trans-2-Hexenal
| Names | |
|---|---|
| Preferred IUPAC name
(2E)-hex-2-enal | |
| Other names
(trans)-2-Hexenal
(2(E))-hexenal 6728-26-3 (E)-Hex-2-enal 3-propylacrolein β-propylacrolein | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.027.072 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C6H10O | |
| Molar mass | 98.14 g/mol |
| Density | 0.841-0.848 g/cm3 |
| Boiling point | 47.00°C @ 17.00 mmHg |
| Vapor pressure | 6.6 mmHg |
| Hazards | |
| GHS labelling:[1] | |
| Danger | |
| H226, H302, H311, H317, H319, H411 | |
| P210, P233, P240, P241, P242, P243, P261, P262, P264, P264+P265, P270, P272, P273, P280, P301+P317, P302+P352, P303+P361+P353, P305+P351+P338, P316, P321, P330, P333+P317, P337+P317, P361+P364, P362+P364, P370+P378, P391, P403+P235, P405, P501 | |
| Related compounds | |
Related alkenals
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(cis)-3-hexenal |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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trans-2-Hexenal is an organic unsaturated aldehyde with a six-carbon chain. This clear, pale yellow liquid has a green, leafy, herbal fruit smell. It occurs naturally in a wide variety of plants, fruits, vegetables, and spices, and appears to be an important mediating and signalling chemical in plant-fungus and plant-insect interactions, such as the symbiosis between acacia ants and Acacias.