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Key Documents

8.00608

Sigma-Aldrich

Propionic anhydride

for synthesis

Synonym(s):

Propionic anhydride

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About This Item

Empirical Formula (Hill Notation):
C6H10O3
CAS Number:
Molecular Weight:
130.14
MDL number:
UNSPSC Code:
12352106
EC Index Number:
204-638-2
NACRES:
NA.22

vapor pressure

1 hPa ( 20 °C)

Quality Level

assay

≥98.0% (GC)

form

liquid

autoignition temp.

285 °C

potency

2360 mg/kg LD50, oral (Rat)
10000 mg/kg LD50, skin (Rabbit)

expl. lim.

1.3-9.5 % (v/v)

pH

2.5 (20 °C, 100 g/L in H2O, calculated on the free acid)

bp

167 °C/1013 hPa

mp

-45 °C

transition temp

flash point 63 °C

density

1.01 g/cm3 at 20 °C

storage temp.

2-30°C

InChI

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

InChI key

WYVAMUWZEOHJOQ-UHFFFAOYSA-N

Application

<ul>
<li><strong>Trace Amines Quantification:</strong> Propionic anhydride is used to derivatize the amino and hydroxyl groups for catecholamines and indolesin (de Bruyn et al., 2024).</li>
<li><strong>Asphaltene Oxidation Research:</strong> It is used in the oxidation of asphaltene and in the synthesis of peroxypropionic acid (Zhao et al., 2023).</li>
<li><strong>In Acylation Reactions:</strong> Used in the acylation of 1,2-methylenedioxybenzene (MDB) during the synthesis of 3,4-methylenedioxypropiophenone (MDP1P) and propionic acid.<br /> (Schiaroli et al., 2023).</li>
</ul>

Analysis Note

Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.009 - 1.011
Identity (IR): passes test

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

145.4 °F

flash_point_c

63 °C


Certificates of Analysis (COA)

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