Tributyrin

Tributyrin Basic information
Product Name:Tributyrin
Synonyms:GLYCEROL TRI-N-BUTYRATE;1,2,3-TRIBUTYRYLGLYCEROL;Glycery tributyrate;2,3-Bis(butyryloxy)propyl butyrate;Butanoicacid,1,2,3-propanetriylester;Butyric acid triester with glycerin;butyricacidtriesterwithglycerin;Butyrin, tri-
CAS:60-01-5
MF:C15H26O6
MW:302.36
EINECS:200-451-5
Product Categories:Functional Materials;Plasticizer;Polyalcohol Ethers, Esters (Plasticizer);60-01-5
Mol File:60-01-5.mol
Tributyrin Structure
Tributyrin Chemical Properties
Melting point -75 °C
Boiling point 305 °C
density 1.0335
FEMA 2223 | (TRI-)BUTYRIN
refractive index n20/D 1.435(lit.)
Fp 345 °F
storage temp. Store at RT.
solubility H2O: insoluble
form Liquid
color Clear colorless to yellow
Odorat 100.00 %. cheese waxy creamy fatty
Odor Typecheesy
Water Solubility Not miscible in water.
Merck 14,9620
JECFA Number922
BRN 1714746
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyUYXTWWCETRIEDR-UHFFFAOYSA-N
LogP2.95
CAS DataBase Reference60-01-5(CAS DataBase Reference)
EPA Substance Registry SystemTributyrin (60-01-5)
Safety Information
Safety Statements 24/25
WGK Germany 1
RTECS ET7350000
TSCA Yes
HS Code 29171900
Hazardous Substances Data60-01-5(Hazardous Substances Data)
MSDS Information
ProviderLanguage
ACROSEnglish
SigmaAldrichEnglish
ALFAEnglish
Tributyrin Usage And Synthesis
DescriptionTributyrin (C15H26O6), also known as butyrin or glyceryl tributyrate, is the triester of glycerin and butyric acid. It is prepared by esterifcation of glycerin with excess butyric acid. Glycerol tributyrate has a characteristic odor and a bitter taste.
Tributyrin is essentially a triacylglyceride (TAG), which is an ester derived from glycerol and 3 fatty acids. Tributyrin requires lipase to release the butyrate attached to the glycerol. Although 1 tributyrin contains 3 butyrate, not all 3 butyrate is guaranteed to be released. This is because lipase is regioselective. It can hydrolyse triacylglycerides at R1 and R3, only R2, or non-specifically. Lipase also has substrate specificity in that the enzyme can differentiate between acyl chains attached to the glycerol and preferentially cleaving certain types. Since tributyrin requires lipase to release its butyrate, there may be competition between tributyrin and other TAGs for lipase.
Chemical PropertiesTributyrin is a colorless, oily liquid with a bitter taste. It is soluble in alcohol and ether and fairly insoluble in water.
Chemical PropertiesGlycerol tributyrate has a characteristic odor and bitter taste.
UsesTributyrin is a stable and rapidly absorbed prodrug of butyric acid which enhances antiproliferative effects of dihydroxycholecalciferol in human colon cancer cells.
UsesTributyrin is a flavoring agent that is the triester of glycerin and butyric acid. it is prepared by esterification of glycerin with excess butyric acid. it is used in the following foods: baked goods; alcoholic beverages; nonalcoholic beverages; fats and oils; frozen dairy des- serts and mixes; gelatins, puddings and fillings; and soft candy. it is also termed butyrin and glyceryl tributyrate.
Production MethodsTributyrin is manufactured via esterification of glycerol with butyric acid.
DefinitionChEBI: A triglyceride obtained by formal acylation of the three hydroxy groups of glycerol by butyric acid.
PreparationPrepared by esterifcation of glycerol with excess butyric acid.
Taste threshold valuesTaste characteristics at 30 ppm: bitter, waxy, fatty, cheese and butter nuances.
General DescriptionTributyrin is a short-chain triacylglycerol that mainly occurs in butter. It shows potent anti-cancer property.
Biochem/physiol ActionsTaste at 30 ppm
Safety ProfilePoison by intravenous route. Low toxicity by ingestion. Questionable carcinogen with experimental tumorigenic data. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS
CarcinogenicityAdministration of sodium butyrate in drinking water potentiates 1,2-dimethylhydrazine- induced colon cancer in rats . In mice, dietary administration of 5% tributyrin for 48 weeks did not lead to an increase in colonic tumor incidence or focal areas of dysplasia as compared to controls . Therefore, it has been suggested that the agent responsible for enhanced tumorigenesis in the rat study was sodium, rather than butyrate.

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