Search results for "monoterpene"

showing 10 items of 145 documents

The influence of the temperature on the liquid–liquid equlibria of the mixture limonene + ethanol + H2O

2004

Abstract In this work, experimental liquid–liquid equilibria (LLE) of the limonene + ethanol + water system are presented. The LLE of this system has been measured at 293.15, 303.15, 313.15 and 323.15 K. The equilibrium data presented are correlated using NRTL and UNIQUAC equations. Finally, the reliability of these models is tested by comparison with experimental results.

Work (thermodynamics)LimoneneEthanolUNIQUACGeneral Chemical EngineeringMonoterpeneGeneral Physics and AstronomyThermodynamicsThermodynamic modelchemistry.chemical_compoundchemistryNon-random two-liquid modelLiquid liquidPhysical and Theoretical ChemistryFluid Phase Equilibria
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Liquid–liquid equlibria of the mixture linalool+ethanol+water at different temperatures

2005

Abstract In this work, experimental liquid–liquid equilibria (LLE) data of the linalool + ethanol + water system are presented. The LLE of this system has been measured at 293.15, 303.15, 313.15 and 323.15 K. The equilibrium data presented are correlated using NRTL and UNIQUAC equations. Finally, the reliability of these models is tested by comparison with experimental results.

Work (thermodynamics)UNIQUACEthanolTernary numeral systemGeneral Chemical EngineeringMonoterpeneGeneral Physics and AstronomyThermodynamicsAlcoholchemistry.chemical_compoundLinaloolchemistryNon-random two-liquid modelPhysical and Theoretical ChemistryFluid Phase Equilibria
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Composition and antimicrobial activity of the essential oil of Achillea falcata L. (Asteraceae).

2005

The composition of the essential oil from aerial parts of Achillea falcata L. (Asteraceae) growing wild in Lebanon was analysed by GC and GC–MS; 58 compounds, representing 94.4% of the oil, were identified. Isomers of the cyclobutane ethanol, 1-methyl-2-(1-methylethenyl), grandisol (21.4%) and fragranol (16.8%) were the main components of the oil. Also abundant were artemisia ketone (5.2%), terpinen-4-ol (4.5%) and 1,8-cineole (4.0%). The essential oil shows inhibitory activity mainly against Gram-positive bacteria.

antimicrobial activityGrandisolbiologyAchilleaMonoterpeneAchillea falcataGeneral ChemistrySettore CHIM/06 - Chimica OrganicaAsteraceaeAsteraceaebiology.organism_classificationSesquiterpenegrandisolTerpenoidessential oillaw.inventionfragranolchemistry.chemical_compoundchemistrylawBotanyEssential oilFood ScienceAntibacterial agent
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Chemical composition, antioxidant and anticholinesterase activity of the essential oil of algerian cachrys sicula L

2021

In this work, in order to explore a new Algerian medicinal plant used in traditional medicine, the essential oil of the leaves of Cachrys sicula L. (Apiaceae) collected from Algeria, obtained by hydrodistillation, was analyzed by GC/MS. Thirty-two compounds were identified accounting for 98.6% of the total oil, which is characterized by a high content of monoterpene hydrocarbons (74.8%). The main constituents of the essential oil were β-pinene (17.9%), sabinene (17.8%), myrcene (12%), and α-pinene (11.4%). In vitro antioxidant activity of the essential oil was assayed by three methods, namely ABTS•+, metal chelating, and DPPH• assays. The antioxidant activity of the oil was higher in the AB…

antioxidantAntioxidantDPPHMonoterpenemedicine.medical_treatmentSabinenePlant ScienceBiochemistryessential oilAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawmedicineButyrylcholinesteraseEssential oilApiaceaeTraditional medicinebiologyOrganic ChemistryCachrys sicula Lanticholinesterasebiology.organism_classificationchemistryMyrceneGC-MSNatural Product Research
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New oxygenated eudesmanolides from artemisia herba-alba

1990

Abstract The aerial parts of Artemisia herba-alba Asso subsp.valentina Lam. (Asteraceae) yielded the new eudesmanolides 1-11 and the new sesquiterpene-monoterpene adducts 12-13. The absolute configuration of compound 6 was confirmed with the aid of X-ray diffraction analysis. Some aspects of the thermal and photochemical reactivity of 2,4-cyclohexadienones are discussed.

biologyArtemisia herba-albaStereochemistryChemistryMonoterpeneOrganic ChemistryAbsolute configurationAsteraceaebiology.organism_classificationSesquiterpeneBiochemistrychemistry.chemical_compoundDrug DiscoveryArtemisiaOrganic chemistryPhotochemical reactivityThermal reactionTetrahedron
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Composition of the essential oil ofPallenis spinosa (L.) Cass. (Asteraceae)

2003

The essential oil of Pallenis spinosa (L.) Cass. was obtained by hydrodistillation. In total 38 components were identified by GC and GC–MS. Oxygenated sesquiterpenoids amounted to 60.2% of the oil. The main components were germacra-1(10),5-dien-3,4-diol (18.4%), α-cadinol (14.1%), 3-acetoxygermacra-1(10),5-dien-4-ol (13.0%), T-cadinol (8.2%) and δ-cadinene (5.8%). The oil does not show antimicrobial activity. Copyright © 2003 John Wiley & Sons, Ltd.

biologyTraditional medicineChemistryMonoterpenePallenis spinosaGeneral ChemistryAsteraceaebiology.organism_classificationSesquiterpeneTerpenoidlaw.inventionSteam distillationchemistry.chemical_compoundCadinollawBotanyEssential oilFood ScienceFlavour and Fragrance Journal
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Essential oil composition ofArtemisia parvi?ora aerial parts

2003

The chemical composition of the essential oil from aerial parts of A. parviflora was analysed by GC and GC–MS. Twenty-two compounds, accounting for 72.7% of the oil, were identified. The main components identified were β-caryophyllene (15.3%), germacrene D (14.7%), camphor (11.4%), artemisia ketone (7.8%), 1,8-cineole (5.8%), α-copaene (2.6%), artemisia alcohol (2.6%), terpinene-4-ol (2.3%), caryophyllene oxide (1.2%), α-pinene (1.1%), sabinyl acetate (1.1%) and α-humulene (1.1%). Copyright © 2003 John Wiley & Sons, Ltd.

biologyTraditional medicineMonoterpeneGeneral ChemistryAsteraceaeSesquiterpenebiology.organism_classificationTerpenoidlaw.inventionchemistry.chemical_compoundCamphorchemistrylawBotanyArtemisiaChemical compositionEssential oilFood ScienceFlavour and Fragrance Journal
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Formation of Aroma by Hydrolysis of Glycosidically Bound Components

1992

SUMMARY Acid hydrolysis has been used in order to establish the presence of glycosidically bound components in fruits. During this treatment, rearrangement reactions of free monoterpene alcohols generally occur. This inconvenient may be avoided using enzymatic hydrolysis, however the specificity of enzymes requires the previous knowledge of the structures of compounds used as substrates in order to control the reaction. Several glycosidically bound components, glucosides, rutinosides and arabinoglucosides present in grapes and apricot were isolated, separated and identified using non destructive methods, MS-MS low energy CAD spectra and HPLC. s-D-glucosidase, α-L-rhamnosidase, α-L-arabinase…

chemistry.chemical_classification0303 health sciencesbiologyChemistry[SDV]Life Sciences [q-bio]Monoterpene010401 analytical chemistrySubstrate (chemistry)biology.organism_classification01 natural sciences0104 chemical sciences[SDV] Life Sciences [q-bio]03 medical and health sciencesHydrolysisEnzymeEnzymatic hydrolysisOrganic chemistryAcid hydrolysisNaringinaseComputingMilieux_MISCELLANEOUSAroma030304 developmental biology
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Suppression of new particle formation from monoterpene oxidation by NO<sub>x</sub>

2014

Abstract. The impact of nitrogen oxides (NOx = NO + NO2) on new particle formation (NPF) and on photochemical ozone production from real plant volatile organic compound (BVOC) emissions was studied in a laboratory setup. At high NOx conditions ([BVOC] / [NOx] < 7, [NOx] > 23 ppb) new particle formation was suppressed. Instead, photochemical ozone formation was observed resulting in higher hydroxyl radical (OH) and lower nitrogen monoxide (NO) concentrations. When [NO] was reduced back to levels below 1 ppb by OH reactions, NPF was observed. Adding high amounts of NOx caused NPF to be slowed by orders of magnitude compared to analogous experiments at low NOx conditions ([NOx] ~300 ppt)…

chemistry.chemical_classificationAtmospheric Science010504 meteorology & atmospheric sciencesMonoterpeneRadicalPhotodissociation010501 environmental sciencesRate-determining stepPhotochemistry01 natural sciencesOrganic compoundchemistry.chemical_compoundchemistry13. Climate actionParticleHydroxyl radicalNOx0105 earth and related environmental sciencesAtmospheric Chemistry and Physics
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Total synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone

1992

Abstract The first total stereodirected synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone from the same chiral starting product is described. A stereoselective, radical-mediated ring closure was the key step in both syntheses.

chemistry.chemical_classificationBicyclic moleculeChemistryMonoterpeneOrganic ChemistryTotal synthesisRing (chemistry)BiochemistryIsomintlactoneDrug DiscoveryOrganic chemistryStereoselectivityMINTLACTONELactoneTetrahedron
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