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Details

Stereochemistry ACHIRAL
Molecular Formula C10H16
Molecular Weight 136.234
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRCENE

SMILES

CC(C)=CCCC(=C)C=C

InChI

InChIKey=UAHWPYUMFXYFJY-UHFFFAOYSA-N
InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3

HIDE SMILES / InChI

Molecular Formula C10H16
Molecular Weight 136.234
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanism of monoterpene cyclization: stereochemical aspects of the transformation of noncyclizable substrate analogs by recombinant (-)-limonene synthase, (+)-bornyl diphosphate synthase, and (-)-pinene synthase.
2001 Aug 1
Correspondence of soldier defense secretion mixtures with cuticular hydrocarbon phenotypes for chemotaxonomy of the termite genus Reticulitermes in North America.
2001 Jul
Fungitoxic activity of 12 essential oils against four postharvest citrus pathogens: chemical analysis of thymus capitatus oil and its effect in subatmospheric pressure conditions.
2001 Jul
Effects of four mono- and sesquiterpenes on the consumption of alfalfa pellets by sheep.
2002 Dec
Composition and seasonal variation of the essential oil from leaves and peel of a Cretan lemon variety.
2002 Jan 2
Volatile chemicals identified in extracts from newly hybrid citrus, dekopon (Shiranuhi mandarin Suppl. J.).
2002 Sep 11
Antifungal activity of the components of Melaleuca alternifolia (tea tree) oil.
2003
Analysis of some Italian lemon liquors (limoncello).
2003 Aug 13
Changes in volatile compounds of carrots (Daucus carota L.) during refrigerated and frozen storage.
2003 Aug 27
Influence of flavour absorption by food-packaging materials (low-density polyethylene, polycarbonate and polyethylene terephthalate) on taste perception of a model solution and orange juice.
2003 Jan
Microcapsules from starch granules.
2003 Jan-Feb
Metabolic flux analysis of halogenated monoterpene biosynthesis in microplantlets of the macrophytic red alga Ochtodes secundiramea.
2003 Jul
Composition and antimicrobial properties of Sardinian Juniperus essential oils against foodborne pathogens and spoilage microorganisms.
2003 Jul
Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage.
2003 Jul 2
Isolation of halogenated monoterpenes from bioreactor-cultured microplantlets of the macrophytic red algae Ochtodes secundiramea and Portieria hornemannii.
2003 Jun
Characterization of volatiles in bullock's heart (Annona reticulata L.) fruit cultivars from Cuba.
2003 Jun 18
(E)-beta-ocimene and myrcene synthase genes of floral scent biosynthesis in snapdragon: function and expression of three terpene synthase genes of a new terpene synthase subfamily.
2003 May
Identification of aroma active compounds in orange essence oil using gas chromatography-olfactometry and gas chromatography-mass spectrometry.
2003 May 23
Chemical composition of the essential oils of Juniperus from ripe and unripe berries and leaves and their antimicrobial activity.
2003 May 7
Content and composition of the essential oil of Thymus serpyllum L. growing wild in Estonia.
2004
Behavioral response of Lygus hesperus to conspecifics and headspace volatiles of alfalfa in a Y-tube olfactometer.
2004 Aug
cDNA isolation and functional expression of myrcene synthase from Perilla frutescens.
2004 Dec
The effect of selected monoterpenoids on the cellular slime mold, Dictyostelium discoideum NC4.
2004 Jun
Comparative analysis of the oil and supercritical CO2 extract of Elettaria cardamomum (L.) Maton.
2004 Oct 6
Chemical composition and anticancer activity of leaf essential oil of Myrica gale L.
2005 Apr
Changes in anatomy and terpene chemistry in roots of Douglas-fir seedlings following treatment with methyl jasmonate.
2005 Aug
Associative learning of plant odorants activating the same or different receptor neurones in the moth Heliothis virescens.
2005 Feb
Screening for key odorants in Moroccan green olives by gas chromatography-olfactometry/aroma extract dilution analysis.
2005 Feb 23
Chemical composition, antibacterial and antifungal activities of the essential oil of Haplophyllum tuberculatum from Oman.
2005 Jan 4
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:09:32 GMT 2025
Edited
by admin
on Mon Mar 31 20:09:32 GMT 2025
Record UNII
3M39CZS25B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MYRCENE
FCC   FHFI   HSDB  
INCI  
Official Name English
.BETA.-MYRCENE
MI  
Preferred Name English
.BETA.-MYRCENE [IARC]
Common Name English
NSC-406264
Code English
1,6-OCTADIENE, 7-METHYL-3-METHYLENE-
Systematic Name English
.BETA.-GERANIOLENE
Common Name English
7-METHYL-3-METHYLENE-1,6-OCTADIENE
Systematic Name English
MYRCENE [FCC]
Common Name English
DECATRIENE
Systematic Name English
MYRCENE [FHFI]
Common Name English
FEMA NO. 2762
Code English
MYRCENE [HSDB]
Common Name English
.BETA.-MYRCENE [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 125901
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
DSLD 4190 (Number of products:2)
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
JECFA EVALUATION MYRCENE
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
Code System Code Type Description
NSC
406264
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
HSDB
1258
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
DAILYMED
3M39CZS25B
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
FDA UNII
3M39CZS25B
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
RXCUI
2166047
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
CAS
123-35-3
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
WIKIPEDIA
MYRCENE
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
MESH
C509595
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
PUBCHEM
31253
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
JECFA MONOGRAPH
1326
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID6025692
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
CHEBI
17221
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
EVMPD
SUB62723
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
SMS_ID
100000134489
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-622-5
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY
MERCK INDEX
m7686
Created by admin on Mon Mar 31 20:09:32 GMT 2025 , Edited by admin on Mon Mar 31 20:09:32 GMT 2025
PRIMARY Merck Index
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