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Tetrahydrolinalool

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Tetrahydrolinalool Basic information

Product Name:
Tetrahydrolinalool
Synonyms:
  • TETRAHYDROLINALOOL
  • (±)-3,7-dimethyl-octan-3-ol
  • 2,6-Dimethyl-6-octanol
  • 3,7-dimethyl-3-octano
  • 3,7-Dimethyloctan-3-ol
  • 3,7-Dimethyloctanol-3
  • Linalool tetrahydride
  • linalooltetrahydride
CAS:
78-69-3
MF:
C10H22O
MW:
158.28
EINECS:
201-133-9
Product Categories:
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Mol File:
78-69-3.mol
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Tetrahydrolinalool Chemical Properties

Melting point:
-1.53°C (estimate)
Boiling point:
71-73 °C/6 mmHg (lit.)
Density 
0.826 g/mL at 25 °C (lit.)
vapor pressure 
11.1Pa at 19.6℃
refractive index 
n20/D 1.434(lit.)
FEMA 
3060 | TETRAHYDROLINALOOL
Flash point:
169 °F
storage temp. 
Sealed in dry,Room Temperature
form 
Liquid
pka
15.34±0.29(Predicted)
Specific Gravity
0.826
color 
Clear colorless
Odor
at 100.00 %. fresh sweet citrus lime floral lily
Odor Type
citrus
Water Solubility 
320mg/L at 25℃
JECFA Number
357
InChIKey
DLHQZZUEERVIGQ-UHFFFAOYSA-N
LogP
3.3 at 20℃
CAS DataBase Reference
78-69-3(CAS DataBase Reference)
NIST Chemistry Reference
3,7-Dimethyl-3-octanol(78-69-3)
EPA Substance Registry System
3-Octanol, 3,7-dimethyl- (78-69-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-36/38
Safety Statements 
26-36-37/39
RIDADR 
NA 1993 / PGIII
WGK Germany 
1
RTECS 
RH0905000
HS Code 
29051990

MSDS

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Tetrahydrolinalool Usage And Synthesis

Chemical Properties

Tetrahydrolinalool is a constituent of honey aroma. It is a colorless liquid with a linalool-like odor that is slightly fresher but distinctly weaker than that of linalool. Tetrahydrolinalool is prepared by catalytic hydrogenation of linalool and is used as a substitute for the less stable linalool in perfuming aggressive media.

Chemical Properties

Tetrahydrolinalool has a sweet, oily, floral odor (more so than linalool) with a citrus floral taste.

Chemical Properties

Clear colorless liquid

Occurrence

Reported found in Virginia tobacco.

Uses

Perfumery, flavoring.

Preparation

By hydrogenation of dl-linalool in the presence of palladium black according to Barbier and Lacquin; also from magnesium ethyl bromide and isoamylketone, or by hydrogenation of 2,6-dimethyl-2-octen-6-ol in the presence of nickel at 100°C; optically active and racemic forms are expected because of the structure of this product.

Definition

ChEBI: A fatty alcohol that is 3-octanol substituted by methyl groups at positions 3 and 7. Metabolite observed in cancer metabolism.

Aroma threshold values

Aroma characteristics at 1%: floral linalool-like with a fatty citrus rind and tea-like nuance.

Taste threshold values

Taste characteristics at 1 to 15 ppm: clean and fresh, floral, tea-like with citrus and herbal nuances.

General Description

The chlorooxidation of 3,7-dimethyl-3-octanol (tetrahydrolinalool) was studied.

Flammability and Explosibility

Non flammable

Tetrahydrolinalool Preparation Products And Raw materials

Raw materials

TetrahydrolinaloolSupplier

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