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Benzyl cyanide

analytical standard

Synonym(s):

Benzyl nitrile, Phenylacetonitrile

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About This Item

Linear Formula:
C6H5CH2CN
CAS Number:
Molecular Weight:
117.15
Beilstein/REAXYS Number:
385941
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor pressure

0.1 mmHg ( 20 °C)

assay

≥98.0% (GC)

shelf life

limited shelf life, expiry date on the label

refractive index

n20/D 1.520-1.526
n20/D 1.523 (lit.)

bp

233-234 °C (lit.)

mp

−24 °C (lit.)

density

1.015 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

N#CCc1ccccc1

InChI

1S/C8H7N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6H2

InChI key

SUSQOBVLVYHIEX-UHFFFAOYSA-N

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General description

Benzyl cyanide, an aromatic nitrile compound, is widely used as a starting material and as a chemical intermediate in organic chemistry and pharmaceutical applications.

Application

Benzyl cyanide may be used as an analytical standard for the determination of the analyte in fruit samples, frescoes, and desert locusts by gas chromatography (GC) based techniques.

Recommended products

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

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup


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Characterization and medicinal importance of phytoconstituents of C. papaya from down south Indian region using gas chromatography and mass spectroscopy
Upgade A and Bhaskar A
Asian Journal of Pharmaceutical and Clinical Research, 6(4), 101-106 (2013)
Ilaria Bonaduce et al.
Rapid communications in mass spectrometry : RCM, 17(22), 2523-2527 (2003-11-11)
The paper deals with the application of two analytical procedures, based respectively on on-line pyrolysis in the presence of hexamethyldisilazane followed by gas chromatography/mass spectrometric analysis (Py/GC/MS) and on selective extractions and microwave-assisted hydrolysis followed by GC/MS determination. These procedures
R Kermanshai et al.
Phytochemistry, 57(3), 427-435 (2001-06-08)
Papaya (Carica papaya) seeds were extracted in an aqueous buffer or in organic solvents, fractionated by chromatography on silica and aliquots tested for anthelmintic activity by viability assays using Caenorhabditis elegans. For all preparations and fractions tested, anthelmintic activity and

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