240559
1,4-Butanediol
ReagentPlus®, ≥99%
Synonym(s):
1,4-Butylene glycol, Tetramethylene glycol
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About This Item
Recommended Products
vapor density
3.1 (vs air)
Quality Level
product line
ReagentPlus®
Assay
≥99%
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.)
functional group
hydroxyl
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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General description
1,4-Butanediol is an industrial solvent that is mainly used in the preparation of important polymers such as polyurethanes and polybutylene terephthalate (PET).
Application
1,4-Butanediol may be used in the preparation of 3-buten-1-ol and tetrahydrofuran via dehydration. It may also be used as a reducing agent for carbonyl compounds to form the corresponding alcohols via transfer hydrogenation reaction.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
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)
273.2 °F - closed cup
Flash Point(C)
134 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Kinetics and mechanism of tetrahydrofuran synthesis via 1, 4-butanediol dehydration in high-temperature water
The Journal of Organic Chemistry, 71(16), 6229-6239 (2006)
Dehydration of 1,4-butanediol into 3-buten-1-ol catalyzed by ceria.
Catalysis Communications, 5(8), 397-400 (2004)
Reduction of aldehydes and ketones by transfer hydrogenation with 1, 4-butanediol.
Organic Letters, 9(21), 4387-4389 (2007)
New diol processes: 1, 3-propanediol and 1, 4-butanediol
Applied Catalysis A: General, 280(1), 83-88 (2005)
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
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