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81942

Sigma-Aldrich

Propionic anhydride

purum, ≥96.0% (NT)

Synonym(s):

Propanoic anhydride

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About This Item

Linear Formula:
(CH3CH2CO)2O
CAS Number:
Molecular Weight:
130.14
Beilstein:
507066
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.5 (vs air)

Quality Level

vapor pressure

10 mmHg ( 57.7 °C)

grade

purum

Assay

≥96.0% (NT)

form

liquid

autoignition temp.

545 °F

expl. lim.

11.9 %

refractive index

n20/D 1.404 (lit.)
n20/D 1.404

bp

167 °C (lit.)

mp

−43 °C (lit.)

solubility

H2O: decomposes (when in contact with water)

density

1.010 g/mL at 20 °C
1.015 g/mL at 25 °C (lit.)

functional group

anhydride
ester

SMILES string

CCC(=O)OC(=O)CC

InChI

1S/C6H10O3/c1-3-5(7)9-6(8)4-2/h3-4H2,1-2H3

InChI key

WYVAMUWZEOHJOQ-UHFFFAOYSA-N

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Application

Propionic anhydride can be used:
  • As an esterifying reagent in the modification of cassava starch by acylation reaction.
  • As a reactant along with anisole in the synthesis of 4-methoxypropiophenone using various solid acid catalysts via Friedel−Crafts acylation reaction.
  • As a reagent in the synthesis of cyanohydrin esters by treating KCN with aldehyde in presence of bimetallic titanium(salen) complex catalyst.

Other Notes

Sales restrictions may apply

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

165.2 °F - closed cup

Flash Point(C)

74 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Modification of cassava starch by using propionic anhydride and properties of the starch-blended polyester polyurethane
Santayanon R and Wootthikanokkhan J
Carbohydrate Polymers, 51(1), 17-24 (2003)
Dimensional stabilisation and strength of particleboard by chemical modification with propionic anhydride.
Papadopoulos AN & Gkaraveli A
European Journal of Wood and Wood Products, 61(2), 142-144 (2003)
Synthetic and mechanistic studies on asymmetric cyanohydrin synthesis using a titanium (salen) bimetallic catalyst
Belokon YN, et al.
Tetrahedron, 60(46), 10433-10447 (2004)
Hyung Wook Nam et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 826(1-2), 91-107 (2005-09-17)
N-Terminal isotope tagging (NIT) is an important proteomic tool for quantifying proteins in complex mixtures. Here we describe a modified version of the isotope-coded propionylation procedure of Zhang et al. [Zhang et al., Rapid Commun. Mass Spectom. 16 (2002) 2325]
Robert Meatherall et al.
Journal of analytical toxicology, 33(8), 525-531 (2009-10-31)
Azide in human blood and plasma samples was derivatized with propionic anhydride in a headspace vial without prior sample preparation. The reaction proceeds quickly at room temperature to form propionyl azide. A portion of the headspace was assayed by gas

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