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Details

Stereochemistry ACHIRAL
Molecular Formula C10H16
Molecular Weight 136.2344
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRCENE

SMILES

C=CC(=C)CCC=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 136.2344
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Defensive chemistry of an aposematic bug, Pachycoris stallii Uhler and volatile compounds of its host plant Croton californicus Muell.-Arg.
2001 Feb
Antifungal activity of the components of Melaleuca alternifolia (tea tree) oil.
2003
A novel sex-specific and inducible monoterpene synthase activity associated with a pine bark beetle, the pine engraver, Ips pini.
2003 Apr
Character impact odorants of Citrus Hallabong [(C. unshiu Marcov x C. sinensis Osbeck) x C. reticulata Blanco] cold-pressed peel oil.
2003 Apr 23
Differences in the fragrances of pollen, leaves, and floral parts of garland (Chrysanthemum coronarium) and composition of the essential oils from flowerheads and leaves.
2003 Apr 9
Bacterial susceptibility to and chemical composition of essential oils from Thymus kotschyanus and Thymus persicus.
2003 Apr 9
Composition and antibacterial activity of the essential oils from Zanthoxylum rhoifolium.
2003 Aug
Evaluation of anti-inflammatory activity of essential oils from two Asteraceae species.
2003 Aug
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
Antispasmodic effect of the essential oil of Plectranthus barbatus and some major constituents on the guinea-pig ileum.
2003 Dec
Monoterpenes produced by Cupressus lusitanica cultured cells including a novel monoterpene (1R, 2S, 6S)-(+)-1,6-epoxy-4(8)-p-menthen-2-ol [corrected].
2003 Dec
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
Composition and antimicrobial activity of Achillea clavennae L. essential oil.
2003 Nov
Analysis of essential oil of Coridothymus capitatus (L.) and its antibacterial and antifungal activity.
2003 Sep-Oct
Content and composition of the essential oil of Thymus serpyllum L. growing wild in Estonia.
2004
[The crop-producing power and chemical composition of the essential oil of the cones of hop cultivars].
2004
Behavioral response of Lygus hesperus to conspecifics and headspace volatiles of alfalfa in a Y-tube olfactometer.
2004 Aug
Analysis of volatiles in porcine liver pâtés with added sage and rosemary essential oils by using SPME-GC-MS.
2004 Aug 11
cDNA isolation and functional expression of myrcene synthase from Perilla frutescens.
2004 Dec
Analysis of volatile secondary metabolites from Colombian Xylopia aromatica (Lamarck) by different extraction and headspace methods and gas chromatography.
2004 Jan 30
Essential oils of the leaves of the Raukaua genus (Araliaceae).
2004 Jan-Feb
Mono and diterpene production in Escherichia coli.
2004 Jul 20
Novel diterpenes from the heartwood of Chamaecyparis obtusa var. formosana.
2004 Jun
Comparative analysis of the oil and supercritical CO2 extract of Elettaria cardamomum (L.) Maton.
2004 Oct 6
Comparison of terpene composition in Engelmann spruce (Picea engelmannii) using hydrodistillation, SPME and PLE.
2004 Sep-Oct
Chemical composition and anticancer activity of leaf essential oil of Myrica gale L.
2005 Apr
Volatile organic compounds produced during the aerobic biological processing of municipal solid waste in a pilot plant.
2005 Apr
Application of artificial neural network on mono- and sesquiterpenes compounds determined by headspace solid-phase microextraction-gas chromatography-mass spectrometry for the Piedmont ricotta cheese traceability.
2005 Apr 15
Changes in anatomy and terpene chemistry in roots of Douglas-fir seedlings following treatment with methyl jasmonate.
2005 Aug
Evolution of aroma compounds from orange juice stored in polyethylene terephthalate (PET).
2005 Feb
Intensity and the ratios of compounds in the scent of snapdragon flowers affect scent discrimination by honeybees (Apis mellifera).
2005 Feb
Biosynthesis of mono- and sesquiterpenes in carrot roots and leaves (Daucus carota L.): metabolic cross talk of cytosolic mevalonate and plastidial methylerythritol phosphate pathways.
2005 Feb
Evaluation of beta-myrcene, alpha-terpinene and (+)- and (-)-alpha-pinene in the Salmonella/microsome assay.
2005 Feb
Screening for key odorants in Moroccan green olives by gas chromatography-olfactometry/aroma extract dilution analysis.
2005 Feb 23
In vivo antimalarial activity of essential oils from Cymbopogon citratus and Ocimum gratissimum on mice infected with Plasmodium berghei.
2005 Jan
Mastrus ridibundus parasitoids eavesdrop on cocoon-spinning codling moth, Cydia pomonella, larvae.
2005 Jan
The effect of terpenoid extracts from 15 pine species on the feeding behavioural sequence of the late instars of the pine processionary caterpillar Thaumetopoea pityocampa.
2005 Jun 30
Characteristic odor components of kumquat (Fortunella japonica Swingle) peel oil.
2005 Mar 9
The essential oils from Zanthoxylum schinifolium pericarp induce apoptosis of HepG2 human hepatoma cells through increased production of reactive oxygen species.
2005 May
Stability and sensory shelf life of orange juice pasteurized by continuous ohmic heating.
2005 May 18
Bioactive compounds of grapefruit (Citrus paradisi Cv. Rio Red) respond differently to postharvest irradiation, storage, and freeze drying.
2005 May 18
Systemic induction of volatile release in cotton: how specific is the signal to herbivory?
2005 Oct
Patents
Substance Class Chemical
Created
by admin
on Sat Jun 26 02:42:16 UTC 2021
Edited
by admin
on Sat Jun 26 02:42:16 UTC 2021
Record UNII
3M39CZS25B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MYRCENE
FCC   FHFI   HSDB  
Common 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
MYRCENE [INCI]
Common Name English
.BETA.-MYRCENE
MI  
Systematic 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 Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
CFR 21 CFR 172.515
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
DSLD 4190 (Number of products:2)
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
JECFA EVALUATION MYRCENE
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
Code System Code Type Description
HSDB
1258
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
FDA UNII
3M39CZS25B
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
RXCUI
2166047
Created by admin on Sat Jun 26 02:42:17 UTC 2021 , Edited by admin on Sat Jun 26 02:42:17 UTC 2021
PRIMARY
CAS
123-35-3
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
WIKIPEDIA
MYRCENE
Created by admin on Sat Jun 26 02:42:17 UTC 2021 , Edited by admin on Sat Jun 26 02:42:17 UTC 2021
PRIMARY
MESH
C509595
Created by admin on Sat Jun 26 02:42:17 UTC 2021 , Edited by admin on Sat Jun 26 02:42:17 UTC 2021
PRIMARY
PUBCHEM
31253
Created by admin on Sat Jun 26 02:42:17 UTC 2021 , Edited by admin on Sat Jun 26 02:42:17 UTC 2021
PRIMARY
EPA CompTox
123-35-3
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
EVMPD
SUB62723
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
ECHA (EC/EINECS)
204-622-5
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY
MERCK INDEX
M7686
Created by admin on Sat Jun 26 02:42:16 UTC 2021 , Edited by admin on Sat Jun 26 02:42:16 UTC 2021
PRIMARY Merck Index
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