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W263516

Sigma-Aldrich

L-Linalool

greener alternative

natural, ≥95%, FG

Synonym(s):

(−)-Linalool, (R)-(−)-3,7-Dimethyl-1,6-octadien-3-ol

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About This Item

Linear Formula:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS Number:
126-91-0
Molecular Weight:
154.25
FEMA Number:
2635
Beilstein/REAXYS Number:
1721487
EC Number:
204-811-2
Council of Europe no.:
61
MDL number:
MFCD00135469
UNSPSC Code:
12164502
PubChem Substance ID:
24901213
Flavis number:
2.013
NACRES:
NA.21

grade

FG
Fragrance grade
Halal
Kosher
natural

Quality Level

400

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

assay

≥95%

optical activity

[α]20/D −19.8°, neat

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

refractive index

n20/D 1.4615 (lit.)

bp

198 °C (lit.)

density

0.862 g/mL at 20 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

linalool

greener alternative category

Aligned

organoleptic

woody; floral

SMILES string

C\C(C)=C\CC[C@@](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/t10-/m0/s1

InChI key

CDOSHBSSFJOMGT-JTQLQIEISA-N

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Related Categories

General description

L-Linalool is the key volatile compound of jasmine tea, spruce essential oil and young leaves of Litchi chinensis Sonn.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

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Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

166.3 °F - closed cup

flash_point_c

74.6 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Maged E Mohamed et al.
Biomolecules, 10(11) (2020-11-01)
The monoterpene linalool is a well-known essential oil component produced by several aromatic plants. Cisplatin is a widely used anticancer drug that produces many side effects, particularly nephrotoxicity. Here, we aimed to inspect linalool's protective activity against cisplatin-induced nephrotoxicity and
Sedative effects of the jasmine tea odor and (R)-(?)-linalool, one of its major odor components, on autonomic nerve activity and mood states
Kuroda K, et al.
European Journal of Applied Physiology, 95(2-3), 107-114 (2005)
Volatile components of Litchi chinensis Sonn. leaf oil extracts obtained by simultaneous distillation extraction.
Wang YJ, et al.
Journal of Essential Oil-Bearing Plants, 16(2), 161-165 (2013)
Yasushi Hoshino et al.
Journal of biotechnology, 324, 21-27 (2020-09-28)
Linalool is a monoterpene alcohol, which imparts floral scents to a variety of plants and is extensively used in various kinds of products, such as processed foods and beverages for fragrances and flavors. However, linalool from natural resources is racemate
Behavioral and electrophysiological responses of Tetropium fuscum (Coleoptera: Cerambycidae) to pheromone and spruce volatiles.
Silk PJ, et al.
Environmental Entomology, 39(6), 1997-2005 (2010)
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