Ethyl linalool Property

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)

Safety

Toxicity

Both the acute oral LD₅₀ value in rats and the acute dermal LD₅₀ value in rabbits exceeded 5 g/kg (Moreno, 1975).

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P272Contaminated work clothing should not be allowed out of the workplace.

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

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

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

P333+P313IF SKIN irritation or rash occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

Ethyl linalool Chemical Properties,Usage,Production

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).