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51782

Supelco

Linalool

analytical standard

Sinônimo(s):

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

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About This Item

Fórmula linear:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
Número CAS:
78-70-6
Peso molecular:
154.25
Beilstein:
1721488
Número CE:
201-134-4
Número MDL:
MFCD00008906
Código UNSPSC:
85151701
ID de substância PubChem:
329757741
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

pressão de vapor

0.17 mmHg ( 25 °C)

Ensaio

≥99.0% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.462 (lit.)

pb

194-197 °C/720 mmHg (lit.)

densidade

0.87 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

CDOSHBSSFJOMGT-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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

Outras notas

This compound is commonly found in plants of the genus: cinnamomum salvia thymus

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H317,H319

Classificações de perigo

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

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

171.0 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

77.2 °C - Pensky-Martens closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCG2546
BCCB5318
BCBV9757
BCBQ3395V
BCBN5403V

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L-Linalool natural, ≥95%, FG

Sigma-Aldrich

W263516

L-Linalool

Mirceno analytical standard

Supelco

64643

Mirceno

Geraniol analytical standard

Supelco

48798

Geraniol

Linalyl acetate ≥97%, FCC, FG

Sigma-Aldrich

W263605

Linalyl acetate

3-Octanone analytical standard

Supelco

46214

3-Octanone

(R)-(+)-Limonene analytical standard

Supelco

62118

(R)-(+)-Limonene

Methyl eugenol analytical standard

Supelco

04607

Methyl eugenol

α-Terpineol analytical standard

Supelco

04899

α-Terpineol

Estragole analytical standard

Supelco

34098

Estragole

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
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