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76671

Supelco

Propionitrile

analytical standard

Synonym(s):

Ethyl cyanide

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About This Item

Linear Formula:
CH3CH2CN
CAS Number:
107-12-0
Molecular Weight:
55.08
Beilstein:
773680
EC Number:
203-464-4
MDL number:
MFCD00001948
UNSPSC Code:
41116107
PubChem Substance ID:
329767256
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.366 (lit.)
n20/D 1.366

bp

97 °C (lit.)

mp

−93 °C (lit.)

density

0.772 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

CCC#N

InChI

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

InChI key

FVSKHRXBFJPNKK-UHFFFAOYSA-N

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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.

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Pictograms

FlameSkull and crossbones
GHS02,GHS06

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

42.8 °F - closed cup

Flash Point(C)

6 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL7833
BCCJ3884
BCCG2522
BCCC8119
BCBX9202

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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
Sergey I Druzhinin et al.
The journal of physical chemistry. A, 110(47), 12760-12768 (2006-11-28)
Fast intramolecular charge transfer (ICT) accompanied by dual fluorescence from a locally excited (LE) and an ICT state taking place with N-phenylpyrrole (PP) in the solvent n-propyl cyanide (PrCN) is investigated as a function of temperature between 25 and -112
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
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
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