| Identification | More | [Name]
trans-2-Hexen-1-ol | [CAS]
928-95-0 | [Synonyms]
2-HEXENOL
FEMA 2562
HEX-2(TRANS)-EN-1-OL
HEXEN-1-OL,TRANS-2-
T2 HEXENOL
TRANS-1-HYDROXY-2-HEXENE
TRANS-2-HEXEN-1-OL
TRANS-2-HEXEN-1-YL ALCOHOL
TRANS-2-HEXENOL
(2E)-2-Hexen-1-ol
(E)-2-Hexen-1-ol
(E)-2-Hexene-1-ol
(E)-2-hexenol
(E)-Hex-2-en-1-ol
(E)-hex-2-enol
2-(E)-hexenol
2-hexen-1-0l
2-Hexen-1-ol, trans-
Hex-2(E)-enol
trans-2-hexen-1-o | [EINECS(EC#)]
213-191-2 | [Molecular Formula]
C6H12O | [MDL Number]
MFCD00002927 | [Molecular Weight]
100.16 | [MOL File]
928-95-0.mol |
| Chemical Properties | Back Directory | [Appearance]
colourless liquid | [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 | [refractive index ]
n20/D 1.438(lit.)
| [Fp ]
130 °F
| [storage temp. ]
Flammables area | [form ]
Liquid | [pka]
14.45±0.10(Predicted) | [color ]
Clear colorless | [Odor]
at 10.00 % in dipropylene glycol. fresh green leafy fruity unripe banana | [Stability:]
Stable. Flammable. Incompatible with strong oxidizing agents, strong acids. | [biological source]
synthetic | [Odor Type]
fruity | [Water Solubility ]
Slightly soluble in water | [BRN ]
1719709 | [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]
928-95-0(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R10:Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
UN 1987 3/PG 3
| [WGK Germany ]
2
| [RTECS ]
MP8390000
| [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29052900 |
| Hazard Information | Back Directory | [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. | [Chemical Properties]
colourless liquid | [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 |
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