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ChemicalBook--->CAS DataBase List--->7786-44-9

7786-44-9

7786-44-9 Structure

7786-44-9 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[Boiling point ]

96-100 °C(lit.)
[density ]

0.873 g/mL at 25 °C(lit.)
[FEMA ]

2780 | 2,6-NONADIEN-1-OL
[refractive index ]

n20/D 1.468(lit.)
[Fp ]

203 °F
[pka]

14.67±0.10(Predicted)
[Odor]

at 0.10 % in dipropylene glycol. green cucumber vegetable
[Odor Type]

green
[JECFA Number]

1184
[LogP]

2.71
[EPA Substance Registry System]

2,6-Nonadien-1-ol (7786-44-9)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

38
[Safety Statements ]

26-36-38
[WGK Germany ]

2
[RTECS ]

RA5394000
Hazard InformationBack 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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