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2,4-OCTADIEN-1-OL

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2,4-OCTADIEN-1-OL Basic information

Product Name:
2,4-OCTADIEN-1-OL
Synonyms:
  • 2,4-OCTADIEN-1-OL
  • FEMA 3956
  • (2E,4E)-octa-2,4-dienol
  • (E,E)-2,4-Octadien-1-ol
  • 2,4-Octadien-1-ol, (2E,4E)-
  • TRANS-2,TRANS-4-OCTADIENOL
  • trans,trans-2,4-Octadien-1-ol
  • (2E,4E)-2,4-Octadien-1-ol
CAS:
18409-20-6
MF:
C8H14O
MW:
126.2
EINECS:
242-290-3
Product Categories:
  • alcohol Flavor
Mol File:
18409-20-6.mol
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2,4-OCTADIEN-1-OL Chemical Properties

Boiling point:
198℃
Density 
0.868
FEMA 
3956 | (E,E)-2,4-OCTADIEN-1-OL
Flash point:
80℃
pka
14.19±0.10(Predicted)
Odor
at 100.00 %. mild fatty chicken fat creamy waxy
Odor Type
fatty
JECFA Number
1180
LogP
2.30
EPA Substance Registry System
2,4-Octadien-1-ol, (2E,4E)- (18409-20-6)
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Safety Information

HS Code 
2905299090

MSDS

  • Language:English Provider:ALFA
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2,4-OCTADIEN-1-OL Usage And Synthesis

Chemical Properties

(E,E)-2,4-Octadiene-1-ol has a mild, pleasant, fatty odor.

Uses

(2E,4E)-2,4-Octadien-1-ol is a useful intermediate used in the synthesis of sex pheromone component of sphingid moths and other sex attractants.

Definition

ChEBI: (2E,4E)-2,4-octadien-1-ol is an aliphatic alcohol.

Aroma threshold values

Aroma characteristics at 1%: fatty, chicken fat, with a creamy waxy nuance.

Taste threshold values

Taste characteristics at 1 to 5 ppm: fatty, oily and waxy with a broth savory chicken and beef note. Creamy with a cucumber and melon nuance.

Synthesis

64713-73-1

56904-85-9

General method: Diisobutylaluminum hydride (DIBAL-H, 1M hexane solution) was added slowly and dropwise to an anhydrous dichloromethane (DCM) solution of the ester (cas:64713-73-1) at -78°C under argon protection. The reaction mixture was stirred continuously at -78 °C for 1.5 h before the reaction was quenched with 10% aqueous sodium hydroxide (NaOH) solution. Subsequently, the reaction system was gradually warmed to room temperature and stirring was continued for 1 hour. Upon completion of the reaction, the organic and aqueous layers were separated and the aqueous layer was extracted three times with dichloromethane (DCM). All organic phases were combined, washed sequentially with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by fast column chromatography to afford the target product 2,4-octadien-1-ol.

References

[1] Tetrahedron Letters, 2018, vol. 59, # 2, p. 103 - 107

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