BR6244239D0 - PROCESS OF STABILIZATION OF ORGANIC MATERIAL AND THE COMPOSITION OF STABILIZED MATERIAL - Google Patents

PROCESS OF STABILIZATION OF ORGANIC MATERIAL AND THE COMPOSITION OF STABILIZED MATERIAL

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Publication number
BR6244239D0
BR6244239D0 BR14423962A BR14423962A BR6244239D0 BR 6244239 D0 BR6244239 D0 BR 6244239D0 BR 14423962 A BR14423962 A BR 14423962A BR 14423962 A BR14423962 A BR 14423962A BR 6244239 D0 BR6244239 D0 BR 6244239D0
Authority
BR
Brazil
Prior art keywords
tert
butyl
group
alkyl
ethylhexyl
Prior art date
Application number
BR14423962A
Other languages
Portuguese (pt)
Inventor
J Spivack
M Dexter
Original Assignee
Geigy Ag J R
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.)
Filing date
Publication date
Application filed by Geigy Ag J R filed Critical Geigy Ag J R
Publication of BR6244239D0 publication Critical patent/BR6244239D0/en

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Hydrogenated Pyridines (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to amides of the formula: <FORM:0965373/C1/1> in which A is an alkylene or isoalkylene group, R1 is an alkyl group, R2 is hydrogen or an alkyl group, R3 is hydrogen or an alkyl, alkylphenyl or alkylbenzyl group and R4 is an alkyl, alkylphenyl or alkylbenzyl group. Alternatively, R3 and R4, together with the nitrogen atom, may form a morpholino group. The amides are obtainable from the corresponding acids or acid halides and amines, and examples are given of the preparation of N-octadecyl- or N-dodecylphenyl- or N-dodecylbenzyl- or N-tert-octyl-3,5-di-tert-butyl-4-hydroxyphenylacetamide, 3,5-di-tert-butyl-4-hydroxyphenylacetomorpholide, N, N-di-2-ethylhexyl or N,N-di-n-dodecyl 3,5-di-tert-butyl-4-hydroxyphenylacetamide and N-octadecyl b -3,5-di-tert-butyl-4-hydroxyphenyl propionamide. A number of other groups which R1, R2, R3 and R4 may represent are also specified. The products are useful as stabilizers for organic materials liable to oxidative degradation and may be used for stabilizing, inter alia, lubricants and aldehydes. Specified lubricants which may be treated are dihexyl azelate, di-(2-ethylhexyl) azelate, di-(3,5,5-trimethylhexyl) glutarate, di-(3,5,5-trimethylpentyl) glutarate, di-(2-ethylhexyl) pimelate, di-(2-ethylhexyl) adipate, diisoaryl adipate, trianyl tricarbollylate, pentaerythritol tetracaproate, dipropylene glycol dipelargonate and 1,5-pentanediol di-(2-ethylhexanoate). Heptaldehyde is specified as a suitable aldehyde.ALSO:As stabilizers for organic materials liable to oxidative degradation, use is made of amides of the formula: <FORM:0965373/C3/1> in which A is an alkylene or isoalkylene group, R1 is an alkyl group, R2 is hydrogen or an alkyl group, R3 is hydrogen or an alkyl, alkylphenyl or alkylbenzyl group and R4 is an alkyl, alkylphenyl or alkylbenzyl group. Alternatively, R3 and R4, together with the nitrogen atom, may form a morpholino group. Examples are given of the preparation of N-octadecyl- or N-dodecylphenyl-or N-dodecylbenzyl- or N-tert.-octyl- 3,5-ditert.-butyl -4- hydroxyphenylacetamide, 3,5-ditert.-butyl -4- hydroxyphenylacetomorpholide, N, N-di-2-ethylhexyl- or N,N-di-n-dodecyl- 3, 5-di-tert.-butyl -4- hydroxyphenylacetamide and N-octadecyl-b -3, 5-di-tert.-butyl -4- hydroxyphenylpropionamide. A number of other groups which R1, R2, R3 and R4 may represent are also specified. The products may be used for stabilizing polyethylene, polypropylene and polystyrene containing co-polymers of butadiene and styrene. The stabilizers are preferably used in association with dilauryl -b - thiodipropionate or other stabilizer of the general formula: <FORM:0965373/C3/2> where n is 1 or 2 and R7 and R8 are alkyl groups. The compositions of the invention may also contain other antioxidants, pour-point depressants, corrosion and rust inhibitors, dispersing agents, demulsifiers, anti-foaming agents, carbon black, vulcanization accelerators, plasticizers, colour and heat stabilizers, ultraviolet absorbers, dyes, pigments and metal chelating agents. Examples are given of the stabilization of polypropylene and of polystyrene containing butadiene-styrene copolymer.ALSO:As stabilizers for organic materials liable to oxidative degradation, use is made of amides of the formula <FORM:0965373/C4-C5/1> in which A is an alkylene or isoalkylene group, R1 is an alkyl group, R2 is hydrogen or an alkyl group, R3 is hydrogen or an alkyl, alkylphenyl or alkylbenzyl group and R4 is an alkyl, alkylphenyl or alkylbenzyl group. Alternatively, R3 and R4, together with the nitrogen atom, may form a morpholino group. Examples are given of the preparation of N-octadecyl- or N-dodecylphenyl-or N-dodecylbenzyl- or N-tert. - octyl - 3,5 - di - tert. - butyl - 4 - hydroxy-phenylacetamide, 3,5 - di - tert. - butyl - 4 - hydroxyphenylacetomorpholide, N,N - di - 2 - ethylhexyl- or N,N-di-n-dodecyl-3,5-di-tert.-butyl - 4 - hydroxyphenylacetamide and N-octadecyl - b - 3,5 - di - tert. - butyl - 4 - hydroxyphenyl propionamide. A number of other groups which R1, R2, R3 and R4 may represent are also specified. The products may be used for stabilizing lubricants, animal and vegetable oils, hydrocarbon fuels (e.g. gasoline, jet fuel, diesel fuel and fuel oil, waxes, resins and cycloolefines. Specified lubricants which may be treated are dihexyl azelate, di-(2-ethylhexyl)-azelate, di - (3,5,5 - trimethylhexyl) glutarate, di - (3,5,5 - trimethylpentyl) glutarate, di - (2 - ethylhexy) pimelate, di - (2 - ethylhexyl) adipate, diisoamyl adipate, triamyl tricarballylate, pentaerythritol tetracaproate, dipropylene glycol dipelargonate and 1,5-pentanediol di-(2-ethylhexanoate). A number of animal and vegetable oils which may be treated are specified. Cyclohexene is specified as a suitable cyclo-olefine. The stabilizers are preferably used in association with dilauryl-b -thiodipropionate or other stabilizer of the general formula <FORM:0965373/C4-C5/2> where n is 1 or 2 and R7 and R8 are alkyl groups. The compositions of the invention may also contain other antioxidants, pour-point depressants, corrosion and rust inhibitors, dispersing agents, demulsifiers, anti-foaming agents, carbon black, vulcanization accelerators, plasticizers, colour and heat stabilizers, ultraviolet absorbers, dyes, pigments and metal chelating agents. An example is given of the stabilization of a mineral oil.
BR14423962A 1961-10-30 1962-10-29 PROCESS OF STABILIZATION OF ORGANIC MATERIAL AND THE COMPOSITION OF STABILIZED MATERIAL BR6244239D0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US14873961A 1961-10-30 1961-10-30

Publications (1)

Publication Number Publication Date
BR6244239D0 true BR6244239D0 (en) 1973-06-28

Family

ID=22527135

Family Applications (1)

Application Number Title Priority Date Filing Date
BR14423962A BR6244239D0 (en) 1961-10-30 1962-10-29 PROCESS OF STABILIZATION OF ORGANIC MATERIAL AND THE COMPOSITION OF STABILIZED MATERIAL

Country Status (8)

Country Link
BE (1) BE624207A (en)
BR (1) BR6244239D0 (en)
CH (1) CH424244A (en)
DE (1) DE1201350B (en)
FR (1) FR1337164A (en)
GB (1) GB965373A (en)
IT (1) IT954002B (en)
NL (2) NL139019B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1256414B (en) * 1965-08-30 1967-12-14 Union Carbid Australia Ltd Thermoplastic masses for the production of molded articles with resistance to insect attack made of polyethylene or polypropylene
DE2240609A1 (en) * 1972-08-18 1974-02-28 Hoechst Ag METABOLIZING DERIVATIVES OF 4-HYDROXY-3,5-DI-ALKYLPHENYL-PROPIONIC ACID
US4187246A (en) * 1973-09-25 1980-02-05 Ciba-Geigy Corporation Amides of 2,4,6-trialkyl-3-hydroxyphenylalkanoic acids
DE2721398A1 (en) 1976-05-19 1977-12-01 Ciba Geigy Ag ALKYLPHENOL STABILIZERS
US4536346A (en) * 1983-05-06 1985-08-20 American Cyanamid Company Aralkanamidophenyl compounds

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL99615C (en) * 1955-05-18
NL228562A (en) * 1957-06-14 1900-01-01 Geigy Ag J R
NL238332A (en) * 1958-04-21 1900-01-01 Geigy Ag J R

Also Published As

Publication number Publication date
NL139019B (en) 1973-06-15
GB965373A (en) 1964-07-29
BE624207A (en)
IT954002B (en) 1973-08-30
NL284831A (en)
DE1201350B (en) 1965-09-23
FR1337164A (en) 1963-09-06
CH424244A (en) 1966-11-15

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