Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

177652

Sigma-Aldrich

1,2-Butanediol

98%

Synonym(s):

1,2-Butylene glycol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3CH2CH(OH)CH2OH
CAS Number:
584-03-2
Molecular Weight:
90.12
Beilstein:
969169
EC Number:
209-527-2
MDL number:
MFCD00004570
UNSPSC Code:
12352100
PubChem Substance ID:
24850375
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.438 (lit.)

bp

191-192 °C/747 mmHg (lit.)

density

1.006 g/mL at 25 °C (lit.)

SMILES string

CCC(O)CO

InChI

1S/C4H10O2/c1-2-4(6)3-5/h4-6H,2-3H2,1H3

InChI key

BMRWNKZVCUKKSR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

1,2-Butanediol was used in the synthesis of (R)-2-hydroxybutyric acid.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

200.1 °F - closed cup

Flash Point(C)

93.4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Martin Chaumont et al.
American journal of physiology. Lung cellular and molecular physiology, 316(5), L705-L719 (2019-02-07)
When heated by an electronic cigarette, propylene glycol and glycerol produce a nicotine-carrying-aerosol. This hygroscopic/hyperosmolar aerosol can deposit deep within the lung. Whether these deposits trigger local inflammation and disturb pulmonary gas exchanges is not known. The aim of this
Chao Gao et al.
Bioresource technology, 115, 75-78 (2011-12-01)
(R)-2-Hydroxybutyric acid ((R)-2-HBA) is an important building block for azinothricin family of antitumour antibiotics and biodegradable poly(2-hydroxybutyric acid). However, optically active (R)-2-HBA could not be produced through microbial fermentation or chemical synthesis. Several biocatalytic methods have been reported for the
Joshua Buse et al.
Clinical biochemistry, 73, 98-104 (2019-08-20)
Here we validate a GC, Flame Ionization Detection (GC-FID), liquid injection method using hydrogen as a carrier gas combining analysis of toxic volatile alcohols (VA): methanol, ethanol, isopropanol, acetone, as well as glycols, ethylene glycol (EG) and propylene glycol (PG)
Baokun Tang et al.
Journal of chromatographic science, 53(5), 836-840 (2014-09-18)
Three flavones (quercetin, myricetin and amentoflavone) were extracted from Chamaecyparis obtusa leaves using deep eutectic solvents (DESs) as additives to conventional extractions solvents. Sixteen DESs were synthesized from different salts and hydrogen bond donors. In addition, C. obtusa was extracted
Laurent Imbert et al.
Journal of analytical toxicology, 38(9), 676-680 (2014-09-05)
A liquid chromatography coupled with electrospray tandem mass spectrometry method was developed for the analysis of ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 1,2-butanediol, 2,3-butanediol, 1,2-propanediol and 1,3-propanediol, in serum after a Schotten-Baumann derivatization by benzoyl chloride. Usual validation parameters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service