GB361042A - Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids - Google Patents

Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids

Info

Publication number
GB361042A
GB361042A GB2752630A GB2752630A GB361042A GB 361042 A GB361042 A GB 361042A GB 2752630 A GB2752630 A GB 2752630A GB 2752630 A GB2752630 A GB 2752630A GB 361042 A GB361042 A GB 361042A
Authority
GB
United Kingdom
Prior art keywords
acid
salt
ammonium
hydroxy fatty
saponification
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
GB2752630A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB2752630A priority Critical patent/GB361042A/en
Publication of GB361042A publication Critical patent/GB361042A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Salts of a -hydroxy fatty acids such as lactic acid are obtained by treating the reaction product formed by condensing an aldehyde such as acetaldehyde with hydrocyanic acid and saponifying the resulting nitrile by means of a strong inorganic acid, with a base or a compound of a base which forms an insoluble salt with the acid used for the saponification, and a readily soluble salt with the a -hydroxy fatty acid. Suitable salt-forming compounds when sulphuric acid has been used for the saponification are compounds of lead, and when hydrochloric acid has been used, compounds of lead, mercury, or silver are suitable. Examples are given. Specification 300,040, [Class 2 (iii), Dyes &c.], is referred to.ALSO:Salts of a -hydroxy fatty acids, especially calcium and ammonium lactates, are obtained by treating the reaction product formed by condensing an aldehyde such as acetaldehyde with hydrocyanic acid and saponifying the resulting nitrile by means of a strong inorganic acid, with a base or compound of a base which forms an insoluble salt with the acid used for the saponification, and a readily soluble salt with the a -hydroxy fatty acid. Suitable salt-forming compounds when sulphuric acid has been used for the saponification are those of the alkaline-earth metals or lead, and when hydrochloric acid has been used as the saponifiying agent compounds of lead, mercury, or silver are suitable. When lactic acid has been formed by the saponification of its nitrile with sulphuric acid, enough lime may be added to the reaction mixture to form both the soluble calcium lactate, which may subsequently be converted to the ammonium salt, and the insoluble calcium sulphate, which is removed by filtration; or only enough lime to form calcium sulphate may be added, so that the ammonia set free may combine with the lactic acid to form ammonium lactate, which is thus obtained directly. In an alternative method, when the nitrile has been saponified in the presence of an inert diluent in which the ammonium salt of the saponifying acid which is formed is insoluble, according to the method of Specification 300,040, [Class 2 (iii), Dyes &c.], and this ammonium salt has been removed by filtration, the a -hydroxy fatty acid remaining behind may be converted into its ammonium salt by passing gaseous ammonia into the solution. If the saponifying acid has been used in excess, this excess is first precipitated, for example, by adding ammonia or ammonium carbonate, and then filtered off together with the ammonium salt formed by the saponification. Ammonia is led into the solution and the ammonium salt of the a -hydroxy fatty acid formed is precipitated by cooling, if necessary, after distilling off some of the solvent. In one example, in which dioxane is used as the diluent, after filtering off the ammonium lactate formed as above, and evaporating the filtrate a residue of lactic anhydride is left which is converted to ammonium lactate by boiling with milk of lime and subsequent conversion of the calcium lactate formed with ammonium carbonate. Other examples are given.
GB2752630A 1930-09-15 1930-09-15 Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids Expired GB361042A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2752630A GB361042A (en) 1930-09-15 1930-09-15 Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2752630A GB361042A (en) 1930-09-15 1930-09-15 Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids

Publications (1)

Publication Number Publication Date
GB361042A true GB361042A (en) 1931-11-19

Family

ID=10261020

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2752630A Expired GB361042A (en) 1930-09-15 1930-09-15 Improvements in the manufacture and production of lactates and salts of other hydroxy fatty acids

Country Status (1)

Country Link
GB (1) GB361042A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4420636A (en) * 1980-01-04 1983-12-13 Calor Agriculture Research, Inc. Calcium ammonium lactate
WO2008011651A1 (en) * 2006-07-26 2008-01-31 Vtu Holding Gmbh Method for the production of lactic acid or a salt thereof
CN104860812A (en) * 2015-05-20 2015-08-26 北京恩成康泰生物科技有限公司 Preparation method of ammonium lactate solids

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4420636A (en) * 1980-01-04 1983-12-13 Calor Agriculture Research, Inc. Calcium ammonium lactate
WO2008011651A1 (en) * 2006-07-26 2008-01-31 Vtu Holding Gmbh Method for the production of lactic acid or a salt thereof
CN104860812A (en) * 2015-05-20 2015-08-26 北京恩成康泰生物科技有限公司 Preparation method of ammonium lactate solids
CN104860812B (en) * 2015-05-20 2017-07-11 北京恩成康泰生物科技有限公司 A kind of preparation method of ammonium lactate solid

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