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Merck
CN

B84807

Sigma-Aldrich

1,4-丁二醇

99%

别名:

1,4-二羟基丁烷, 丁撑二醇

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About This Item

线性分子式:
HO(CH2)4OH
CAS号:
分子量:
90.12
Beilstein:
1633445
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

蒸汽密度

3.1 (vs air)

方案

99%

表单

liquid

自燃温度

698 °F

折射率

n20/D 1.445 (lit.)

沸点

230 °C (lit.)

mp

16 °C (lit.)

密度

1.017 g/mL at 25 °C (lit.)

SMILES字符串

OCCCCO

InChI

1S/C4H10O2/c5-3-1-2-4-6/h5-6H,1-4H2

InChI key

WERYXYBDKMZEQL-UHFFFAOYSA-N

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Anders Hamberg et al.
Chemical communications (Cambridge, England), 48(80), 10013-10015 (2012-09-05)
The enzyme Candida antarctica lipase B was subjected to site directed mutagenesis suggested by molecular modelling. The selectivity for the enzyme increased towards a range of diols over their corresponding monoesters as an effect of the mutations.
Sandra Rinne Dahl et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 885-886, 37-42 (2012-01-10)
The demand of high throughput methods for the determination of gamma-hydroxybutyrate (GHB) and its precursors gamma-butyrolactone (GBL) and 1,4-butane-diol (1,4BD) as well as for pregabalin is increasing. Here we present two analytical methods using ultra-high pressure liquid chromatography (UPLC) and
Harry Yim et al.
Nature chemical biology, 7(7), 445-452 (2011-05-24)
1,4-Butanediol (BDO) is an important commodity chemical used to manufacture over 2.5 million tons annually of valuable polymers, and it is currently produced exclusively through feedstocks derived from oil and natural gas. Herein we report what are to our knowledge
Ari Karchin et al.
Acta biomaterialia, 7(9), 3277-3284 (2011-06-07)
Electrospinning from a melt, in contrast to from a solution, is an attractive tissue engineering scaffold manufacturing process as it allows for the formation of small diameter fibers while eliminating potentially cytotoxic solvents. Despite this, there is a dearth of
An-Ping Zeng et al.
Current opinion in biotechnology, 22(6), 749-757 (2011-06-08)
Diols are chemicals with two hydroxyl groups which have a wide range of appealing applications as chemicals and fuels. In particular, four diol compounds, namely 1,3-propanediol (1,3-PDO), 1,2-propanediol (1,2-PDO), 2,3-butanediol (2,3-BDO) and 1,4-butanediol (1,4-BDO) can be biotechnologically produced by direct

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