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398039

Sigma-Aldrich

1,2-Propanediol

ACS reagent, ≥99.5%

Synonym(s):

1,2-PDO, Propylene glycol

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About This Item

Linear Formula:
CH3CH(OH)CH2OH
CAS Number:
Molecular Weight:
76.09
Beilstein/REAXYS Number:
1340498
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

vapor density

2.62 (vs air)

vapor pressure

0.08 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

779 °F

expl. lim.

12.5 %

impurities

≤0.0005 meq/g Titr. acid
≤0.2% water

ign. residue

≤0.005%

color

APHA: ≤10

refractive index

n20/D 1.432 (lit.)

bp

187 °C (lit.)

mp

−60 °C (lit.)

density

1.036 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤1 ppm

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, a 1,2-alkanediol is an industrially important chemical. Due to its increasing demand many green methods have been proposed for its synthesis mainly using the inexpensive glycerol as the starting material. It is a raw material for the synthesis of intermediates, building blocks and polymers.

Application

1,2-Propanediol may be used in the following processes:
  • Green synthesis of propylene carbonate.
  • Production of lactic acid by green catalytic oxidation.
  • Propanal generation by catalytic dehydration.

Other Notes

The article number 398039-4X2L will be discontinued. Please order the single bottle 398039-2L which is physically identical with the same exact specifications.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

Eyeshields, Gloves


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Catalytic Dehydration of 1,2-Propanediol into Propanal over Ag-Modified Silica-Alumina.
Sun D, et al.
Chemistry Letters (Jpn), 43(4), 450-452 (2014)
Efficient one-pot production of 1, 2-propanediol and ethylene glycol from microalgae (Chlorococcum sp.) in water.
Miao G, et al.
Green Chemistry, 17(4), 2538-2544 (2015)
One-pot tandem processing of glycerol stream to 1, 2-propanediol with methanol reforming as hydrogen donor reaction.
Vasiliadou ES, et al.
Applied Catalysis. B, Environmental, 163, 258-266 (2015)
Catalytic conversion of ethyl lactate to 1,2-propanediol over CuO.
Zhang S, et al.
Chinese Journal of Chemical Engineering (2015)
Sustainability metrics for a fossil-and renewable-based route for 1, 2-propanediol production: A comparison.
Marinas A, et al.
Catalysis Today, 239, 31-37 (2015)

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