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240311

Sigma-Aldrich

Propionic anhydride

≥99%

Sinónimos:

Propanoic anhydride

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About This Item

Fórmula lineal:
(CH3CH2CO)2O
Número de CAS:
123-62-6
Peso molecular:
130.14
Beilstein/REAXYS Number:
507066
EC Number:
204-638-2
MDL number:
MFCD00009303
UNSPSC Code:
12352100
PubChem Substance ID:
24854413
NACRES:
NA.22
form:
liquid
assay:
≥99%

vapor density

4.5 (vs air)

Quality Level

200

vapor pressure

10 mmHg ( 57.7 °C)

assay

≥99%

form

liquid

autoignition temp.

545 °F

expl. lim.

11.9 %

refractive index

n20/D 1.404 (lit.)

bp

167 °C (lit.)

mp

−43 °C (lit.)

solubility

chloroform: soluble(lit.)
diethyl ether: soluble(lit.)
ethanol: soluble(lit.)
methanol: soluble(lit.)

density

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 (propanoic anhydride) was used in the preparation of α- and β-1-propionyl derivatives of glucopyranose tetra-acetate.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

165.2 °F - closed cup

flash_point_c

74 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
MKCV3767
MKCV2032
MKCS4636
MKCQ6610
MKCM2117

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F Compernolle et al.
The Biochemical journal, 125(3), 811-819 (1971-12-01)
1. The structures of the alpha(2)- and alpha(3)-azopigments, prepared by diazotization of dog bile with ethyl anthranilate, were shown by mass spectrometry and g.l.c. to correspond to azobilirubin beta-d-xylopyranoside and azobilirubin beta-d-glucopyranoside respectively. 2. Both azopigments consist of a mixture
Mukundan Ragavan et al.
Metabolites, 11(7) (2021-08-07)
Type II diabetes and pre-diabetes are widely prevalent among adults. Elevated serum glucose levels are commonly treated by targeting hepatic gluconeogenesis for downregulation. However, direct measurement of hepatic gluconeogenic capacity is accomplished only via tracer metabolism approaches that rely on
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
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
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]
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