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Merck
CN

73105

三丁酸甘油酯

analytical standard

别名:

丁酸-1,2,3-三丙酯, 三丁精, 三丁酸甘油酯

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关于此项目

线性分子式:
(CH3CH2CH2COOCH2)2CHOCOCH2CH2CH3
化学文摘社编号:
60-01-5
分子量:
302.36
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329764615
EC Number:
200-451-5
Beilstein/REAXYS Number:
1714746
MDL number:
MFCD00009392

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产品名称

三丁酸甘油酯, analytical standard

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

InChI key

UYXTWWCETRIEDR-UHFFFAOYSA-N

SMILES string

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

grade

analytical standard

assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.434-1.436
n20/D 1.435 (lit.)

bp

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

density

1.032 g/mL at 20 °C (lit.)

application(s)

food and beverages

format

neat

Quality Level

100

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相关类别

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存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

345.2 °F - closed cup

flash_point_c

174 °C - closed cup

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCM4541
BCCM4982
BCCJ1265
BCCB7782
BCBS8233V

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Gail A Cresci et al.
Alcoholism, clinical and experimental research, 38(6), 1489-1501 (2014-06-04)
Excessive alcohol consumption leads to liver disease. Interorgan crosstalk contributes to ethanol (EtOH)-induced liver injury. EtOH exposure causes gut dysbiosis resulting in negative alterations in intestinal fermentation byproducts, particularly decreased luminal butyrate concentrations. Therefore, in the present work, we investigated
Soon-Seok Hong et al.
International journal of pharmaceutics, 483(1-2), 142-150 (2015-02-11)
A high drug-loading capacity is a critical factor for the clinical development of liposomal formulations. The accommodation of hydrophobic drugs within the liposomal membrane is often limited in saturated phosphatidylcholine (PC)-based liposomes owing to the rigidity of the lipid acyl
Mette U Anby et al.
Molecular pharmaceutics, 11(11), 4069-4083 (2014-09-30)
The impact of gastrointestinal (GI) processing and first pass metabolism on danazol oral bioavailability (BA) was evaluated after administration of self-emulsifying drug delivery systems (SEDDS) in the rat. Danazol absolute BA was determined following oral and intraduodenal (ID) administration of

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