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FARNESAL

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FARNESAL Basic information

Product Name:
FARNESAL
Synonyms:
  • 10-dodecatrienal,3,7,11-trimethyl-6
  • 3,7,11-trimethyl-dodeca-2,6,10-trienal
  • 6,10-Dodecatrienal,3,7,11-trimethyl-2
  • farnesal,mixtureofisomers
  • TIMTEC-BB SBB007716
  • FARNESAL
  • FARNESONE
  • 3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL
CAS:
19317-11-4
MF:
C15H24O
MW:
220.35
EINECS:
242-957-9
Mol File:
19317-11-4.mol
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FARNESAL Chemical Properties

Boiling point:
126-129 °C3.5 mm Hg(lit.)
Density 
0.909 g/mL at 25 °C(lit.)
refractive index 
n20/D >1.4920(lit.)
FEMA 
4019 | 3,7,11-TRIMETHYL-2,6,10-DODECATRIENAL
Flash point:
>230 °F
storage temp. 
Amber Vial, Refrigerator
solubility 
Chloroform (Sparingly), Methanol (Sparingly)
form 
Oil
color 
Pale Yellow to Yellow
Odor
floral minty
Odor Type
floral
biological source
synthetic
JECFA Number
1228
BRN 
1723427
Stability:
Light Sensitive
LogP
5.20
EPA Substance Registry System
2,6,10-Dodecatrienal, 3,7,11-trimethyl- (19317-11-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
2
1-10

MSDS

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FARNESAL Usage And Synthesis

Occurrence

Reportedly present in tomato, ginger and cardamom.

Uses

Farnesone is s useful building block for organic synthesis

Uses

Farnesal was used in the synthesis of sesquiterpene nanaimoal.

Preparation

Reportedly prepared in a patented process by reaction of farnesol with diethyl ether in the presence of a catalyst.

Definition

ChEBI: Farnesal is a farnesane sesquiterpenoid and an enal.

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.

FARNESALSupplier

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