ChemicalBook > CAS DataBase List > TRANS,CIS-2,6-NONADIEN-1-OL

TRANS,CIS-2,6-NONADIEN-1-OL

Product Name
TRANS,CIS-2,6-NONADIEN-1-OL
CAS No.
28069-72-9
Chemical Name
TRANS,CIS-2,6-NONADIEN-1-OL
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
CBNumber
CB9772834
Molecular Formula
C9H16O
Formula Weight
140.22
MOL File
28069-72-9.mol
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TRANS,CIS-2,6-NONADIEN-1-OL Property

Boiling point:
96-100 °C(lit.)
Density 
0.873 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.468(lit.)
FEMA 
2780 | 2,6-NONADIEN-1-OL
Flash point:
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
Odor Type
green
JECFA Number
1184
LogP
2.71
EPA Substance Registry System
2,6-Nonadien-1-ol, (2E,6Z)- (28069-72-9)
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Safety

Hazard Codes 
Xi
Risk Statements 
38
Safety Statements 
26-36-38
WGK Germany 
2
RTECS 
RA5394000
HS Code 
29052990
Toxicity
skn-gpg 100%/24H MOD FCTOD7 20,771,82
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H227Combustible liquid

H315Causes skin irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P370+P378In case of fire: Use … for extinction.

P403+P235Store in a well-ventilated place. Keep cool.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W278009
Product name
trans-2,cis-6-Nonadien-1-ol
Purity
≥95%, stabilized, FCC, FG
Packaging
sample-k
Price
$54.6
Updated
2024/03/01
Sigma-Aldrich
Product number
W278009
Product name
trans-2,cis-6-Nonadien-1-ol
Purity
≥95%,stabilized,FCC,FG
Packaging
100g
Price
$425
Updated
2024/03/01
Sigma-Aldrich
Product number
W278009
Product name
trans-2,cis-6-Nonadien-1-ol
Purity
≥95%,stabilized,FCC,FG
Packaging
1kg
Price
$3320
Updated
2024/03/01
TCI Chemical
Product number
N0593
Product name
trans,cis-2,6-Nonadien-1-ol
Purity
>97.0%(GC)
Packaging
5mL
Price
$90
Updated
2024/03/01
TRC
Product number
N877523
Product name
trans,cis-2,6-Nonadien-1-ol
Packaging
100mg
Price
$60
Updated
2021/12/16
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TRANS,CIS-2,6-NONADIEN-1-OL Chemical Properties,Usage,Production

Chemical Properties

CLEAR COLOURLESS LIQUID

Chemical Properties

(2E,6Z)-2,6-Nonadien-1-ol occurs, for example, in cucumber oil, violet leaf oil, and violet blossom oil. It is a colorless liquid with an intense, heavy, fatty, green odor, reminiscent of violet leaves. The starting material for the synthesis of (2E,6Z)-2,6-nonadien-l-ol is (Z)-3-hexen- 1-ol, which is converted via its halide into the corresponding Grignard reagent. The Grignard reagent is reacted with acrolein to give 1,6-nonadien-3-ol, which is converted into (2E,6Z)-2,6-nonadien-l-ol by allylic rearrangement.
Nonadienal is a powerful fragrance substance. It is used in fine fragrances to create refined violet odors and to impart interesting notes to other blossom compositions. In aroma compositions, it is used for fresh, green cucumber notes.

Uses

trans,cis-2,6-Nonadien-1-ol can be used as antimicrobial compositions for personal care products.

Uses

Food additive/natural product.

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

Hazard

Low toxicity by ingestion and skin contact. A skin irritant.

Safety Profile

Low toxicity by ingestion and skin contact. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.

TRANS,CIS-2,6-NONADIEN-1-OL Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from TRANS,CIS-2,6-NONADIEN-1-OL manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Trans,cis-2,6-nonadien-1-ol 28069-72-9
Price
US $0.00-0.00/Kg
Min. Order
1KG
Purity
99.0%+
Supply Ability
100 tons
Release date
2020-01-16
Career Henan Chemical Co
Product
TRANS,CIS-2,6-NONADIEN-1-OL 28069-72-9
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
JD 590
Release date
2019-09-01
Career Henan Chemical Co
Product
TRANS,CIS-2,6-NONADIEN-1-OL 28069-72-9
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
JD 640
Release date
2019-09-01

28069-72-9, TRANS,CIS-2,6-NONADIEN-1-OLRelated Search:


  • (2E,6Z)-2,6-Nonadien-1-ol
  • (E,Z)-2,6-Nonadienol
  • trans,cis-2,6-Nonadienol
  • trans-2,cis-6-Nonadienol, 94% 5ML
  • Cucumber alchol
  • RA539400
  • trans-2,cis-6-Nonadienol,94%
  • 2E,6Z-Nonadien-1-ol
  • <i>trans</i>,<i>cis</i>-2,6-Nonadien-1-ol
  • FEMA 2780
  • (E,Z)-2,6-NONADIEN-1-OL
  • T2 C6 NONADIENOL
  • TRANS,CIS-2,6-NONADIEN-1-OL
  • TRANS-2,CIS-6-NONADIEN-1-OL
  • TRANS 2, CIS 6-NONADIENOL
  • (e,z)-6-nonadien-1-ol
  • (E,Z)-nona-2,6-dienol
  • 2,6-Nonadienol
  • 2-trans-6-cis-Nonadien-1-ol
  • 6-Nonadien-1-ol,(E,Z)-2
  • Nona-2,6(E,Z)-dienol
  • Nonadienol
  • (2E,6Z)-nona-2,6-dien-1-ol
  • TRANS-2 CIS-6-NONADIEN-1-OL 95+% FCC
  • nonadienol,(E,Z)-2,6-nonadien-1-ol
  • 2,6-Nonadien-1-ol, (2E,6Z)-
  • trans,cis-2,6-Nonadien-1-ol&gt
  • trans,cis-2,6-Nonadien-1-ol, ≥ 97.0%
  • 28069-72-9
  • CH3CH2CHCHCH2CH2CHCHCH2OH
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