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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

Quality Level

200

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

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCM0140
BCCJ9745
BCCL0691
BCCK4057
BCCK4056

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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)
D Somjen et al.
Journal of cellular biochemistry, 112(2), 625-632 (2011-01-27)
In cultured human osteoblasts estradiol-17β (E2) modulated DNA synthesis, the specific activity of creatine kinase BB (CK), 12 and 15 lipoxygenase (LO) mRNA expression and formation of 12- and 15-hydroxyeicosatetraenoic acid (HETE). We now investigate the response of human bone
H V O Carswell et al.
American journal of physiology. Heart and circulatory physiology, 287(4), H1501-H1504 (2004-05-25)
The present study employs selective estrogen receptor (ER) agonists to determine whether 17beta-estradiol-induced neuroprotection in global ischemia is receptor mediated and, if so, which subtype of receptor (ERalpha or ERbeta) is predominantly responsible. Halothane-anesthetized female C57Bl/6J mice were ovariectomized, and
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