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W263508

Sigma-Aldrich

Linalool

≥97%, FCC, FG

Sinonimo/i:

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

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About This Item

Formula condensata:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
Numero CAS:
78-70-6
Peso molecolare:
154.25
Numero FEMA:
2635
Beilstein:
1721488
Numero CE:
201-134-4
N° CoE:
61
Numero MDL:
MFCD00008906
Codice UNSPSC:
12164502
ID PubChem:
24901212
Numero Flavis:
2.013
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

400

Grado

FG
Fragrance grade
Halal
Kosher

agenzia

follows IFRA guidelines
meets purity specifications of JECFA

Conformità normativa

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 182.60

Tensione di vapore

0.17 mmHg ( 25 °C)

Saggio

≥97%

Composizione

contains EU 1223/2009 restricted linalool

Indice di rifrazione

n20/D 1.462 (lit.)

P. ebollizione

194-197 °C/720 mmHg (lit.)

Solubilità

ethanol: soluble 1ml/4ml, clear, colorless (60% ethanol)

Densità

0.87 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

linalool

Organolettico

lemon; orange; floral; sweet

Stringa SMILE

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
CDOSHBSSFJOMGT-UHFFFAOYSA-N

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Descrizione generale

Linalool is a monoterepene compound. It is the major component of many essential oils. Anti-inflammatory properties of (−) linalool, a naturally occurring enantiomer, has been studied. It is also the major constituent of the basil and thyme essential oil. Linalool is reported to have a lemon like odor.
Linalool or ((±)-3,7-Dimethyl-1,6-octadien-3-ol is a reported fragrance ingredient.

Applicazioni

Linalool has been used to study the blends of various flower aroma compounds as a floral attractant for the migratory moth velvetbean caterpillar (Anticarsia gemmatalis Hübner).

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H317,H319

Classi di pericolo

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

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

171.0 °F - Pensky-Martens closed cup

Punto d’infiammabilità (°C)

77.2 °C - Pensky-Martens closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
SHBP0723
SHBN4536
STBK1931
STBK1763
STBJ8488

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Supelco

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Linalool solution

Binary floral lure attractive to velvetbean caterpillar adults (Lepidoptera: Noctuidae).
Meagher RL and Landolt PJ.
Florida entomologist, 93(1), 73-79 (2010)
H M Schellinck et al.
Chemical senses, 26(6), 663-672 (2001-07-28)
The present paper describes a quick and efficient method for assessing olfactory discrimination learning in mice. In training mice received trials in which one odor (CS+) was paired with sugar and another odor (CS-) was paired with no sugar. When
Inhibitory effect of thyme and basil essential oils, carvacrol, thymol, estragol, linalool and p-cymene towards Shigella sonnei and S. flexneri.
Bagamboula CF, et al.
Food Microbiology, 21(1), 33-42 (2004)
Transformations of monoterpenoids in aqueous acids: The reactions of linalool. geraniol, nerol and their acetates in aqueous citric acid.
Baxter RL ,et al.
Tetrahedron, 34(14), 2195-2199 (1978)
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
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