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L2602

Linalool

Name: Linalool
Brand: ALDRICH

97%

Synonym(s):

(±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene

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About This Item

Linear Formula:

(CH₃)₂C=CHCH₂CH₂C(CH₃)(OH)CH=CH₂

CAS Number:

78-70-6

Molecular Weight:

154.25

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896318

EC Number:

201-134-4

Beilstein/REAXYS Number:

1721488

MDL number:

MFCD00008906

Assay:

97%

Form:

liquid

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Properties

vapor pressure

0.17 mmHg ( 25 °C)

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.462 (lit.)

bp

194-197 °C/720 mmHg (lit.)

density

0.87 g/mL at 25 °C (lit.)

SMILES string

C\C(C)=C\CCC(C)(O)C=C

InChI

1S/C10H18O/c1-5-10(4,11)8-6-7-9(2)3/h5,7,11H,1,6,8H2,2-4H3

InChI key

CDOSHBSSFJOMGT-UHFFFAOYSA-N

Description

Application

Linalool is generally used as a starting material in the total synthesis of agelasine E analogs and vitamin E derivatives.

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pictograms

GHS07

signalword

Warning

hcodes

H315,H317,H319

pcodes

P261 - P264 - P272 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

171.0 °F - Pensky-Martens closed cup

flash_point_c

77.2 °C - Pensky-Martens closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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A convenient access to (all-rac)-α-tocopherol acetate from linalool and dihydromyrcene

Gembus V, et al.

Bulletin of the Chemical Society of Japan, 82(7), 829-842 (2009)

Synthesis and antimycobacterial activity of agelasine E and analogs.

Bakkestuen AK, et al.

Organic & Biomolecular Chemistry, 3(6), 1025-1033 (2005)

trans-2-Tritylcyclohexanol as a chiral auxiliary in permanganate-mediated oxidative cyclization of 2-methylenehept-5-enoates: application to the synthesis of trans-(+)-linalool oxide.

Ali M Al Hazmi et al.

Organic letters, 16(19), 5104-5107 (2014-09-17)

The permanganate-mediated oxidative cyclization of a series of 2-methylenehept-5-eneoates bearing different chiral auxiliaries was investigated, leading to the discovery of trans-2-tritylcyclohexanol (TTC) as a highly effective chiral controller for the formation of the 2,5-substituted THF diol product with high diastereoselectivity

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Global Trade Item Number

SKU	GTIN
L2602-500G	04061833553763
L2602-100G	04061835361434
L2602-5G	04061835361441