B84807
1,4-Butanediol
99%
Synonym(s):
1,4-Butylene glycol, Tetramethylene glycol
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About This Item
Linear Formula:
HO(CH2)4OH
CAS Number:
Molecular Weight:
90.12
Beilstein/REAXYS Number:
1633445
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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vapor density
3.1 (vs air)
assay
99%
form
liquid
autoignition temp.
698 °F
refractive index
n20/D 1.445 (lit.)
bp
230 °C (lit.)
mp
16 °C (lit.)
density
1.017 g/mL at 25 °C (lit.)
SMILES string
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.
Qin Zhou et al.
Metabolic engineering, 13(6), 777-785 (2011-10-26)
Conversion of 3-hydroxypropionate (3HP) from 1,3-propanediol (PDO) was improved by expressing dehydratase gene (dhaT) and aldehyde dehydrogenase gene (aldD) of Pseudomonas putida KT2442 under the promoter of phaCAB operon from Ralstonia eutropha H16. Expression of these genes in Aeromonas hydrophila
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
Linbo Wu et al.
Biomacromolecules, 13(9), 2973-2981 (2012-07-27)
Novel potentially biobased aliphatic-aromatic copolyesters poly(butylene succinate-co-butylene furandicarboxylate) (PBSFs) in full composition range were successfully synthesized from 2,5-furandicarboxylic acid (FA), succinic acid (SA), and 1,4-butanediol (BDO) via an esterification and polycondensation process using tetrabutyl titanate (TBT) or TBT/La(acac)(3) as catalyst.
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
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