155098
Valeronitrile
99.5%
Sinónimos:
Butyl cyanide, Pentanenitrile
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Fórmula lineal:
CH3(CH2)3CN
Número CAS:
Peso molecular:
83.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39031547
UNSPSC Code:
12352100
EC Number:
203-781-8
MDL number:
Beilstein/REAXYS Number:
1736706
Assay:
99.5%
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
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
Application
Valeronitrile was used in the preparation of valeric acid. It was also used to enhance the nitrilase activity in many strains.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Clase de almacenamiento
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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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
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