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51782

Supelco

Linalool

analytical standard

Sinónimos:

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

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About This Item

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

grado

analytical standard

Nivel de calidad

100

presión de vapor

0.17 mmHg ( 25 °C)

Ensayo

≥99.0% (GC)

caducidad

limited shelf life, expiry date on the label

técnicas

HPLC: suitable
gas chromatography (GC): suitable

índice de refracción

n20/D 1.462 (lit.)

bp

194-197 °C/720 mmHg (lit.)

densidad

0.87 g/mL at 25 °C (lit.)

aplicaciones

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

Formato

neat

temp. de almacenamiento

2-8°C

cadena 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

Clave InChI

CDOSHBSSFJOMGT-UHFFFAOYSA-N

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Descripción general

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.

Aplicación

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

Otras notas

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

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H315,H317,H319

Clasificaciones de peligro

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

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

171.0 °F - Pensky-Martens closed cup

Punto de inflamabilidad (°C)

77.2 °C - Pensky-Martens closed cup

Equipo de protección personal

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
BCCL6154
BCCG2546
BCCB5318
BCBV9757
BCBQ3395V

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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
A T Peana et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 9(8), 721-726 (2003-02-18)
Linalool and linalyl acetate are the principal components of many essential oils known to possess several biological activities, attributable to these monoterpene compounds. In this work, we evaluated individually the anti-inflammatory properties of (-) linalool, that is, the natural occurring
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