Myrcene

Myrcene^[1]
Names
	Preferred IUPAC name 7-Methyl-3-methylideneocta-1,6-diene
Identifiers
CAS Number	123-35-3 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:17221 ;
ChEMBL	ChEMBL455491 ;
ChemSpider	28993 ;
ECHA InfoCard	100.004.203
KEGG	C06074 ;
PubChem CID	31253;
UNII	3M39CZS25B ;
CompTox Dashboard (EPA)	DTXSID6025692 ;
	InChI InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3 Key: UAHWPYUMFXYFJY-UHFFFAOYSA-N ; InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3 Key: UAHWPYUMFXYFJY-UHFFFAOYAT;
	SMILES CC(=CCCC(=C)C=C)C;
Properties
Chemical formula	C10H16
Molar mass	136.238 g·mol−1
Density	0.794 g/cm3
Melting point	< −10 °C (14 °F; 263 K)
Boiling point	166 to 168 °C (331 to 334 °F; 439 to 441 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Myrcene, or β-myrcene, is a monoterpene. A colorless oil, it occurs widely in essential oils. It is produced mainly semi-synthetically from Myrcia, from which it gets its name. It is an intermediate in the production of several fragrances.^[3] An less-common isomeric form, having one of the three alkene units in a different position, is α-myrcene.

^ Merck Index, 11th Edition, 6243
^ Cite error: The named reference Ullmann was invoked but never defined (see the help page).
^ Behr, A.; Johnen, L. (2009). "Myrcene as a Natural Base Chemical in Sustainable Chemistry: A Critical Review". ChemSusChem. 2 (12): 1072–1095. Bibcode:2009ChSCh...2.1072B. doi:10.1002/cssc.200900186. PMID 20013989.

[1] Merck Index, 11th Edition, 6243

[Ullmann-2] Cite error: The named reference Ullmann was invoked but never defined (see the help page).

[Behr-3] Behr, A.; Johnen, L. (2009). "Myrcene as a Natural Base Chemical in Sustainable Chemistry: A Critical Review". ChemSusChem. 2 (12): 1072–1095. Bibcode:2009ChSCh...2.1072B. doi:10.1002/cssc.200900186. PMID 20013989.

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