Valeronitrile

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Structural formula
Structural formula of valeronitrile
General
Surname Valeronitrile
other names
  • Pentanoic acid nitrile
  • Butyl cyanide
  • 1-cyanobutane
  • Pentanenitrile
Molecular formula C 5 H 9 N
Brief description

colorless liquid

External identifiers / databases
CAS number 110-59-8
EC number 203-781-8
ECHA InfoCard 100.003.439
PubChem 8061
Wikidata Q27293542
properties
Molar mass 83.1 g mol −1
Physical state

liquid

density

0.80 g cm −3

Melting point

−96 ° C

boiling point

141 ° C

Vapor pressure

7.0 hPa (20 ° C)

solubility

slightly soluble in water (10 g l −1 at 20 ° C)

Refractive index

1.397 (20 ° C)

safety instructions
GHS labeling of hazardous substances
02 - Highly / extremely flammable 07 - Warning

Caution

H and P phrases H: 226-302
P: 210
Toxicological data

332 mg kg −1 ( LD 50ratoral )

As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Valeronitrile is a chemical compound from the group of nitriles .

Extraction and presentation

Valeronitrile 2 can be obtained by heating 1-chlorobutane 1 with sodium cyanide in dimethyl sulfoxide .

Valeronitrile reaction scheme

properties

Valeronitrile is a colorless liquid that is sparingly soluble in water.

use

Valeronitrile can be used to make valeric acid . It can also be used to increase nitrilase activity in many strains of fungi.

safety instructions

The vapors of valeronitrile can form an explosive mixture with air ( flash point 34 ° C, ignition temperature 520 ° C).

Individual evidence

  1. a b c d e f g h i j k Entry on valeronitrile in the GESTIS substance database of the IFA , accessed on December 3, 2018(JavaScript required) .
  2. a b Data sheet Valeronitrile, 99.5% from Sigma-Aldrich , accessed on December 3, 2018 ( PDF ).
  3. Valeronitrile data sheet (PDF) from Merck , accessed on December 3, 2018.
  4. ^ Robert Smiley, Charles Arnold: Notes- Aliphatic Nitriles from Alkyl Chlorides. In: The Journal of Organic Chemistry. 25, 1960, p. 257, doi : 10.1021 / jo01072a600 .