GB641443A - Improvements in or relating to the stabilisation of unsaturated ketones - Google Patents

Improvements in or relating to the stabilisation of unsaturated ketones

Info

Publication number
GB641443A
GB641443A GB21285/47A GB2128547A GB641443A GB 641443 A GB641443 A GB 641443A GB 21285/47 A GB21285/47 A GB 21285/47A GB 2128547 A GB2128547 A GB 2128547A GB 641443 A GB641443 A GB 641443A
Authority
GB
United Kingdom
Prior art keywords
ketones
added
ketone
amine
unsaturated
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB21285/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bataafsche Petroleum Maatschappij NV
Original Assignee
Bataafsche Petroleum Maatschappij NV
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 Bataafsche Petroleum Maatschappij NV filed Critical Bataafsche Petroleum Maatschappij NV
Publication of GB641443A publication Critical patent/GB641443A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/86Use of additives, e.g. for stabilisation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Unsaturated ketones which are normally liquid are stabilized against colour change by incorporating therein a minor proportion of a secondary amine. Preferred amines are morpholine and aliphatic mono-amines in which the nitrogen atom is attached to a secondary carbon atom in each of the alkyl groups, e.g. di-sec-butylamine and di-isopropylamine, but many others are specified as suitable; the amount of amine used is normally about 0.01 to 3 per cent by weight. The stabilization is effective even in the presence of iron. The amine may be added to the ketone as such, or added to only a portion thereof and the resulting mixture added to the remaining ketone in an amount sufficient to attain the desired concentration. The pure ketone may be recovered from the stabilized mixture by suitable means, e.g. distillation, fractionation, adsorption and solvent extraction. The process is particularly adapted to ketones having an unsaturated group of at least 3 carbon atoms, such group including an unsaturated tertiary carbon atom, especially when the latter is in the beta position with respect to the carbonyl group. Suitable ketones are listed, both those belonging to these two types and others. Tables are given showing the colour developed in mesityl oxide both with and without a secondary amine as stabilizer.
GB21285/47A 1945-03-13 1947-08-05 Improvements in or relating to the stabilisation of unsaturated ketones Expired GB641443A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US641443XA 1945-03-13 1945-03-13

Publications (1)

Publication Number Publication Date
GB641443A true GB641443A (en) 1950-08-09

Family

ID=22053857

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21285/47A Expired GB641443A (en) 1945-03-13 1947-08-05 Improvements in or relating to the stabilisation of unsaturated ketones

Country Status (1)

Country Link
GB (1) GB641443A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5874631A (en) * 1995-09-23 1999-02-23 Basf Aktiengesellschaft Method and composition to increase the life of Liquid hydroxy-and alkoxyalkyl ketones

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5874631A (en) * 1995-09-23 1999-02-23 Basf Aktiengesellschaft Method and composition to increase the life of Liquid hydroxy-and alkoxyalkyl ketones

Similar Documents

Publication Publication Date Title
GB1062730A (en) Method of purifying ethanolamines
GB641443A (en) Improvements in or relating to the stabilisation of unsaturated ketones
US2151047A (en) Piperidine compound
GB1390851A (en) Antidegradant
GB874570A (en) Thiophosphoric acid esters
GB831448A (en) Stabilized oil extended rubber compositions
US2790014A (en) Stabilized hydrocarbons
GB878118A (en) Process for the stabilisation of chloroprene
GB916137A (en) Stabilization of halogenated aliphatic hydrocarbons
GB1057528A (en) Process for the manufacture of cyanoacetic acid esters
GB997365A (en) Improvements relating to alkyl lead compositions
GB1391716A (en) Colour-stable oxidation inhibitors
GB785869A (en) Improvements in or relating to biocidal compositions
GB666717A (en) A method of isolating lactams
US2617810A (en) Inhibiting oxidation of o-hetero-cyclic compounds
GB708100A (en) Stabilization of acrylonitrile
US3058892A (en) Separation of beta-bromoethylbenzene from alpha-bromoethylbenzene by distillation
US2132018A (en) Inhibition of peroxide formation in ethers
GB835453A (en) Improvements in or relating to stabilized aliphatic chlorohydrocarbons
GB836807A (en) Manufacture of stabilised polyethylene
GB814271A (en) Method for the purification of n,n-dimethylacetamide
GB950899A (en) Improvements in or relating to steroidal alkyl ethers
GB913446A (en) Stabilization of 3,4-dihydro-1,2-pyran-2-carboxaldehyde
ES360631A1 (en) Procedure to improve the vulcanization stability of cis-1,4-polyisoprene. (Machine-translation by Google Translate, not legally binding)
GB868556A (en) Analeptically active ª--hydroxy-and ª--acyloxy-butyric acid alkyl-amides and a process for their manufacture