| Identification | Back Directory | [Name]
TRANS,CIS-2,6-NONADIEN-1-OL | [CAS]
28069-72-9 | [Synonyms]
RA539400
FEMA 2780
Nonadienol
2,6-Nonadienol
Cucumber alchol
T2 C6 NONADIENOL
2E,6Z-Nonadien-1-ol
(E,Z)-2,6-Nonadienol
Nona-2,6(E,Z)-dienol
(e,z)-6-nonadien-1-ol
(E,Z)-nona-2,6-dienol
6-Nonadien-1-ol,(E,Z)-2
(E,Z)-2,6-NONADIEN-1-OL
trans,cis-2，6-Nonadienol
TRANS 2, CIS 6-NONADIENOL
(2E,6Z)-2,6-Nonadien-1-ol
(2E,6Z)-nona-2,6-dien-1-ol
2,6-Nonadien-1-ol, (2E,6Z)-
TRANS,CIS-2,6-NONADIEN-1-OL
TRANS-2,CIS-6-NONADIEN-1-OL
2-trans-6-cis-Nonadien-1-ol
trans-2,cis-6-Nonadienol,94%
trans-2,cis-6-Nonadienol, 94% 5ML
nonadienol,(E,Z)-2,6-nonadien-1-ol
TRANS-2 CIS-6-NONADIEN-1-OL 95+% FCC
trans,cis-2,6-Nonadien-1-ol | [EINECS(EC#)]
248-816-8 | [Molecular Formula]
C9H16O | [MDL Number]
MFCD00014055 | [MOL File]
28069-72-9.mol | [Molecular Weight]
140.22 |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS LIQUID | [Boiling point ]
96-100 °C(lit.)
| [density ]
0.873 g/mL at 25 °C(lit.)
| [FEMA ]
2780 | [refractive index ]
n20/D 1.468(lit.)
| [Fp ]
203 °F
| [storage temp. ]
0-6°C | [form ]
clear liquid | [pka]
14.41±0.10(Predicted) | [color ]
White to yellow liquid | [Odor]
powerful, vegetable odor | [biological source]
synthetic | [Odor Type]
green | [JECFA Number]
1184 | [Major Application]
flavors and fragrances | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,7-8,10H,2,5-6,9H2,1H3/b4-3-,8-7+ | [InChIKey]
AMXYRHBJZOVHOL-ODYTWBPASA-N | [SMILES]
[H]\C(CC)=C(/[H])CC\C([H])=C(/[H])CO | [LogP]
2.71 | [Uses]
Food additive/natural product. | [EPA Substance Registry System]
2,6-Nonadien-1-ol, (2E,6Z)- (28069-72-9) |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS LIQUID | [Hazard]
Low toxicity by ingestion and skin contact.
A skin irritant. | [Definition]
ChEBI: (2E,6Z)-nona-2,6-dien-1-ol is a primary allylic alcohol that is (2E,6Z)-nona-2,6-diene in which a hydrogen at position 1 has been replaced by a hydroxy group. It has a role as a flavouring agent, a plant metabolite and a fragrance. It is an alkenyl alcohol, a volatile organic compound, a primary allylic alcohol and a medium-chain primary fatty alcohol. | [Preparation]
When natural Hexenol is used as a starting material, the preferred isomer will result. This is called "natural" because it is evidently identical to the naturally occurring alcohol. If synthetic Hexenol is used, the less desirable isomer will result. It has a more dry, less pleasant-oily character. There are several methods in use for the production of trans,cis-2,6-Nonadien-1-ol.
| [Synthesis Reference(s)]
Synthesis, p. 528, 1978 DOI: 10.1055/s-1978-24798 |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
jiliang chemicals
|
| Telephone: |
21-62165282 |
| Website: |
http://www.jiliangchem.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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