2-carene
3,7,7-trimethylbicyclo[4.1.0]hept-2-ene
Identification
| Name | 2-carene |
| IUPAC | 4,7,7-trimethylbicyclo[4.1.0]hept-4-ene |
| CAS Number | 554-61-0 |
| FDA UNII | F03R774450 |
| Molecular Formula | C10 H16 |
| Molecular Weight | 136.23752000 |
| Nikkaji Number | J109.974D |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 167.00 to 168.00 °C. @ 760.00 mm Hg |
| Vapor Pressure | 3.720000 mmHg (est) |
| Flash Point | 101.00 °F. TCC ( 38.30 °C. ) (est) |
| logP (o/w) | 4.440 |
| Soluble in | alcohol |
| Insoluble in | water |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 2-carene usage levels up to | not for fragrance use. |
| Recommendation for 2-carene flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
bicyclo(4.1.0)hept-2-ene, 3,7,7-trimethyl-
bicyclo[4.1.0]hept-2-ene, 3,7,7-trimethyl-
car-2-ene
(±)-
car-2-ene
(±)-2-
carene
alpha-
carene
3,7,7-
trimethyl bicyclo(4.1.0)hept-2-ene
3,7,7-
trimethylbicyclo[4.1.0]hept-2-en
3,7,7-
trimethylbicyclo[4.1.0]hept-2-ene
4,7,7-
trimethylbicyclo[4.1.0]hept-4-ene
PubMed:
Comparison of chemical compositions and antimicrobial activities of essential oils from three conifer trees; Pinus densiflora, Cryptomeria japonica, and Chamaecyparis obtusa.
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Analysis of the essential oil from the roots of Eupatorium cannabinum subsp. corsicum (L.) by GC, GC-MS and 13C-NMR.
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Chemical composition, cytotoxicity and in vitro antitrypanosomal and antiplasmodial activity of the essential oils of four Cymbopogon species from Benin.
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Cryotrap/SPME/GC/MS method for profiling of monoterpenes in cheese and their clustering according to geographic origin.
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Chemical composition and antioxidant properties of Laurus nobilis L. and Myrtus communis L. essential oils from Morocco and evaluation of their antimicrobial activity acting alone or in combined processes for food preservation.
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A tale of two carenes: intrinsic optical activity and large-amplitude nuclear displacement.
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Biotransformation of (1S)-2-carene and (1S)-3-carene by Picea abies suspension culture.
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Analysis of roasted and unroasted Pistacia terebinthus volatiles using direct thermal desorption-GCxGC-TOF/MS.
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Attraction and oviposition of Tuta absoluta females in response to tomato leaf volatiles.
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Monoterpene-based chiral β-amino acid derivatives prepared from natural sources: syntheses and applications.
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Composition of essential oil of Chinese Chenopodium ambrosioides and insecticidal activity against maize weevil, Sitophilus zeamais.
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Lippia javanica (Burm F) Spreng: its general constituents and bioactivity on mosquitoes.
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Comparison of chemical compositions and antimicrobial activities of essential oils from three conifer trees; Pinus densiflora, Cryptomeria japonica, and Chamaecyparis obtusa.
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Formation and stability of secondary ozonides from monoterpenes studied by mass spectrometry.
PubMed:
Analysis of the essential oil from the roots of Eupatorium cannabinum subsp. corsicum (L.) by GC, GC-MS and 13C-NMR.
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Enantiospecific syntheses of C(5)-functionalized precursors of artemisinin derivatives.
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Platinum- and gold-catalyzed rearrangement reactions of propargyl acetates: total syntheses of (-)-alpha-cubebene, (-)-cubebol, sesquicarene and related terpenes.
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Response factor considerations for the quantitative analysis of western redcedar (Thuja plicata) foliar monoterpenes.
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Thiol-catalysed radical-chain redox rearrangement reactions of benzylidene acetals derived from terpenoid diols.
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Synthesis of new chiral 2,2'-bipyridine ligands and their application in copper-catalyzed asymmetric allylic oxidation and cyclopropanation.
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Production of beta-thujaplicin in Cupressus lusitanica suspension cultures fed with organic acids and monoterpenes.
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Alcaligenes defragrans sp. nov., description of four strains isolated on alkenoic monoterpenes ((+)-menthene, alpha-pinene, 2-carene, and alpha-phellandrene) and nitrate.
PubMed:
Microbial degradation of monoterpenes in the absence of molecular oxygen.