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70049

Sigma-Aldrich

Myrcene

technical, ~90% (GC)

Synonym(s):

β-Myrcene, 7-Methyl-3-methylene-1,6-octadiene

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About This Item

Linear Formula:
H2C=CHC(=CH2)CH2CH2CH=C(CH3)2
CAS Number:
Molecular Weight:
136.23
Beilstein:
1719990
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

vapor density

4.7 (vs air)

vapor pressure

~7 mmHg ( 20 °C)

grade

technical

Assay

~90% (GC)

refractive index

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

bp

167 °C (lit.)

density

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

InChI key

UAHWPYUMFXYFJY-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

111.2 °F - closed cup

Flash Point(C)

44 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
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
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.

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