2-ethyl-3-hydroxyhexanal
Structural formula | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
General | ||||||||||||||||
Surname | 2-ethyl-3-hydroxyhexanal | |||||||||||||||
other names |
|
|||||||||||||||
Molecular formula | C 8 H 16 O 2 | |||||||||||||||
External identifiers / databases | ||||||||||||||||
|
||||||||||||||||
properties | ||||||||||||||||
Molar mass | 144.21 g · mol -1 | |||||||||||||||
Physical state |
liquid |
|||||||||||||||
density |
0.9397 g cm −3 (20 ° C ) |
|||||||||||||||
boiling point |
138 ° C |
|||||||||||||||
Refractive index |
1.4409 (20 ° C) |
|||||||||||||||
safety instructions | ||||||||||||||||
|
||||||||||||||||
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-Ethyl-3-hydroxyhexanal (also butyraldol ) is a chemical compound from the group of aldols .
Obtaining, displaying and using
2-Ethyl-3-hydroxyhexanal is industrially synthesized from propene . In a first step, the propene is reacted with a mixture of carbon monoxide and hydrogen in a process known as hydroformylation . This initially results in n- butanal and iso- butanal .
The 2-ethyl-3-hydroxyhexanal is produced in a further step by the aldol addition of two n- butanal molecules in an alkaline solution .
2-Ethyl-3-hydroxyhexanal is an intermediate in industrial synthetic chemistry . 2-Ethylhexanol can be produced by dehydration .
See also
Individual evidence
- ↑ a b H. Panda: Handbook On Chemical Industries (Alcohol Based) . ASIA PACIFIC BUSINESS PRESS Inc., 2002, ISBN 978-81-7833-067-9 , pp. 137 ( limited preview in Google Book search).
- ^ William M. Haynes: CRC Handbook of Chemistry and Physics, 95th Edition . CRC Press, 2014, ISBN 978-1-4822-0868-9 , pp. 260 ( limited preview in Google Book Search).
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ a b Process for the production of 2-ethylhexanol: DE 3530839 A1 , August 29, 1985; EP 0216151 B1 , August 20, 1986.