carene
carene structure
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Common Name | carene | ||
|---|---|---|---|---|
| CAS Number | 13466-78-9 | Molecular Weight | 136.234 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 171.4±0.0 °C at 760 mmHg | |
| Molecular Formula | C10H16 | Melting Point | 25°C | |
| MSDS | Chinese USA | Flash Point | 46.1±0.0 °C | |
| Symbol |
GHS02, GHS07, GHS08 |
Signal Word | Danger | |
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Genotoxic, antigenotoxic and antioxidant properties of methanol extracts obtained from Peltigera horizontalis and Peltigera praetextata.
Toxicol. Ind. Health 31 , 602-13, (2015) Now-a-days, there is a big need to reduce genotoxic effects of mutagenic and carcinogenic agents in environment, which are increased by the technological development. Lichens produce a wide variety of unique metabolites due to being in various extreme areas a... |
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Emission characteristics of VOCs emitted from consumer and commercial products and their ozone formation potential.
Environ. Sci. Pollut. Res. Int. 22 , 9345-55, (2015) The characteristics of volatile organic compounds (VOCs) emitted from several consumer and commercial products (body wash, dishwashing detergent, air freshener, windshield washer fluid, lubricant, hair spray, and insecticide) were studied and compared. The sp... |
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Mechanisms for the formation of organic acids in the gas-phase ozonolysis of 3-carene.
Phys. Chem. Chem. Phys. 11(21) , 4184-97, (2009) This paper describes experimental studies aimed at elucidating mechanisms for the formation of low-volatility organic acids in the gas-phase ozonolysis of 3-carene. Experiments were carried out in a static chamber under 'OH-free' conditions. A range of multif... |
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Antioxidant and antiacetylcholinesterase activities of some commercial essential oils and their major compounds.
Molecules 16(9) , 7672-90, (2011) The commercial essential oils of Citrus aurantium L., Cupressus sempervirens L., Eucalyptus globulus Labill., Foeniculum vulgare Mill. and Thymus vulgaris L., isolated by steam distillation by a company of Morocco were evaluated in terms of in vitro antioxida... |
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Asymmetric synthesis of α-methyl-α-amino acids via diastereoselective alkylation of (1S)-(+)-3-carene derived tricyclic iminolactone.
J. Org. Chem. 76(6) , 1621-33, (2011) A novel carene-based alanine-equivalent tricyclic iminolactone 16 has been synthesized via stereoselective dihydroxylation of the double bond, IBX oxidation of the secondary alcohol, esterification of the tertiary alcohol, deprotection of the resulting ester,... |
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Sensitive monitoring of monoterpene metabolites in human urine using two-step derivatisation and positive chemical ionisation-tandem mass spectrometry.
Anal. Chim. Acta 793 , 26-36, (2013) A gas chromatographic-positive chemical ionisation-tandem mass spectrometric (GC-PCI-MS/MS) method for the simultaneous determination of 10 oxidative metabolites of the monoterpenoid hydrocarbons α-pinene, (R)-limonene, and Δ(3)-carene ((+)-3-carene) in human... |
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Low concentration of 3-carene stimulates the differentiation of mouse osteoblastic MC3T3-E1 subclone 4 cells.
Phytother Res. 22(1) , 18-22, (2008) Recently, natural products have gained more interest as alternative treatments for metabolic bone disorders and for the maintenance of bone health. In this study, the anabolic activities of 89 natural compounds were evaluated by measuring the amount of newly ... |
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Genotoxicity of citrus wastewater in prokaryotic and eukaryotic cells and efficiency of heterogeneous photocatalysis by TiO(2).
J. Photochem. Photobiol. B, Biol. 108 , 8-15, (2012) The presence of (±)α-pinene, (+)β-pinene, (+)3-carene, and R-(+)limonene terpenes in wastewater of a citrus transformation factory was detected and analyzed, in a previous study, by using Solid Phase Micro-extraction (SPME) followed by GC analyses. Purpose of... |
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A facile and efficient synthesis of 3,3-dimethyl isopropylidene proline from (+)-3-carene.
J. Org. Chem. 75(4) , 1285-8, (2010) A highly efficient and practical route to 3,4-isopropylidene proline I, starting from (+)-3-carene, was developed. The three continuous stereocenters were constructed using the inherent chirality of the starting natural product 2. The overall yield for the 12... |
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Physical and chemical responses of Sitka spruce (Picea sitchensis) clones to colonization by Heterobasidion annosum as potential markers for relative host susceptibility.
Tree Physiol. 27(12) , 1701-10, (2007) Forty-one 2-year-old clones of Picea sitchensis (Bong.) Carr. from three full-sib families (14 clones from each of two families and 13 clones from a third family) were either wounded and inoculated with an isolate of Heterobasidion annosum (Fr.) Bref. or woun... |