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US4663373A Expired / Lapsed US ⏱️ 0.0 years remaining

Compositions stabilized with substituted aminoxy silanes

Assignee: BASF Corp
•
Filing: 1986-05-01
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Granted: 1987-05-05
•
Expires: 2006-05-01
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Abstract

Abstract Substituted aminoxy silane derivatives corresponding to the formula ##STR1## are effective in stabilizing organic materials against oxidative, thermal and actinic degradation, said derivatives being particularly effective as color improvers and process stabilizers in organic materials containing phenolic antioxidants and/or metal salts of fatty acids and/or hindered amine light stabilizers and/or organic phosphorus compounds.

Inventors

  • 👤 Ramanathan Ravichandran
  • 👤 Thomas E. Snead

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 04:47
CPC Classifications
C; C09; C09K; C09K15/00; C09K15/04; C09K15/32; C09K15/328; C08; C08K; C08K5/00; C08K5/54; C08K5/544

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 64 words
A composition of matter comprising an organic material selected from the group consisting of polymers devoid of silicon atoms, naturally occuring and synthetic mineral oils, animal and vegetable fats, oils and waxes and synthetic ester-based oils, fats and waxes subject to oxidative, thermal and actinic degradation stabilized with an effective stabilizing amount of a compound of the formula ##STR3## wherein n is 0-4; and
Claim 2
Dependent Claim 64 words
A composition of matter comprising an organic material selected from the group consisting of polymers devoid of silicon atoms, naturally occuring and synthetic mineral oils, animal and vegetable fats, oils and waxes and synthetic ester-based oils, fats and waxes subject to oxidative, thermal and actinic degradation stabilized with an effective stabilizing amount of a compound of the formula ##STR3## wherein n is 0-4; and
Claim 3
Dependent Claim 42 words
R, R 1 and R 2 are independently hydrogen, alkyl of 1 to 36 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, aralkyl of 7 to 9 carbon atoms or said aralkyl substituted by alkyl of 1 to 36 carbon atoms.
Claim 4
Dependent Claim 42 words
R, R 1 and R 2 are independently hydrogen, alkyl of 1 to 36 carbon atoms, cycloalkyl of 5 to 12 carbon atoms, aralkyl of 7 to 9 carbon atoms or said aralkyl substituted by alkyl of 1 to 36 carbon atoms.
Claim 5
Dependent Claim 30 words
The composition of claim 1, wherein R 1 and R 2 are independently hydrogen, straight-chain or branched alkyl of 1 to 18 carbon atoms, cyclopentyl, cyclohexyl, benzyl, α-methylbenzyl or α,α-dimethylbenzyl.
Claim 6
Dependent Claim 13 words
The composition of claim 2, wherein R 1 and R 2 are benzyl.
Claim 7
Dependent Claim 13 words
The composition of claim 1, wherein R is C 1 -C 18 alkyl.
Claim 8
Dependent Claim 11 words
The composition of claim 2, wherein said compound is trimethyl mono(N,N-dibenzylaminoxy)silane.
Claim 9
Dependent Claim 11 words
The composition of claim 2, wherein said compound is dimethyl di(N,N-dibenzylaminoxy)silane.
Claim 10
Dependent Claim 10 words
The composition of claim 2, wherein said compound is tetra[N,N-diethylaminoxy]silane.
Claim 11
Dependent Claim 13 words
The composition of claim 1, wherein the organic material is a synthetic polymer.
Claim 12
Dependent Claim 15 words
The composition of claim 8, wherein said synthetic polymer is a polyolefin homopolymer or copolymer.
Claim 13
Dependent Claim 16 words
The composition of claim 9 which also contains a metal salt of a higher fatty acid.
Claim 14
Dependent Claim 11 words
The composition of claim 1, which also contains a phenolic antioxidant.
Claim 15
Dependent Claim 11 words
The composition of claim 10 which also contains a phenolic antioxidant.
Claim 16
Dependent Claim 50 words
The composition of claim 11, wherein said 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-hydroxylhydrocinnamate), di-n-octadecyl 3,5-di-tert-butyl-4-hydroxybenzyl-phosphonate, 1,3,5-tris(3,5-di-tert-butyl-4-hydroxy-benzyl)isocyanurate, thiodiethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate), 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl)benzene, 3,6-di-oxaocta-methylene bis(3-methyl-5-tert-butyl-4-hydroxyhydro-cinnamate), 2,6-di-tert-butyl-p-cresol, 2,2'-ethylidene-bis(4,6-di-tert-butylphenol), 1,3,5-tris(2,6-di- methyl-4-tert-butyl-3-hydroxybenzyl)isocyanurate, 1,1,3-tris-(2-methyl-4-hydroxy-5-tert-butylphenyl)butane, 1,3,5-tris-[2-(3,5-di-tert-butyl-4-hydroxyhydro-cinnamoyloxy)-ethyl]-isocyanurate, 3,5-di-(3,5-di-tert-butyl-4-hydroxybenzyl)-mesitol, hexamethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate), 1-(3,5-di-tert-butyl-4-hydroxyanilino)-3,5-di(octylthio)-s-triazine, N,N'-hexamethylene-bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamamide), calcium bis(ethyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate), ethylene bis[3,3-di(3-tert-butyl-4-hydroxyphenyl)butyrate], octyl 3,5-di-tert-butyl-4-hydroxybenzylmercaptoacetate, bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyl)hydrazide, and N,N'-bis[2-(3,5-tert-butyl-4-hydroxyhydroxocinnamoyloxy)ethyl]oxamide.
Claim 17
Dependent Claim 27 words
The composition of claim 13, wherein said phenolic antioxidant is selected from the group consisting of neopentanetetrayl tetrakis(3,5-di-tert-butyl-4-hydroxy hydrocinnamate), n-octadecyl 3,5-di-tert-butyl-4-hydroxy hydrocinnamate, 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene, 1,3,5-tris-(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, 2,6-di-tert-butyl-p-cresol and 2,2'-ethylidene-bis(4,6-di-tert-butylphenol).
Claim 18
Dependent Claim 61 words
A method for stabilizing an organic material selected from the group consisting of polymers devoid of silicon atoms, naturally occuring and synthetic mineral oils, animal and vegetable fats, oils and waxes and synthetic ester-based oils, fats and waxes against oxidative, thermal and actinic degradation which comprises incorporating into said organic material an effective stabilizing amount of a compound of claim 1.

References Cited (Backward Citations)

SU190016A1 Cited
US3318898A Cited
US3296199A Cited
US3379659A Cited
US3441583A Cited
US3448136A Cited
US3808172A Cited
US3823114A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-05-04 1990-11-03 1991-05-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-05-04 1994-11-03 1995-05-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-05-04 1998-11-03 1999-05-05 $7700.00 Window Closed / Lapsed

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