51782

Supelco

Linalool

analytical standard

Synonym(s):
(±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene, (±)-3,7-Dimethyl-1,6-octadien-3-ol
Linear Formula:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS Number:
Molecular Weight:
154.25
Beilstein/REAXYS Number:
1721488
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

grade

analytical standard

vapor pressure

0.17 mmHg ( 25 °C)

assay

≥99.0% (GC)

form

neat

shelf life

limited shelf life, expiry date on the label

application(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.462 (lit.)

bp

194-197 °C/720 mmHg (lit.)

density

0.87 g/mL at 25 °C (lit.)

Featured Industry

Cleaning Products
Cosmetics
Environmental
Flavors and Fragrances
Food and Beverages
Personal Care

format

neat

storage temp.

2-8°C

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

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General description

Certan Vial
Linalool is a principle monoterpene component present in many essential oils of aromatic species, which possess anti-inflammatory property and hence can be used to cure a variety of ailments, found to be both acute and chronic.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation mark

signalword

Warning

hazcat

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

storage_class_code

10 - Combustible liquids

WGK Germany

WGK 1

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Linalool modifies the nicotinic receptor-ion channel kinetics at the mouse neuromuscular junction
Re.L, et al.
Pharmacological Research, 42(2), 177-181 (2000)
Anti-inflammatory activity of linalool and linalyl acetate constituents of essential oils
Peana.T.A, et al.
Phytomedicine, 9(8), 721-726 (2002)
L Re et al.
Pharmacological research, 42(2), 177-182 (2000-07-11)
Linalool is a monoterpene compound reported to be a major component of essential oils in various aromatic species. Several linalool-producing species are used in traditional medical systems. Among these is Aeolanthus suaveolens G. Dom (Labiatae) which is used as an...
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...
Michiko Miyashita et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 53, 174-179 (2012-12-12)
As malignant neoplasm is a major public health problem, there is a need for the development of a novel modulator that enhances antitumor activity and reduces adverse reactions to antitumor agents. In this study, the effects of some volatile oil...
Protocols
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