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185590

Sigma-Aldrich

Propionitrile

99%

Sinónimos:

Ethyl cyanide

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About This Item

Fórmula lineal:
CH3CH2CN
Número de CAS:
107-12-0
Peso molecular:
55.08
Beilstein/REAXYS Number:
773680
EC Number:
203-464-4
MDL number:
MFCD00001948
UNSPSC Code:
12352100
PubChem Substance ID:
24851152
NACRES:
NA.22

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.)

SMILES string

CCC#N

InChI

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

InChI key

FVSKHRXBFJPNKK-UHFFFAOYSA-N

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General description

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

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.

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_germany

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

Certificados de análisis (COA)

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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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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