Valeronitrile
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Valeronitrile | |||||||||||||||
other names |
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Molecular formula | C 5 H 9 N | |||||||||||||||
Brief description |
colorless liquid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 83.1 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
0.80 g cm −3 |
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Melting point |
−96 ° C |
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boiling point |
141 ° C |
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Vapor pressure |
7.0 hPa (20 ° C) |
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solubility |
slightly soluble in water (10 g l −1 at 20 ° C) |
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Refractive index |
1.397 (20 ° C) |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
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 .
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
- ↑ 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) .
- ↑ a b Data sheet Valeronitrile, 99.5% from Sigma-Aldrich , accessed on December 3, 2018 ( PDF ).
- ↑ Valeronitrile data sheet (PDF) from Merck , accessed on December 3, 2018.
- ^ Robert Smiley, Charles Arnold: Notes- Aliphatic Nitriles from Alkyl Chlorides. In: The Journal of Organic Chemistry. 25, 1960, p. 257, doi : 10.1021 / jo01072a600 .