trans-2-Hexenal

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)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.027.072
EC Number
  • 229-778-1
KEGG
UNII
  • InChI=1S/C6H10O/c1-2-3-4-5-6-7/h4-6H,2-3H2,1H3/b5-4+
    Key: MBDOYVRWFFCFHM-SNAWJCMRSA-N
  • CCC/C=C/C=O
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
(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

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.