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Merck
CN

V900243

Sigma-Aldrich

1,4-Butanediol

Vetec™, reagent grade, 98%

Synonym(s):

1,4-Butylene glycol, Tetramethylene glycol

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About This Item

Linear Formula:
HO(CH2)4OH
CAS Number:
110-63-4
Molecular Weight:
90.12
Beilstein:
1633445
EC Number:
203-786-5
MDL number:
MFCD00002968
UNSPSC Code:
12352100
PubChem Substance ID:
329829669
Grade:
reagent grade
Assay:
98%
Bp:
230 °C (lit.)

Key Documents

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grade

reagent grade

vapor density

3.1 (vs air)

product line

Vetec™

Assay

98%

autoignition temp.

698 °F

dilution

(for analytical testing)

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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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H336

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD3737V
WXBD0298V
WXBC9657V
MKBK1206V
WXBB1491V

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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.
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
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
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
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