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76671

Supelco

Propionitril

analytical standard

Synonym(e):

Ethylcyanid

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About This Item

Lineare Formel:
CH3CH2CN
CAS-Nummer:
107-12-0
Molekulargewicht:
55.08
Beilstein:
773680
EG-Nummer:
203-464-4
MDL-Nummer:
MFCD00001948
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329767256
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥99.5% (GC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

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

bp

97 °C (lit.)

mp (Schmelzpunkt)

−93 °C (lit.)

Dichte

0.772 g/mL at 25 °C (lit.)

Anwendung(en)

environmental

Format

neat

SMILES String

CCC#N

InChI

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

InChIKey

FVSKHRXBFJPNKK-UHFFFAOYSA-N

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Anwendung

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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Piktogramme

FlameSkull and crossbones
GHS02,GHS06

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

42.8 °F - closed cup

Flammpunkt (°C)

6 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG2522
BCCC8119
BCBX9202
BCBW7521
BCBQ9329V

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Improved HPLC of triglycerides by special tempering procedures
Frede E
Chromatographia, 21(1), 29-36 (1986)
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
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
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
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