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L2602

Sigma-Aldrich

Linalool

97%

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Synonym(s):
(±)-3,7-Dimethyl-1,6-octadien-3-ol, (±)-3,7-Dimethyl-3-hydroxy-1,6-octadiene
Linear Formula:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS Number:
Molecular Weight:
154.25
Beilstein:
1721488
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

0.17 mmHg ( 25 °C)

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

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This Item
61706PHL808858.18627
Linalool 97%

Sigma-Aldrich

L2602

Linalool

Linalool certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

61706

Linalool

Linalool phyproof® Reference Substance

PHL80885

Linalool

Linalool for synthesis

Sigma-Aldrich

8.18627

Linalool

form

liquid

form

-

form

liquid

form

liquid

refractive index

n20/D 1.462 (lit.)

refractive index

n20/D 1.462 (lit.)

refractive index

n20/D 1.462 (lit.)

refractive index

-

bp

194-197 °C/720 mmHg (lit.)

bp

194-197 °C/720 mmHg (lit.)

bp

194-197 °C/720 mmHg (lit.)

bp

-

density

0.87 g/mL at 25 °C (lit.)

density

0.87 g/mL at 25 °C (lit.)

density

0.87 g/mL at 25 °C (lit.)

density

0.86 g/cm3 at 20 °C

Quality Level

100

Quality Level

300

Quality Level

-

Quality Level

200

Application

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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25G
Pack Size/Quantity

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705578-5MG-PW

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MMYOMAG-74K-13

1000309185

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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)
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
Shiau-Wei Chen et al.
Journal of agricultural and food chemistry, 60(32), 7824-7829 (2012-07-05)
Neuropeptide Y (NPY) is the most important appetite regulator. This study aimed to establish an in vitro NPY mRNA expression model for screening essences to determine if they are an appetite stimulator or inhibitor. We cultured the olfactory nerve cells
Bing-Ho Cheng et al.
Journal of agricultural and food chemistry, 60(31), 7623-7628 (2012-07-10)
Cinnamomum osmophloeum ct. linalool is one of the chemotypes of the indigenous cinnamon in Taiwan. In this study, hydrodistillation was used for extracting the essential oils (EOs) of C. osmophloeum ct. linalool leaves collected from various plants and seasons, and

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