Crotyl alcohol: Difference between revisions
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| UNII_Ref = {{fdacite|correct|FDA}} |
| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = D7F26UNN0B |
| UNII = D7F26UNN0B |
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| EINECS = 207-996-8 |
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| UNNumber = 2614 |
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| ChEBI = 62891 |
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| SMILES = C\C=C\CO |
| SMILES = C\C=C\CO |
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| PubChem = 637922 |
| PubChem = 637922 |
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| BoilingPtC = 121.2 |
| BoilingPtC = 121.2 |
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|Section7={{Chembox Hazards |
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| GHSPictograms = {{GHS02}}{{GHS07}} |
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| GHSSignalWord = Warning |
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| HPhrases = {{H-phrases|226|302|312|315|319}} |
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| PPhrases = {{P-phrases|210|233|240|241|242|243|264|270|280|301+312|302+352|303+361+353|305+351+338|312|321|322|330|332+313|337+313|362|363|370+378|403+235|501}} |
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'''Crotyl alcohol''', or '''crotonyl alcohol''', is an [[Saturated and unsaturated compounds|unsaturated]] [[alcohol]]. It is a colourless liquid that is moderately soluble in water and miscible with most organic solvents. Two isomers of this alcohol exist, cis and trans. |
'''Crotyl alcohol''', or '''crotonyl alcohol''', is an [[Saturated and unsaturated compounds|unsaturated]] [[Alcohols|alcohol]]. It is a colourless liquid that is moderately soluble in water and miscible with most organic solvents. Two isomers of this alcohol exist, cis and trans. |
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It can be synthesized by the [[hydrogenation]] of [[crotonaldehyde]]. The compound is of little commercial interest.<ref name="Ullmann">{{Ullmann | first1 = Jürgen | last1 = Falbe | first2 = Helmut | last2 = Bahrmann | first3 = Wolfgang | last3 = Lipps | first4 = Dieter | last4 = Mayer | title = Alcohols, Aliphatic | doi = 10.1002/14356007.a01_279}}.</ref> |
It can be synthesized by the [[hydrogenation]] of [[crotonaldehyde]]. The compound is of little commercial interest.<ref name="Ullmann">{{Ullmann | first1 = Jürgen | last1 = Falbe | first2 = Helmut | last2 = Bahrmann | first3 = Wolfgang | last3 = Lipps | first4 = Dieter | last4 = Mayer | title = Alcohols, Aliphatic | doi = 10.1002/14356007.a01_279}}.</ref> |
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==See also== |
==See also== |
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*[[Crotyl]] |
*[[Crotyl]] |
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* |
*[[Allyl alcohol]] |
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* |
*[[Crotonaldehyde]] |
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* |
*[[Crotonic acid]] |
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==References== |
==References== |
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Latest revision as of 13:12, 24 July 2024
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| Names | |
|---|---|
| Preferred IUPAC name
(2E)-But-2-en-1-ol | |
| Other names
(E)-But-2-en-1-ol
Crotyl alcohol Crotonyl alcohol 2-Butenol | |
| Identifiers | |
3D model (JSmol)
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|
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.025.533 |
| EC Number |
|
PubChem CID
|
|
| UNII | |
| UN number | 2614 |
CompTox Dashboard (EPA)
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|
| |
| |
| Properties | |
| C4H8O | |
| Molar mass | 72.10 g/mol |
| Density | 0.8454 g/cm3 |
| Melting point | < 25 °C (77 °F; 298 K) |
| Boiling point | 121.2 °C (250.2 °F; 394.3 K) |
| Hazards | |
| GHS labelling: | |
 
| |
| Warning | |
| H226, H302, H312, H315, H319 | |
| P210, P233, P240, P241, P242, P243, P264, P270, P280, P301+P312, P302+P352, P303+P361+P353, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P370+P378, P403+P235, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Crotyl alcohol, or crotonyl alcohol, is an unsaturated alcohol. It is a colourless liquid that is moderately soluble in water and miscible with most organic solvents. Two isomers of this alcohol exist, cis and trans.
It can be synthesized by the hydrogenation of crotonaldehyde. The compound is of little commercial interest.[2]
See also
[edit]References
[edit]- ^ Merck Index, 11th Edition, 2604
- ^ Falbe, Jürgen; Bahrmann, Helmut; Lipps, Wolfgang; Mayer, Dieter. "Alcohols, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_279. ISBN 978-3527306732..
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