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Merck
CN

76671

Propionitrile

analytical standard

Synonym(s):

Ethyl cyanide

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About This Item

Linear Formula:
CH3CH2CN
CAS Number:
Molecular Weight:
55.08
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
203-464-4
Beilstein/REAXYS Number:
773680
MDL number:
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InChI key

FVSKHRXBFJPNKK-UHFFFAOYSA-N

InChI

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

SMILES string

CCC#N

grade

analytical standard

assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

bp

97 °C (lit.)

mp

−93 °C (lit.)

density

0.772 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

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Application

Propionitrile may be used as a mobile phase for the separation and elution of triglycerides in cocoa butter samples using reversed-phase high-performance liquid chromatography with refractive index detector and temperature programming.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

FlameSkull and crossbones

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

Regulatory Information

监管及禁止进口产品
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Improved HPLC of triglycerides by special tempering procedures
Frede E
Chromatographia, 21(1), 29-36 (1986)
Sung Hee Joo et al.
Environmental science & technology, 41(4), 1288-1296 (2007-06-28)
The decreasing availability of pristine water supplies is prompting drinking water utilities to exploit waters impacted by wastewater effluents and agricultural runoff. As these waters feature elevated organic nitrogen concentrations, the pathways responsible for transformation of organic nitrogen into toxic
Narciso Couto et al.
Rapid communications in mass spectrometry : RCM, 22(4), 582-590 (2008-01-29)
The present work describes a study of the complexation of calcium and magnesium by 3-azidopropionitrile by means of electrospray ionization mass spectrometry (ESI-MS). Complexes were obtained from solutions of calcium and magnesium salts of the type CaX2 and MgX2 (where
David Crich et al.
Carbohydrate research, 341(10), 1467-1475 (2006-04-29)
It is shown that the use of 5% acetonitrile or propionitrile in dichloromethane functions to increase the beta-selectivity of a number of L-rhamnopyranosylation reactions conducted by the thioglycoside method with activation by the 1-benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride couple. The use of
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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