2-ethylbutyric acid
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | 2-ethylbutyric acid | ||||||||||||||||||
other names |
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Molecular formula | C 6 H 12 O 2 | ||||||||||||||||||
Brief description |
colorless liquid with a faint odor |
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External identifiers / databases | |||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 116.16 g mol −1 | ||||||||||||||||||
Physical state |
liquid |
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density |
0.92 g cm −3 |
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Melting point |
−31.8 ° C |
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boiling point |
194 ° C |
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Vapor pressure |
0.2 hPa (20 ° C) |
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solubility |
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Refractive index |
1.4130 (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 |
2-Ethylbutyric acid is a chemical compound from the group of carboxylic acids .
Occurrence
2-ethylbutyric acid occurs in tobacco smoke.
Extraction and presentation
2-ethyl butyric acid can be obtained by decarboxylation of diethylmalonic be won.
properties
2-Ethylbutyric acid is a flammable, hardly inflammable, colorless liquid with a faint odor that is sparingly soluble in water.
use
2-Ethylbutyric acid is used as a flavoring and as an intermediate for pharmaceuticals ( e.g. Carbromal ), colorings, esters and other chemicals. It is approved as a feed additive for all animal species.
Individual evidence
- ↑ a b c d e f g h i j k Entry on 2-ethylbutyric acid in the GESTIS substance database of the IFA , accessed on January 31, 2020(JavaScript required) .
- ↑ David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 262 ( limited preview in Google Book search).
- ↑ a b c Data sheet 2-Ethylbutyric acid, 98% from AlfaAesar, accessed on January 31, 2020 ( PDF )(JavaScript required) .
- ↑ Alan Rodgman, Thomas A. Perfetti: The Chemical Components of Tobacco and Tobacco Smoke . CRC Press, 2008, ISBN 978-1-4200-7884-8 , pp. 1536 ( limited preview in Google Book search).
- ^ NL Allinger, et al .: Organic Chemistry. [Main volume] Walter de Gruyter, 2011, ISBN 978-3-11-082970-9 , pp. 1562 ( limited preview in Google Book search).
- ↑ Walter Schunack, Klaus Mayer, Manfred Haake: Drugs textbook of pharmaceutical chemistry . Springer-Verlag, 2013, ISBN 978-3-322-83553-6 , pp. 120 ( limited preview in Google Book search).
- ↑ EUR-Lex: EUR-Lex - 32017R0054 - EN - EUR-Lex , accessed on January 31, 2020