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P51478

Sigma-Aldrich

Propionic anhydride

97%

Synonym(s):

Propanoic anhydride

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About This Item

Linear Formula:
(CH3CH2CO)2O
CAS Number:
123-62-6
Molecular Weight:
130.14
Beilstein:
507066
EC Number:
204-638-2
MDL number:
MFCD00009303
UNSPSC Code:
12352100
PubChem Substance ID:
24898599
NACRES:
NA.22

vapor density

4.5 (vs air)

Quality Level

200

vapor pressure

10 mmHg ( 57.7 °C)

Assay

97%

autoignition temp.

545 °F

expl. lim.

11.9 %

refractive index

n20/D 1.404 (lit.)

bp

167 °C (lit.)

mp

−43 °C (lit.)

solubility

H2O: decomposes (when in contact with water)

density

1.015 g/mL at 25 °C (lit.)

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 acylating agent for the lipase-catalyzed esterification of alcohols. Recent studies indicate that the particle boards manufactured from wood chips modified with propionic anhydride show enhanced dimensional stability.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

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

Certificates of Analysis (COA)

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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)
Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcohols.
Bianchi D, et al.
The Journal of Organic Chemistry, 53(23), 5531-5534 (1988)
Surendra Nimesh et al.
International journal of pharmaceutics, 337(1-2), 265-274 (2007-01-27)
Polyethylenimine (750 kDa) has been derivatized to influence the proton sponge mechanism and hydrophobic-hydrophilic balance. The polymer was acylated using acid anhydrides of varying carbon chain length, followed by cross-linking with PEG-bis-P to form compact nanoparticles. The chemical linkages in
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
J G Guillot et al.
Journal of analytical toxicology, 21(2), 127-133 (1997-03-01)
We present an analytical method for the determination of heroin, free 6-acetylmorphine (6-AM), and free morphine in blood, urine, and vitreous humor. This method is used in postmortem cases where heroin is the suspected cause of death. The analytical protocol
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