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Merck

185590

Propionitrile

99%

Synonym(s):

Ethyl cyanide

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About This Item

Linear Formula:
CH3CH2CN
CAS Number:
107-12-0
Molecular Weight:
55.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851152
EC Number:
203-464-4
Beilstein/REAXYS Number:
773680
MDL number:
MFCD00001948

Key Documents

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Product Name

Propionitrile, 99%

InChI key

FVSKHRXBFJPNKK-UHFFFAOYSA-N

InChI

1S/C3H5N/c1-2-3-4/h2H2,1H3

SMILES string

CCC#N

assay

99%

form

liquid

refractive index

n20/D 1.366 (lit.)

bp

97 °C (lit.)

mp

−93 °C (lit.)

solubility

water: soluble 11.9g/100g at 40 °C
water: soluble 29g/100g at 100 °C
DMF: miscible
alcohol: miscible
diethyl ether: miscible

density

0.772 g/mL at 25 °C (lit.)

functional group

nitrile

Quality Level

200

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Application

Propionitrile was used in mesoporous graphitic C3N4 catalyzed cyclotrimerisation of various nitriles into triazine derivatives. It was used in Raman spectroscopic study of complex formation between o-cresol and propionitrile.

General description

Propionitrile is an experimental duodenal ulcerogen and was found to stimulate gastric acid secretion in the rat.

pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

42.8 °F - closed cup

flash_point_c

6 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH7430
BCCG5203
BCCF4167
BCCF0752
MKCN0887

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S Szabo et al.
Research communications in chemical pathology and pharmacology, 16(2), 311-323 (1977-02-01)
Cysteamine and propionitrile, experimental duodenal ulcerogens, stimulated gastric acid secretion in the rat. Gastric acid secretion was measured by two separate methods, the conventional pylorus ligation technique and a non-invasive technique based on the pH dependent liberation of azure A
A Raman spectroscopic study of complex formation between o-cresol and propionitrile.
Girling RB and Shurvell HF.
Vibrational Spectroscopy, 18(1), 77-82 (1998)
Mesoporous graphitic carbon nitride as a versatile, metal-free catalyst for the cyclisation of functional nitriles and alkynes.
Goettmann F, et al.
New. J. Chem., 31(8), 1455-1460 (2007)
Oliver Kaumanns et al.
The Journal of organic chemistry, 74(1), 75-81 (2008-11-27)
The rates of the reactions of the colored para-substituted phenylacetonitrile anions 1a-c and the phenylpropionitrile anions 2a-c with Michael acceptors (3a-u) were determined by UV-vis spectroscopy in DMSO at 20 degrees C. The reactions follow second-order kinetics, and the corresponding
Atsushi Kunishita et al.
Inorganic chemistry, 47(18), 8222-8232 (2008-08-14)
The copper(II) complexes 1(H) and 1(Ar(X)), supported by the N,N-di(2-pyridylmethyl)benzylamine tridentate ligand (L(H)) or its derivatives having m-substituted phenyl group at the 6-position of pyridine donor groups (L(Ar(X))), have been prepared, and their reactivity toward H2O2 has been examined in
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