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177652

Sigma-Aldrich

1,2-Butanediol

98%

Synonym(s):

1,2-Butylene glycol

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About This Item

Linear Formula:
CH3CH2CH(OH)CH2OH
CAS Number:
584-03-2
Molecular Weight:
90.12
Beilstein/REAXYS Number:
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

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Application

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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

wgk_germany

WGK 2

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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’.

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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
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(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
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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)
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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

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