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1,2-Propanediol

analytical standard

Synonym(s):

1,2-PDO, Propylene glycol

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About This Item

Linear Formula:
CH3CH(OH)CH2OH
CAS Number:
57-55-6
Molecular Weight:
76.09
Beilstein/REAXYS Number:
1340498
EC Number:
200-338-0
MDL number:
MFCD00064272
UNSPSC Code:
41116107
PubChem Substance ID:
329749683
E Number:
E490
NACRES:
NA.24

grade

analytical standard

Quality Level

100

vapor density

2.62 (vs air)

vapor pressure

0.08 mmHg ( 20 °C)

assay

≥99.7% (GC)

autoignition temp.

779 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

12.5 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.432 (lit.)
n20/D 1.433

bp

187 °C (lit.)

mp

−60 °C (lit.)

density

1.036 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)

format

neat

SMILES string

CC(O)CO

InChI

1S/C3H8O2/c1-3(5)2-4/h3-5H,2H2,1H3

InChI key

DNIAPMSPPWPWGF-UHFFFAOYSA-N

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General description

1,2-Propanediol is a compound found to be chemically similar to ethylene glycol and is widely used in automobile antifreeze, activated charcoal preparations, cosmetics, beverages, ointments, etc. It is used as a diluent for the intravenous preparations of poorly water-soluble drugs.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

Find all available reference materials for compounds listed in 10/2011 here

Application

1,2-Propanediol may be used as an analyte protectant for the gas chromatography-mass spectrometric detection of environmental contaminants in honey, honeybees and pollens. It is also used as an analytical reference standard for the quantification of the analyte in biological fluids using headspace-gas chromatography (HS-GC) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Gloves

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1,3-Propanediol United States Pharmacopeia (USP) Reference Standard

USP

1570483

1,3-Propanediol

Glycerol analytical standard

Supelco

77067

Glycerol

Propylene Glycol meets USP testing specifications

Sigma-Aldrich

P4347

Propylene Glycol

Ethylene glycol butyl ether analytical standard

Supelco

53071

Ethylene glycol butyl ether

Multi-residue analysis of 80 environmental contaminants in honeys, honeybees and pollens by one extraction procedure followed by liquid and gas chromatography coupled with mass spectrometric detection.
Wiest L, et al.
Journal of Chromatography A, 1218(34), 5743-5756 (2011)
R S Rajasenan et al.
Toxicology and applied pharmacology, 135(1), 89-99 (1995-11-01)
Engrafting components of human immune systems in severe combined immunodeficient (SCID) mice has been utilized to investigate the pathogenesis of several human autoimmune diseases and may provide a model for studying idiosyncratic drug toxicity. The purpose of this investigation was
G A Reichard et al.
Diabetes, 35(6), 668-674 (1986-06-01)
Plasma acetone turnover rates were measured with the primed continuous infusion of 2-[14C]acetone in patients with moderate to severe diabetic ketoacidosis. Plasma acetone turnover rates ranged from 1.52 to 15.9 mumol X kg-1 X min-1 (108-1038 mumol X 1.73 m-2
H K Vaddi et al.
Journal of pharmaceutical sciences, 91(7), 1639-1651 (2002-07-13)
The respective alcoholic terpenes carvacrol, linalool, and alpha-terpineol were used at 5% w/v in propylene glycol (PG) to increase the in vitro permeation of haloperidol (HP) through human skin. The possible enhancement mechanism was then elucidated with HP-stratum corneum (SC)
Gai Ling Li et al.
Journal of controlled release : official journal of the Controlled Release Society, 84(1-2), 49-57 (2002-10-26)
To achieve a therapeutical effect of the anti-Parkinson's drug R-apomorphine via iontophoresis delivery, enhancement strategies in vitro were explored using three structurally related enhancers, lauric acid (LA), dodecyltrimethylammonium bromide (DTAB) and Laureth-3 oxyethylene ether (C(12)EO(3)). Human stratum corneum and shed
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