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US4474914A Expired / Lapsed US ⏱️ 0.0 years remaining

Ortho-alkylated phenyl phosphonites and stabilized organic compositions

Assignee: BASF Corp
•
Filing: 1983-05-31
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Granted: 1984-10-02
•
Expires: 2003-05-31
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Abstract

Abstract Ortho-alkylated phenyl phosphonites of the formula ##STR1## wherein R 1 is alkyl, phenyl or phenyl substituted by alkyl, R 2 is tertiary alkyl or phenylalkyl, and R 3 is hydrogen, alkyl or phenylalkyl are useful as stabilizers for organic polymers and lubricating oils, particularly as processing stabilizers for polyolefins.

Inventors

  • 👤 John d. Spivack

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 08:31
CPC Classifications
C; C07; C07F; C07F9/00; C07F9/02; C07F9/28; C07F9/48; C08; C08K; C08K5/00; C08K5/49; C08K5/51; C08K5/53; C08K5/5393

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 91 words
A composition of matter comprising an organic material subject to oxidative, thermal or actinic degradation stabilized with from 0.01 to 5% weight of a compound of the formula ##STR5## wherein R 1 is alkyl of 1 to 18 carbon atoms, phenyl or phenyl substituted by 1 to 3 alkyl groups with 1 to 8 carbon atoms in each alkyl group, R 2 is tertiary alkyl of 4 to 18 carbon atoms, benzyl, α-methylbenzyl or α,α-dimethylbenzyl, and R 3 is hydrogen, alkyl of 1 to 18 carbon atoms, benzyl, α-methylbenzyl or α,α-dimethylbenzyl.
Claim 2
Dependent Claim 91 words
A composition of matter comprising an organic material subject to oxidative, thermal or actinic degradation stabilized with from 0.01 to 5% weight of a compound of the formula ##STR5## wherein R 1 is alkyl of 1 to 18 carbon atoms, phenyl or phenyl substituted by 1 to 3 alkyl groups with 1 to 8 carbon atoms in each alkyl group, R 2 is tertiary alkyl of 4 to 18 carbon atoms, benzyl, α-methylbenzyl or α,α-dimethylbenzyl, and R 3 is hydrogen, alkyl of 1 to 18 carbon atoms, benzyl, α-methylbenzyl or α,α-dimethylbenzyl.
Claim 3
Dependent Claim 14 words
A composition according to claim 1 wherein the organic material is a synthetic polymer.
Claim 4
Dependent Claim 15 words
A composition according to claim 2 wherein the polymer is a polyolefin homopolymer or copolymer.
Claim 5
Dependent Claim 14 words
A composition according to claim 3 stabilized with O,O'-bis(2,4-di-tert-butylphenyl) phenylphosphonite or 0,0'-bis (2,4-di-tert-octylphenyl) phenylphosphonite.
Claim 6
Dependent Claim 19 words
A composition according to claim 2 which additionally contains from 0.01 to 5% by weight of a phenolic antioxidant.
Claim 7
Dependent Claim 25 words
A composition according to claim 5 wherein the phenolic antioxidant is selected from the group consisting of n-octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate, neopentanetetrayl tetrakis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate), di-n-octadecyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate and 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate.
Claim 8
Dependent Claim 32 words
A composition according to claim 2 which additionally contains from 0.01 to 5% by weight of phenolic antioxidant and from 0.01 to 5% by weight of a UV absorber or light stabilizer.
Claim 9
Dependent Claim 39 words
A composition according to claim 7 wherein the phenolic antioxidant is selected from the group consisting of n-octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate, neopentanetetrayl tetrakis(3,5-di-tert-butyl-4-hydroxyhydroxcnnamate), di-n-octadecyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate and 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate and the UV absorber is selected from the group consisting of 5-chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole and 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole.
Claim 10
Dependent Claim 22 words
A composition according to claim 2 which additionally contains from 0.01 to 5% by weight of a UV absorber or light stabilizer.
Claim 11
Dependent Claim 20 words
A composition according to claim 9 wherein the UV absorber is selected from the group consisting of 5-chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole and 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole.

References Cited (Backward Citations)

US3055861A Cited
US3264324A Cited
US3903208A Cited
US3978020A Cited
US4211731A Cited
US4143028A Cited
US4263230A Cited
US4341880A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-10-02 1988-04-02 1988-10-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-10-02 1992-04-02 1992-10-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-10-02 1996-04-02 1996-10-02 $7700.00 Window Closed / Lapsed

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