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51782

Supelco

Linalool

analytical standard

Synonym(e):

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

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About This Item

Lineare Formel:
(CH3)2C=CHCH2CH2C(CH3)(OH)CH=CH2
CAS-Nummer:
78-70-6
Molekulargewicht:
154.25
Beilstein:
1721488
EG-Nummer:
201-134-4
MDL-Nummer:
MFCD00008906
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329757741
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Dampfdruck

0.17 mmHg ( 25 °C)

Assay

≥99.0% (GC)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.462 (lit.)

bp

194-197 °C/720 mmHg (lit.)

Dichte

0.87 g/mL at 25 °C (lit.)

Anwendung(en)

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

Format

neat

Lagertemp.

2-8°C

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

InChIKey

CDOSHBSSFJOMGT-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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

Sonstige Hinweise

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

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

171.0 °F - Pensky-Martens closed cup

Flammpunkt (°C)

77.2 °C - Pensky-Martens closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG2546
BCCB5318
BCBV9757
BCBQ3395V
BCBN5403V

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(−)-Linalool ≥95.0% (sum of enantiomers, GC)

Sigma-Aldrich

62139

(−)-Linalool

Linalool for synthesis

Sigma-Aldrich

8.18627

Linalool

Linalool primary reference standard

00350190

Linalool

3-Octanon analytical standard

Supelco

46214

3-Octanon

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

Supelco

61706

Linalool

Myrcen analytical standard

Supelco

64643

Myrcen

(−)-Linalool analytical standard

Supelco

74856

(−)-Linalool

Linalool solution certified reference material, 2000 μg/mL in methanol, ampule of 1 mL

Supelco

CRM40437

Linalool solution

Linalool phyproof® Reference Substance

PHL80885

Linalool

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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GC Analysis of Spearmint Essential Oil on SLB®-IL59

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Protokolle

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-(+)-Limonene, purum, ≥98.0% (sum of enantiomers, GC); Geranyl tiglate; α-Terpineol, natural, ≥96%, FCC, FG; Geranyl formate; α-Pinene

Essential Oil on SLB®-5ms

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-Cymene; (−)-Menthone; α-Terpineol, natural, ≥96%, FCC, FG; Terpinolene; β-Bourbonene; 1-Octen-3-ol; β-Caryophyllene; Linalool; α-Terpinene; (−)-Menthol

GC Analysis of Peppermint Essential Oil on SLB®-IL59

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