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Merck

155098

Valeronitrile

99.5%

Synonym(s):

Butyl cyanide, Pentanenitrile

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About This Item

Linear Formula:
CH3(CH2)3CN
CAS Number:
110-59-8
Molecular Weight:
83.13
NACRES:
NA.22
PubChem Substance ID:
24849337
eCl@ss:
39031547
UNSPSC Code:
12352100
EC Number:
203-781-8
MDL number:
MFCD00001974
Beilstein/REAXYS Number:
1736706

Product Name

Valeronitrile, 99.5%

InChI key

RFFFKMOABOFIDF-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCC#N

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

Quality Level

200

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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

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBF1232V
1445156V
1447395
1445158
1445156

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Sofie Snipstad et al.
Ultrasound in medicine & biology, 43(11), 2651-2669 (2017-08-07)
Compared with conventional chemotherapy, encapsulation of drugs in nanoparticles can improve efficacy and reduce toxicity. However, delivery of nanoparticles is often insufficient and heterogeneous because of various biological barriers and uneven tumor perfusion. We investigated a unique multifunctional drug delivery
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.
Cheolho Kim et al.
Scientific reports, 7(1), 14400-14400 (2017-11-02)
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
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
Lance M Wheeler et al.
Nature communications, 4, 2197-2197 (2013-07-31)
Colloidal semiconductor nanocrystals have attracted attention for cost-effective, solution-based deposition of quantum-confined thin films for optoelectronics. However, two significant challenges must be addressed before practical nanocrystal-based devices can be realized. The first is coping with the ligands that terminate the
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