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| | trans-2-Hexen-1-ol Basic information |
| | trans-2-Hexen-1-ol Chemical Properties |
| Melting point | 54.63°C | | Boiling point | 158-160 °C(lit.) | | density | 0.849 g/mL at 25 °C(lit.) | | vapor pressure | 1hPa at 20℃ | | FEMA | 2562 | 2-HEXEN-1-OL | | refractive index | n20/D 1.438(lit.) | | Fp | 130 °F | | storage temp. | 2-8°C | | form | Liquid | | pka | 14.45±0.10(Predicted) | | color | Clear colorless | | Odor | at 10.00 % in dipropylene glycol. fresh green leafy fruity unripe banana | | Odor Type | fruity | | Water Solubility | Slightly soluble in water | | BRN | 1719709 | | Stability: | Stable. Flammable. Incompatible with strong oxidizing agents, strong acids. | | LogP | 1.61 at 25℃ | | CAS DataBase Reference | 928-95-0(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Hexen-1-ol, (E)-(928-95-0) | | EPA Substance Registry System | (E)-2-Hexen-1-ol (928-95-0) |
| Hazard Codes | Xi | | Risk Statements | 10-36/37/38 | | Safety Statements | 26-36 | | RIDADR | UN 1987 3/PG 3 | | WGK Germany | 2 | | RTECS | MP8390000 | | TSCA | Yes | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29052900 |
| | trans-2-Hexen-1-ol Usage And Synthesis |
| Chemical Properties | colourless liquid | | Chemical Properties | (E)-2-Hexen-1-ol occurs in many fruits
and has a fruity, green odor, which is sweeter than that of the isomeric (Z)-3-
hexen-1-ol and is, therefore, preferred in aroma compositions. | | Uses | trans-2-Hexen-1-ol was used to evaluate the quality of protected designation of virgin olive oils by headspace solid-phase microextraction-gas chromatography using flame ionization detection and multivariate analysis. It was also used in encapsulation of vanadium catalysts in inorganic and hybrid matrices using sol-gel method. | | Definition | ChEBI: 2-hexen-1-ol is a primary allylic alcohol that is 2-hexene in which a hydrogen at position 1 has been replaced by a hydroxy group. It has a role as a plant metabolite. It is an alkenyl alcohol and a primary allylic alcohol. | | Synthesis Reference(s) | Journal of the American Chemical Society, 93, p. 2792, 1971 DOI: 10.1021/ja00740a040
Tetrahedron Letters, 24, p. 3413, 1983 DOI: 10.1016/S0040-4039(00)86286-3 | | General Description | trans-2-Hexen-1-ol undergoes allylic epoxidation to yield (2R,3R)-(+)-3-propyloxiranemethanol in high pressure carbon dioxide. | | Biochem/physiol Actions | Taste at 2.0-9.0 ppm |
| | trans-2-Hexen-1-ol Preparation Products And Raw materials |
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