| Weight | 83.134 g/mol |
|---|---|
| Formula | C5H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
VALERONITRILE (110-59-8)
n-valeronitrile
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- Comparative toxicities of the naturally occurring nitrile 1-cyano-3,4-epithiobutane and the synthetic nitrile n-valeronitrile in rats: differences in target organs, metabolism and toxic mechanisms. (Food and Chemical Toxicology, 1988)
- Facile cyclization of the valeronitrile group bound to a nickel macrocycle (Journal of the American Chemical Society, 1986)
- Thermodynamic properties of binary mixtures involving sulfolane. 1. Excess volumes on mixing sulfolane and propionitrile, butyronitrile, and valeronitrile (Journal of Chemical & Engineering Data, 1982)
- High pressure phase behavior for the binary mixture of valeronitrile, capronitrile and lauronitrile in supercritical carbon dioxide at temperatures from 313.2 to 393.2 K and pressures from 3.9 to 25.7 MPa (Fluid Phase Equilibria, 2011)
- Synthesis of 2-substituted-5-methylpyridines from methylcyclobutanecarbonitrile, valeronitrile and pentenonitrile intermediates (1990)
- Excess enthalpies of mixing sulfolane + acetonitrile, + propionitrile, + butyronitrile, + valeronitrile at 303.16 K (Journal of Chemical & Engineering Data, 1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - n-valeronitrile
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SMILESCCCCC#N
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InChIKeyRFFFKMOABOFIDF-UHFFFAOYSA-N
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