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155098

Sigma-Aldrich

Valeronitrile

99.5%

Sinónimos:

Butyl cyanide, Pentanenitrile

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About This Item

Fórmula lineal:
CH3(CH2)3CN
Número de CAS:
110-59-8
Peso molecular:
83.13
Beilstein/REAXYS Number:
1736706
EC Number:
203-781-8
MDL number:
MFCD00001974
UNSPSC Code:
12352100
eCl@ss:
39031547
PubChem Substance ID:
24849337
NACRES:
NA.22

Quality Level

200

assay

99.5%

form

liquid

refractive index

n20/D 1.397 (lit.)

bp

139-141 °C (lit.)

mp

−96 °C (lit.)

density

0.795 g/mL at 25 °C (lit.)

functional group

nitrile

SMILES string

CCCCC#N

InChI

1S/C5H9N/c1-2-3-4-5-6/h2-4H2,1H3

InChI key

RFFFKMOABOFIDF-UHFFFAOYSA-N

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Application

Valeronitrile was used in the preparation of valeric acid. It was also used to enhance the nitrilase activity in many strains.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

hcodes

H226,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

100.4 °F - closed cup

flash_point_c

38 °C - closed cup

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCBF1232V
1445156V
1447395
1445158
1445156

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Nils Mohmeyer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(3), 863-872 (2004-12-14)
A new powerful class of low-molecular-weight amphiphilic compounds has been synthesized and their structure-property relationships with respect to their gelation ability of organic solvents have been investigated. These compounds are able to gel organic solvents over a broad range of
Ondrej Kaplan et al.
Journal of industrial microbiology & biotechnology, 33(11), 891-896 (2006-08-16)
2-Cyanopyridine proved to act as a powerful nitrilase inducer in Aspergillus niger K10, Fusarium solani O1, Fusarium oxysporum CCF 1414, Fusarium oxysporum CCF 483 and Penicillium multicolor CCF 2244. Valeronitrile also enhanced the nitrilase activity in most of the strains.
Sofie Snipstad et al.
Ultrasound in medicine & biology, 43(11), 2651-2669 (2017-08-07)
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Porous carbon spheres (CSs) have distinct advantages in energy storage and conversion applications. We report the preparation of highly monodisperse N-doped microporous CSs through the carbonization of polystyrene-based polymer spheres and subsequent activation. The N-doped microporous CSs have a remarkably
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Poly(alkyl cyanoacrylate) (PACA) nanoparticles have shown promise as drug carriers both to solid tumors and across the blood-brain barrier. Efficient drug delivery requires both high cellular uptake of the nanoparticles and release of the drug from the nanoparticles. Release of
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