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Details

Stereochemistry RACEMIC
Molecular Formula C10H16
Molecular Weight 136.234
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-CARENE

SMILES

CC1=CC[C@H]2[C@@H](C1)C2(C)C

InChI

InChIKey=BQOFWKZOCNGFEC-DTWKUNHWSA-N
InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H16
Molecular Weight 136.234
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparing the variation of needle and wood terpenoids in Scots pine provenances.
2002 Jan
Exposure assessment to alpha- and beta-pinene, delta(3)-carene and wood dust in industrial production of wood pellets.
2003 Apr
A cDNA clone for 3-carene synthase from Salvia stenophylla.
2003 Apr
Antioxidative properties of the essential oil from Pinus mugo.
2003 Dec 17
Traumatic resin defense in Norway spruce (Picea abies): methyl jasmonate-induced terpene synthase gene expression, and cDNA cloning and functional characterization of (+)-3-carene synthase.
2003 Jan
Respiratory symptoms and occupational exposures in New Zealand plywood mill workers.
2003 Jun
Identification of plant odours activating receptor neurones in the weevil Pissodes notatus F. (Coleoptera, Curculionidae).
2003 Mar
Effects of monoterpenoids, acting alone or in pairs, on seed germination and subsequent seedling growth.
2003 Oct
An experimental comparison of a kinetic model for the reaction of alpha-pinene and Delta(3)-carene with ozone and nitrogen oxides.
2004
Butyryl- and acetyl-cholinesterase inhibitory activities in essential oils of Salvia species and their constituents.
2004 Apr
Mono and diterpene production in Escherichia coli.
2004 Jul 20
Study of the carbonyl products of terpene/OH radical reactions: detection of the 2,4-DNPH derivatives by HPLC-MS.
2004 Jun
Full-scale chamber investigation and simulation of air freshener emissions in the presence of ozone.
2004 May 15
Identification of the larval aggregation pheromone of codling moth, Cydia pomonella.
2005 Apr
Olfactory receptor neurons in two Heliothine moth species responding selectively to aliphatic green leaf volatiles, aromatic compounds, monoterpenes and sesquiterpenes of plant origin.
2005 Jun
Inhibition of acetylcholinesterase activity by bicyclic monoterpenoids.
2005 Mar 9
Atmospheric fate of OH initiated oxidation of terpenes. Reaction mechanism of alpha-pinene degradation and secondary organic aerosol formation.
2005 May
Continuous real-time analysis of products from the reaction of some monoterpenes with ozone using atmospheric sampling glow discharge ionization coupled to a quadrupole ion trap mass spectrometer.
2005 May 15
Host selection in Tomicus piniperda L.: composition of monoterpene hydrocarbons in relation to attack frequency in the shoot feeding phase.
2006 May-Jun
Response to host volatiles by native and introduced populations of Dendroctonus valens (Coleoptera: Curculionidae, Scolytinae) in North America and China.
2007 Jan
The role of genetic and chemical variation of Pinus sylvestris seedlings in influencing slug herbivory.
2007 May
Synergistic blends of monoterpenes for aggregation pheromones of the mountain pine beetle (Coleoptera: Curculionidae).
2008 Aug
Influence of OH scavenger on the water effect on secondary organic aerosol formation from ozonolysis of limonene, Delta3-carene, and alpha-pinene.
2008 Aug 15
Content, composition, and bioactivity of the essential oils of three basil genotypes as a function of harvesting.
2008 Jan 23
Chemical composition and antimicrobial activity of essential oil from cones of Pinus koraiensis.
2008 Mar
Digital, Three-dimensional Average Shaped Atlas of the Heliothis Virescens Brain with Integrated Gustatory and Olfactory Neurons.
2009
Evaluation of monoterpenes for the control of Tribolium castaneum (Herbst) and Sitophilus zeamaise Motschulsky.
2009
Lippia javanica (Burm F) Spreng: its general constituents and bioactivity on mosquitoes.
2009 Apr
Formation and stability of secondary ozonides from monoterpenes studied by mass spectrometry.
2009 Jul
Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene.
2009 Jun 7
Radical Scavenging Activity of the Essential Oil of Silver Fir (Abies alba).
2009 May
Formaldehyde in the indoor environment.
2010 Apr 14
The influence of Ceratocystis polonica inoculation and methyl jasmonate application on terpene chemistry of Norway spruce, Picea abies.
2010 Aug
Complex interactions among host pines and fungi vectored by an invasive bark beetle.
2010 Aug
Characterization of delta-guaiene synthases from cultured cells of Aquilaria, responsible for the formation of the sesquiterpenes in agarwood.
2010 Dec
Comparison of FTIR and particle mass spectrometry for the measurement of particulate organic nitrates.
2010 Feb 1
Pyrazole derived from (+)-3-carene; a novel potent, selective scaffold for sphingosine-1-phosphate (S1P(1)) receptor agonists.
2010 Jan 1
Cytotoxicity and genotoxicity in human lung epithelial A549 cells caused by airborne volatile organic compounds emitted from pine wood and oriented strand boards.
2010 Jun 16
Regio- and stereoselective oxidation of (+)-Delta(3)-carene by the larvae of common cutworm (Spodoptera litura).
2010 Mar 24
Evolution of the volatile compounds of ripened sausages as a function of both storage time and composition of packaging atmosphere.
2010 Nov
Genetics, phosphorus availability, and herbivore-derived induction as sources of phenotypic variation of leaf volatile terpenes in a pine species.
2010 Oct
Development and validation by accuracy profile of a method for the analysis of monoterpenes in indoor air by active sampling and thermal desorption-gas chromatography-mass spectrometry.
2010 Sep 15
Substance Class Chemical
Created
by admin
on Fri Dec 15 22:08:25 GMT 2023
Edited
by admin
on Fri Dec 15 22:08:25 GMT 2023
Record UNII
H2M15SNR6N
Record Status Validated (UNII)
Record Version
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Name Type Language
3-CARENE
FHFI   MI  
Systematic Name English
.DELTA.3-CARENE
Common Name English
3-KAREN
Common Name English
BICYCLO(4.1.0)HEPT-3-ENE, 3,7,7-TRIMETHYL-
Systematic Name English
3-CARENE [MI]
Common Name English
3-CARENE [FHFI]
Common Name English
(±)-.DELTA.3-CARENE
Common Name English
3-NORCARENE, 3,7,7-TRIMETHYL-
Systematic Name English
3,7,7-TRIMETHYLBICYCLO(4.1.0)HEPT-3-ENE
Systematic Name English
S-3-CARENE
Common Name English
FEMA NO. 3821
Code English
(±)-3-CARENE
Systematic Name English
Code System Code Type Description
DAILYMED
H2M15SNR6N
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
RXCUI
2395760
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
CHEBI
35661
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
MERCK INDEX
m3105
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
3-Carene
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
FDA UNII
H2M15SNR6N
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
CAS
13466-78-9
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
MESH
C030218
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
PUBCHEM
442461
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
JECFA MONOGRAPH
1341
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID4047462
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
ECHA (EC/EINECS)
236-719-3
Created by admin on Fri Dec 15 22:08:25 GMT 2023 , Edited by admin on Fri Dec 15 22:08:25 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
Cannabis essential oil terpenoid.