de la flamme pour des resines d'ether de polyphenylene
EP0335953A4 (fr)	1990-02-20	Procede de production d'alkylbenzenes superieurs polybromes.
EP0446003B1 (fr)	1994-08-10	Composés ignifuges et compositions les contenant
EP0192885B1 (fr)	1991-03-13	Retardateur de flamme à base d'éthers de bisphénol A halogenés pour les polymères ABS
KR20090127274A (ko)	2009-12-10	스티렌에 사용하기 위한 난연제 조성물
CA1284244C (fr)	1991-05-14	Composition de polymere resistant a l'embrasement
US4546139A (en)	1985-10-08	Polybromo dinaphthyl ethers
EP0073539B1 (fr)	1985-05-15	Composés halogénés et compositions polymères ignifuges dans lesquelles ces composés sont incorporés
US4252967A (en)	1981-02-24	Dihaloneopentyl silicate flame retardants
US5824241A (en)	1998-10-20	Brominated tetrabromophthalate ester flame retardants flame retardant polymer compositions
US3935251A (en)	1976-01-27	2,4,8-Trichloro-tri and tetra bromodibenzofurans
US5043374A (en)	1991-08-27	Halogenated polyester flame retardants for polyphenylene ether, polyolefin and polyethylene terephthalate resins
CA1250310A (fr)	1989-02-21	Esters halogenes sulfures d'alcool neopentylique; preparation et utilisation
JP2673481B2 (ja)	1997-11-05	難燃化合物
CA1333203C (fr)	1994-11-22	Agent ignifuge de type polyester halogene, pour les resines d'ether polyphenylenique
CA1336635C (fr)	1995-08-08	Produits ignifugeants a base d'ester halogenophenylique pour resines de poly(oxyde de phenylene)
JPH08120117A (ja)	1996-05-14	難燃性熱可塑性樹脂組成物
US4299758A (en)	1981-11-10	Halogenated cyclopentadiene diadducts of diacetylenic compounds
US4341692A (en)	1982-07-27	Dihaloneopentyl silicate flame retardants in plastic formulations
CA1218380A (fr)	1987-02-24	SUCCINATE DE BIS(.beta.-PENTABROMOPHENOXYETHYLE), PRODUIT IGNIFUGEANT POUR ABS
Adner et al.	0	Manuscript category
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