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Ethyl linalool

Basic information Safety Supplier Related

Ethyl linalool Basic information

Product Name:
Ethyl linalool
Synonyms:
  • ETHYL LINALOOL
  • 3,7-dimethyl-1,6-nonadien-3-ol
  • 3,7-dimethyl-6-nonadien-3-ol
  • 3,7-dimethylnona-
  • 3,7-dimethylnona-1,6-dien
  • 3,7-dimethylnona-1,6-dien-3-ol
  • 1,6-Nonadien-3-ol, 3,7-dimethyl-
  • 6-NONADIEN-3-OL, 3,7-DIMETHYL-1,85%
CAS:
10339-55-6
MF:
C11H20O
MW:
168.28
EINECS:
233-732-6
Product Categories:
  • Used for synthetic essence and flavor industry
Mol File:
10339-55-6.mol
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Ethyl linalool Chemical Properties

Boiling point:
132℃ (86 Torr)
Density 
0.857±0.06 g/cm3 (20 ºC 760 Torr)
vapor pressure 
18Pa at 25℃
refractive index 
1.4603 (589.3 nm 25℃)
Flash point:
90.9±15.0℃
pka
14.45±0.29(Predicted)
color 
Colourless slightly oily liquid.
Odor
at 100.00 %. fresh bois de rose herbal wet green lavender bergamot
Odor Type
floral
Water Solubility 
656mg/L at 20℃
LogP
3.3
EPA Substance Registry System
1,6-Nonadien-3-ol, 3,7-dimethyl- (10339-55-6)
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Safety Information

Toxicity
Both the acute oral LD50 value in rats and the acute dermal LD50 value in rabbits exceeded 5 g/kg (Moreno, 1975).
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Ethyl linalool Usage And Synthesis

Chemical Properties

Clear colorless to pale yellowish liquid.

Occurrence

Has apparently not been reported to occur in nature.

Uses

Ethyl Linalool is fresh bois de rose herbal wet green lavender bergamot. It has a floral, fresh, bergamot character and is sweeter and less agrestic than Linalool. As with Linalool, it is used in a wide variety of notes for floral bouquets.

Preparation

From methyl ethyl ketone and acetylene through a series of reactions (Bedoukian, 1967).

Metabolism

Tertiary alcohols are not readily metabolized and may be excreted in the urine both unchanged and highly conjugated with glucuronic acid. In rabbits, carbon-carbon double bonds make little difference to the extent of conjugation of terf-hexyl alcohols (Williams, 1959).

Ethyl linalool Preparation Products And Raw materials

Preparation Products

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