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T8626

Sigma-Aldrich

Glyceryl tributyrate

≥99%

Sinonimo/i:

1,2,3-Tributyrylglycerol, Glycerol tributyrate, Tributyrin

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About This Item

Formula condensata:
(CH3CH2CH2COOCH2)2CHOCOCH2CH2CH3
Numero CAS:
60-01-5
Peso molecolare:
302.36
Beilstein:
1714746
Numero CE:
200-451-5
Numero MDL:
MFCD00009392
Codice UNSPSC:
12352211
ID PubChem:
24900545
NACRES:
NA.25

Saggio

≥99%

Indice di rifrazione

n20/D 1.435 (lit.)

P. eboll.

129-131 °C/0.03 mmHg (lit.)
287-288 °C (lit.)

Densità

1.032 g/mL at 20 °C (lit.)

Tipo di lipide

neutral glycerides

Stringa SMILE

CCCC(=O)OCC(COC(=O)CCC)OC(=O)CCC

InChI

1S/C15H26O6/c1-4-7-13(16)19-10-12(21-15(18)9-6-3)11-20-14(17)8-5-2/h12H,4-11H2,1-3H3
UYXTWWCETRIEDR-UHFFFAOYSA-N

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Applicazioni


  • Study on the digestive characteristics of short-and medium-chain fatty acid structural lipid and its rapid intervention on gut microbes: In vivo and in vitro studies.: This paper investigates the digestive properties of glyceryl tributyrate and its effects on gut microbiota, highlighting its significance in nutritional biochemistry (Liu et al., 2022).

  • Molecular Characterization of Novel Family IV and VIII Esterases from a Compost Metagenomic Library.: The characterization of novel esterases, including those acting on glyceryl tributyrate, underscores their potential in environmental and industrial biochemistry (Park et al., 2021).

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

345.2 °F - closed cup

Punto d’infiammabilità (°C)

174 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Chelsea R Thorn et al.
Journal of controlled release : official journal of the Controlled Release Society, 319, 168-182 (2019-12-28)
In the advent of the post-antibiotic era, new strategies are urgently required to improve the efficacy of antimicrobials and outsmart multi-drug resistant bacteria. Exploiting a basic survival mechanism of bacteria, lipase production, monoolein liquid crystal nanoparticles (MO-LCNPs) were investigated as
Lonneke Onrust et al.
Veterinary research, 51(1), 56-56 (2020-04-21)
Butyrate has been used extensively as a feed additive to improve gut health and to decrease Salmonella colonization in poultry. Salmonella mainly colonizes the ceca so butyrate concentrations should be increased in this gut segment. Discrepancies on the effects of
Marco A R Vinolo et al.
The Journal of nutritional biochemistry, 22(9), 849-855 (2010-12-21)
Short chain fatty acids (SCFAs) are fermentation products of anaerobic bacteria. More than just being an important energy source for intestinal epithelial cells, these compounds are modulators of leukocyte function and potential targets for the development of new drugs. The
Marco Aurélio Ramirez Vinolo et al.
American journal of physiology. Endocrinology and metabolism, 303(2), E272-E282 (2012-05-25)
The aim of this study was to investigate whether treatment with tributyrin (Tb; a butyrate prodrug) results in protection against diet-induced obesity and associated insulin resistance. C57BL/6 male mice fed a standard chow or high-fat diet were treated with Tb
Lu Han et al.
Journal of agricultural and food chemistry, 59(23), 12635-12642 (2011-11-16)
A kind of low-calorie structured lipid (LCSL) was obtained by interesterification of tributyrin (TB) and methyl stearate (St-ME), catalyzed by a commercially immobilized 1,3-specific lipase, Lipozyme RM IM from Rhizomucor miehei . The condition optimization of the process was conducted
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