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Cosmetic raw materials

Linalool

Name:Linalool
CAS:78-70-6
Purity:99%

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Factory supply Linalool 78-70-6 with low price

Molecular Formula:C10H18O
Molecular Weight:154.252
Appearance/Colour:liquid
Vapor Pressure:0.17 mm Hg ( 25 °C)
Melting Point:25°C
Refractive Index:1.460 - 1.465
Boiling Point:198.5 °C at 760 mmHg
PKA:14.51±0.29(Predicted)
Flash Point:84.9 °C
PSA：20.23000
Density:0.859 g/cm³
LogP:2.66980

78-70-6 Relevant articles

Influence of heterogenization on catalytic behavior of mono- and bimetallic nanoparticles formed in poly(styrene)-block-poly(4-vinylpyridine) micelles

Sulman, Esther M.,Matveeva, Valentina G.,Sulman, Mikhail G.,Demidenko, Galina N.,Valetsky, Pyotr M.,Stein, Barry,Mates, Tom,Bronstein, Lyudmila M.

, p. 150 - 158 (2009)

Influence of heterogenization on catalyt...

EFFECT OF PHASE COMPOSITION OF PALLADIUM-RUTHENIUM MEMBRANE CATALYST ON SELECTIVITY OF DEHYDROLINALOOL HYDROGENATION

Gryaznov, V. M.,Maganyuk, A. P.,Karavanov, A. N.,Naumov, V. A.

, p. 853 - 855 (1984)

Evidence of an equilibrium between selenides and osmium(VIII) reagents and selenoxides and osmium(VI) reagents

Krief, Alain,Destree, Alexandra,Durisotti, Virginie,Moreau, Nicolas,Smal, Caroline,Colaux-Castillo, Catherine

, p. 558 - 559 (2002)

Driving the equilibrium between selenide...

Structure and Properties of Bimetallic Colloids Formed in Polystyrene-block-Poly-4-vinylpyridine Micelles: Catalytic Behavior in Selective Hydrogenation of Dehydrolinalool

Bronstein, Lyudmila M.,Chernyshov, Dmitrii M.,Volkov, Ilya O.,Ezernitskaya, Marina G.,Valetsky, Peter M.,Matveeva, Valentina G.,Sulman, Esther M.

, p. 302 - 314 (2000)

Catalytic properties of palladium and bi...

Method for efficiently preparing enol through selective hydrogenation of alkynol

-

Paragraph 0052-0061, (2021/03/24)

The invention provides a method for effi...

Method for preparing allyl alcohol compound by reduction of propargyl alcohol compound

-

Paragraph 0059-0060, (2021/11/10)

A hydrazide compound is used as a reduci...

Divergent Total Syntheses of Yaequinolone-Related Natural Products by Late-Stage C-H Olefination

Ces, Sabela Vega,Fernández-Ibá?ez, M. ángeles,Jia, Wen-Liang

supporting information, p. 6259 - 6277 (2021/05/29)

Divergent total syntheses of 10 yaequino...

Hydroxypyridine ligand and preparation method and catalytic application thereof (by machine translation)

-

Paragraph 0077-0079, (2020/05/11)

The invention provides a hydroxypyridine...

78-70-6 Process route

: 106-24-1
Geraniol

: 78-70-6
3,7-dimethylocta-1,6-dien-3-ol

: 123-35-3
7-methyl-3-methene-1,6-octadiene

: 13877-91-3,1856-63-9
3,7-Dimethyl-octa-1,3,6-trien

: 555-10-2
beta-phellandrene

: 4221-98-1
(R)-5-isopropyl-2-methylcyclohexa-1,3-diene

: 502-99-8
3,7-dimethyl-1,3,7-octatriene

Conditions

Conditions	Yield
With boron pentasil zeolite; at 220 ℃; for 2h; under 60.006 Torr; Gas phase;

: 763-10-0
geranyl diphosphate

: 78-70-6
3,7-dimethylocta-1,6-dien-3-ol

: 123-35-3
7-methyl-3-methene-1,6-octadiene

: 106-24-1
Geraniol

: 586-62-9,69073-38-7
Terpinolene

: 98-55-5,2438-12-2
terpineol

: 2009-00-9,10408-16-9,15826-80-9,3387-41-5
sabinene

: 563-34-8,2867-05-2,3917-48-4,75715-79-6
α-thujene

: 5989-54-8,555-08-8,8022-90-0,9003-73-0,95327-98-3
(-)-(S)-limonene