Identification | Back Directory | [Name]
TRANS,CIS-2,6-NONADIEN-1-OL | [CAS]
7786-44-9 | [Synonyms]
FEMA 2780 NONADIENOL-2,6 T2 C6 NONADIENOL Cucumber alcohol 2,6-Nonadien-1-ol nona-2,6-dien-1-ol Nona-2,6-diene-1-ol Violet-leaf alcohol 2,6-NONADIEN-1-OL/AL Cis-2,6-Nonadien-1-OL (E,Z)-2,6-NONADIEN-1-OL (2E,6E)-2,6-Nonadien-1-ol TRANS 2, CIS 6-NONADIENOL TRANS,CIS-2,6-NONADIEN-1-OL TRANS-2,CIS-6-NONADIEN-1-OL 2,6-nonadienol,(E,Z)-2,6-nonadienol TRANS,CIS-2,6-NONADIEN-1-OL USP/EP/BP | [EINECS(EC#)]
232-097-2 | [Molecular Formula]
C9H16O | [MDL Number]
MFCD00014055 | [MOL File]
7786-44-9.mol | [Molecular Weight]
140.22 |
Hazard Information | Back Directory | [Description]
2,6-Nonadien-l-ol has a powerful, green, vegetable odor. May be prepared from naturally occurring 3-hexen-l-ol (leaf alcohol) to yield the natural trans-2-cis form or from synthetic hexenol to yield the trans-2-trans form. | [Chemical Properties]
2,6-Nonadien-1-ol has a powerful, green, vegetable odor. | [Occurrence]
Originally isolated in the oils of violet leaf and violet flowers (hence, the name “violet leaf alcohol”); also in
cucumber, cornmint oil, prickly pear and malt | [Uses]
trans,cis-2,6-Nonadien-1-ol can be used as antimicrobial compositions for personal care products. | [Taste threshold values]
Taste characteristics at 10 ppm: melon, watermelon, violet, mushroom-like with apple and rosy nuances. | [Synthesis]
Prepared from naturally occurring 3-hexen-1-ol (leaf alcohol) to yield the natural trans-2-cis form or from synthetic
hexanol to yield the trans-2-trans form |
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