GB456525A - Manufacture of glycerole mono-lactate - Google Patents
Manufacture of glycerole mono-lactateInfo
- Publication number
- GB456525A GB456525A GB1112335A GB1112335A GB456525A GB 456525 A GB456525 A GB 456525A GB 1112335 A GB1112335 A GB 1112335A GB 1112335 A GB1112335 A GB 1112335A GB 456525 A GB456525 A GB 456525A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzene
- glycerol
- alcohol
- lactate
- monolactate
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/03—Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Glycerol monolactate is made by heating glycerol with a lactic acid ester of an alcohol boiling below 100 DEG C. The reactants in about equimolecular proportions may be heated in the presence of an esterification catalyst, the temperature being kept below 100 DEG C. A solvent or diluent boiling below 100 DEG C. may be present which facilitates removal of the liberated alcohol. In an example, ethyl lactate, glycerol, benzene, and sulphuric acid are boiled together under a fractionating column, the vapours of alcohol and benzene which distil being condensed, washed with water, and the separating benzene continuously returned. After neutralization with caustic soda, benzene is removed by distillation. The glycerol monolactate contains a trace of sodium sulphate. To avoid this, barium hydroxide may be used in neutralizing and the precipitate separated. Methyl lactate may replace the ethyl ester. Specification 346,486 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1112335A GB456525A (en) | 1935-04-10 | 1935-04-10 | Manufacture of glycerole mono-lactate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1112335A GB456525A (en) | 1935-04-10 | 1935-04-10 | Manufacture of glycerole mono-lactate |
Publications (1)
Publication Number | Publication Date |
---|---|
GB456525A true GB456525A (en) | 1936-11-10 |
Family
ID=9980449
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1112335A Expired GB456525A (en) | 1935-04-10 | 1935-04-10 | Manufacture of glycerole mono-lactate |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB456525A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2584998A (en) * | 1948-06-18 | 1952-02-12 | Edward M Filachione | Mixed glycerol esters and their acylation products |
CN102675103A (en) * | 2012-04-27 | 2012-09-19 | 孝感市易生新材料有限公司 | Method for producing menthyl lactate with high content and high optical purity by using two-step method |
-
1935
- 1935-04-10 GB GB1112335A patent/GB456525A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2584998A (en) * | 1948-06-18 | 1952-02-12 | Edward M Filachione | Mixed glycerol esters and their acylation products |
CN102675103A (en) * | 2012-04-27 | 2012-09-19 | 孝感市易生新材料有限公司 | Method for producing menthyl lactate with high content and high optical purity by using two-step method |
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