BE662373A - - Google Patents
Info
- Publication number
- BE662373A BE662373A BE662373DA BE662373A BE 662373 A BE662373 A BE 662373A BE 662373D A BE662373D A BE 662373DA BE 662373 A BE662373 A BE 662373A
- Authority
- BE
- Belgium
- Prior art keywords
- phenyl
- butyl
- benzotriazole
- group
- methyl
- Prior art date
Links
- 239000003381 stabilizer Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 239000012964 benzotriazole Substances 0.000 claims description 8
- 239000004793 Polystyrene Substances 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 5
- 229920002223 polystyrene Polymers 0.000 claims description 5
- 230000000087 stabilizing effect Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- -1 benzotriazole compound Chemical class 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000002530 phenolic antioxidant Substances 0.000 claims description 2
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 claims 1
- PFEFOYRSMXVNEL-UHFFFAOYSA-N 2,4,6-tritert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 PFEFOYRSMXVNEL-UHFFFAOYSA-N 0.000 description 4
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 4
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- YGOXSUSKUVELDI-UHFFFAOYSA-N 2,4,6-tris(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=C(O)C(C(C)(C)CC)=C1 YGOXSUSKUVELDI-UHFFFAOYSA-N 0.000 description 1
- VMZVBRIIHDRYGK-UHFFFAOYSA-N 2,6-ditert-butyl-4-[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VMZVBRIIHDRYGK-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- 239000003508 Dilauryl thiodipropionate Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 description 1
- MBGDPSXEGIIUNX-UHFFFAOYSA-N phosphorous acid;tris(2-nonylphenyl) phosphite Chemical compound OP(O)O.CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC MBGDPSXEGIIUNX-UHFFFAOYSA-N 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 238000002834 transmittance Methods 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
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE662373A true BE662373A (it) |
Family
ID=207380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE662373D BE662373A (it) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE662373A (it) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2300114A1 (de) * | 1973-01-03 | 1975-01-16 | Basf Ag | Selbstverloeschende styrolpolymerisate |
-
0
- BE BE662373D patent/BE662373A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2300114A1 (de) * | 1973-01-03 | 1975-01-16 | Basf Ag | Selbstverloeschende styrolpolymerisate |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0323409B1 (en) | Polyolefin compositions stabilized with long chain N,N-dialkylhydroxylamines | |
| EP2716712B1 (en) | Polycarbonate resin composition and molded article | |
| FR2514016A1 (fr) | Composition a base de polyolefines resistantes aux irradiations gamma et instruments medicaux fabriques avec ces compositions | |
| BE1003823A3 (fr) | Nouvelles compositions stabilisantes a base de derives du phosphore. | |
| US3723427A (en) | Hindered tris(meta-hydroxybenzyl)cyanurate antioxidants | |
| US20090264567A1 (en) | Stabilized Cross-Linked Polyolefin Compositions | |
| FR2678616A1 (fr) | Bis-(benzofuranne-2-ones) et leur application a la stabilisation de matieres organiques. | |
| Naskar et al. | Influence of various stabilizers on ageing of dicumyl peroxide-cured polypropylene/ethylene-propylene-diene thermoplastic vulcanizates | |
| FR2705679A1 (fr) | Nouvelles compositions stabilisantes des matières polymères, à base de phosphonites ou phosphites et d'un stabilisant contre l'hydrolyse. | |
| US20220169829A1 (en) | Compositions and methods for protecting organic polymeric materials from the deleterious effects of exposure to uv-c light | |
| FR2494281A1 (fr) | Phosphites cycliques d'alkylidene- ou d'arylidene-2,2'-bis-phenyles et de polyols, et matieres organiques en contenant comme stabilisants | |
| SK278622B6 (en) | Agent for stabilizing polymers and a polymeric mixture containing same | |
| AU726326B2 (en) | Composition for electric cables | |
| CZ305019B6 (cs) | Polyethylenová kompozice mající zlepšenou odolnost proti předčasnému zesítění při vytlačování, způsob výroby zesítěné polyethylenové kompozice, použití polyethylové kompozice a použití inhibitoru předčasného zesítění v polyethylenové kompozici | |
| US3637582A (en) | Hydroxyphenylalkyleneyl isocyanurates | |
| JPH09510485A (ja) | Hdpeの安定化方法 | |
| FR2682392A1 (fr) | Nouvelles compositions pour la stabilisation des matieres polymeres. | |
| BE662373A (it) | ||
| US4444929A (en) | Unsymmetrical phosphite-phenolic isocyanurate stabilizer combinations | |
| DE3124833A1 (de) | "durch pyrrole stabilisierte chlorhaltige thermoplaste" | |
| US3702837A (en) | Hydroxyphenylalkyleneyl isocyanurate synergist combinations | |
| EP0309285A2 (en) | Polypropylene stabilized against oxidative degradation with mixtures of diarylamine derivatives and sterically hindered phenols | |
| US4163006A (en) | Compositions stabilized with polyalkylthiobenzenes | |
| FR2601006A1 (fr) | Benzylhydroxylamines substituees et leur emploi comme stabilisants, compositions comprenant ces substances et procede pour stabiliser avec ces substances des matieres organiques contre les degradations par oxydation, par la chaleur ou par un rayonnement actinique | |
| EP0705870B1 (de) | Stabilisatoren für organische Materialien |