US4663373A
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Compositions stabilized with substituted aminoxy silanes
Assignee: BASF Corp
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Filing: 1986-05-01
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Granted: 1987-05-05
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Expires: 2006-05-01
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 04:26
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.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 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 |