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Merck
모든 사진(2)

주요 문서

155098

Sigma-Aldrich

Valeronitrile

99.5%

동의어(들):

Butyl cyanide, Pentanenitrile

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About This Item

Linear Formula:
CH3(CH2)3CN
CAS Number:
Molecular Weight:
83.13
Beilstein:
1736706
EC Number:
MDL number:
UNSPSC 코드:
12352100
eCl@ss:
39031547
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

99.5%

형태

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.)

작용기

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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애플리케이션

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

픽토그램

FlameExclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

100.4 °F - closed cup

Flash Point (°C)

38 °C - closed cup

개인 보호 장비

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


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

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
M A Wallig et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(2), 149-157 (1988-02-01)
Toxic but sublethal oral doses of 125 mg/kg (1.1 mmol/kg) of the cruciferous nitrile, 1-cyano-3,4-epithiobutane (CEB), or 175 mg/kg (2.1 mmol/kg) of its synthetic saturated analogue, n-valeronitrile (VN), were given by gavage to male CDF (F-344/CrlBr) rats once daily for

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