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70049

Sigma-Aldrich

Myrcen

technical, ~90% (GC)

Synonym(e):

β-Myrcen, 7-Methyl-3-methylen-1,6-octadien

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About This Item

Lineare Formel:
H2C=CHC(=CH2)CH2CH2CH=C(CH3)2
CAS-Nummer:
123-35-3
Molekulargewicht:
136.23
Beilstein:
1719990
EG-Nummer:
204-622-5
MDL-Nummer:
MFCD00008908
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24886043

Dampfdichte

4.7 (vs air)

Dampfdruck

~7 mmHg ( 20 °C)

Qualität

technical

Assay

~90% (GC)

Brechungsindex

n20/D 1.469 (lit.)
n20/D 1.469

bp

167 °C (lit.)

Dichte

0.791 g/mL at 25 °C (lit.)

SMILES String

C\C(C)=C/CCC(=C)C=C

InChI

1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3

InChIKey

UAHWPYUMFXYFJY-UHFFFAOYSA-N

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Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

M100005

Myrcen, technical grade

Signalwort

Danger

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

111.2 °F - closed cup

Flammpunkt (°C)

44 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Analysenzertifikate (COA)

Lot/Batch Number

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Osman Ciftci et al.
Toxicology and industrial health, 27(5), 447-453 (2011-01-20)
The aim of this study was to investigate the effectiveness of curcumin, β-myrcene (myrcene) and 1,8-cineole (cineole) on antioxidant defense system in rats given a persistent environmental pollutant (2,3,7,8-tetrachlorodibenzo-p-dioxin, TCDD). Rats (n = 112) were divided randomly into 8 equal
Josep-Salvador Blanch et al.
Physiologia plantarum, 131(2), 211-225 (2008-02-07)
We studied the effects of water stress, fertilization and time course on foliar volatile terpene emission rates by Quercus ilex and Pinus halepensis in a garden experiment. The terpenes mostly emitted by both species were alpha-pinene, beta-pinene, beta-myrcene and Delta(3)-carene.
Pedro M Santos et al.
Proteomics, 9(22), 5101-5111 (2009-10-03)
Beta-myrcene, a monoterpene widely used as a fragrance and flavoring additive, also possesses analgesic, anti-mutagenic, and tyrosinase inhibitory properties. In order to get insights into the molecular mechanisms underlying the ability of Pseudomonas sp. M1 to catabolize beta-myrcene, an expression
Johannes Stökl et al.
Proceedings. Biological sciences, 278(1709), 1216-1222 (2010-10-15)
Most insects are dependent on chemical communication for activities such as mate finding or host location. Several plants, and especially orchids, mimic insect semiochemicals to attract insects for unrewarded pollination. Here, we present a new case of pheromone mimicry found
Akbar Esmaeili et al.
Chemistry Central journal, 5, 26-26 (2011-05-26)
Dihydrolinalool and terpineol are sources of fragrances that provide a unique volatile terpenoid alcohol of low toxicity and thus are widely used in the perfumery industry, in folk medicine, and in aromatherapy. They are important chemical constituents of the essential
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