| Identification | Back Directory | [Name]
FARNESAL | [CAS]
19317-11-4 | [Synonyms]
FARNESAL
FARNESONE
Ai3-32959
FARNESAL 95%
Farnesal, Pract.
Einecs 242-957-9
TIMTEC-BB SBB007716
Farnesal (mixed isomers)
2,6,10-Farnesatrien-1-al
farnesal,mixtureofisomers
FARNESAL 85+% MIXTURE OF ISOMERS
10-dodecatrienal,3,7,11-trimethyl-6
6,10-Dodecatrienal,3,7,11-trimethyl-2
3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL
3,7,11-trimethyl-dodeca-2,6,10-trienal
2,6,10-Dodecatrienal, 3,7,11-trimethyl-
Farnesone (Mixture of Isomers, Technical Grade)
Farnesal, mixture of isomers technical, >=85% (NMR) | [EINECS(EC#)]
242-957-9 | [Molecular Formula]
C15H24O | [MDL Number]
MFCD00038089 | [MOL File]
19317-11-4.mol | [Molecular Weight]
220.35 |
| Chemical Properties | Back Directory | [Boiling point ]
126-129 °C3.5 mm Hg(lit.) | [density ]
0.909 g/mL at 25 °C(lit.) | [FEMA ]
4019 | 3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL | [refractive index ]
n20/D >1.4920(lit.) | [Fp ]
>230 °F | [storage temp. ]
Amber Vial, Refrigerator | [solubility ]
Chloroform (Sparingly), Methanol (Sparingly) | [form ]
Oil | [color ]
Pale Yellow to Yellow | [Odor]
floral minty | [biological source]
synthetic | [Odor Type]
floral | [JECFA Number]
1228 | [BRN ]
1723427 | [Stability:]
Light Sensitive | [Major Application]
flavors and fragrances | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C15H24O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11-12H,5-6,8,10H2,1-4H3/b14-9+,15-11+ | [InChIKey]
YHRUHBBTQZKMEX-YFVJMOTDSA-N | [SMILES]
[H]C(=O)\C=C(/C)CC\C=C(/C)CC\C=C(/C)C | [LogP]
5.20 | [EPA Substance Registry System]
2,6,10-Dodecatrienal, 3,7,11-trimethyl- (19317-11-4) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
36/37/38 | [Safety Statements ]
26-36 | [WGK Germany ]
2 | [F ]
1-10 | [TSCA ]
TSCA listed | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Occurrence]
Reportedly present in tomato, ginger and cardamom. | [Uses]
Farnesal was used in the synthesis of sesquiterpene nanaimoal. | [Uses]
Farnesone is s useful building block for organic synthesis | [Definition]
ChEBI: Farnesal is a farnesane sesquiterpenoid and an enal. | [Preparation]
Reportedly prepared in a patented process by reaction of farnesol with diethyl ether in the presence of a catalyst. | [Synthesis Reference(s)]
Synthetic Communications, 20, p. 3125, 1990 DOI: 10.1080/00397919008051535 | [General Description]
Farnesal has been reported as specific lipid substrate for aldo-keto reductase 1B10 (AKR1B10). The incubation of farnesol with the protoplast of Botryococcus braunii B race strain leads to the formation of farnesal and 3-hydroxy-2,3-dihydrofarnesal. |
|
| Company Name: |
Energy Chemical
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| Website: |
http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
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| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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