p-Cymene - Wikipedia
p-Cymene is a naturally occurring aromatic organic compound. It is classified as an alkylbenzene related to monocyclic monoterpenes. [3] Its structure consists of a benzene ring para-substituted with a methyl group and an isopropyl group. p-Cymene is insoluble in water, but miscible with organic solvents.
p-Cymene - NIST Chemistry WebBook
2010年5月7日 · p-Cymene. Formula: C 10 H 14. Molecular weight: 134.2182. IUPAC Standard InChI: InChI=1S/C10H14/c1-8 (2)10-6-4-9 (3)5-7-10/h4-8H,1-3H3. IUPAC Standard InChIKey: HFPZCAJZSCWRBC-UHFFFAOYSA-N. CAS Registry Number: 99-87-6. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file.
p-Cymene - NIST Chemistry WebBook
Column type Active phase Temperature (C) I Reference Comment; Capillary: PEG-20M: 70. 1268.8: Tóth, 1983: N2; Column length: 30. m; Column diameter: 0.3 mm: Capillary
Cymene - Wikipedia
Cymene. Cymene describes organic compounds with the formula CH3C6H4CH (CH3)2. Three isomers exist: 1,2- 1,3-, and 1,4-. All are colorless liquids, immiscible in water, with similar boiling points. They are classified are aromatic hydrocarbons.
Health beneficial and pharmacological properties of p-cymene
p-cymene also known as p-cymol or p-isopropyltoluene is an alkyl-substituted aromatic compound naturally occurring in essential oils (EOs) of various aromatic plants, including the genus of Artemisia, Protium, Origanum, and Thymus.
p-CYMENE | C10H14 | CID 7463 - PubChem
p-CYMENE | C10H14 | CID 7463 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
Update on Monoterpenes as Antimicrobial Agents: A Particular ...
p-Cymene [1-methyl-4-(1-methylethyl)-benzene] is a monoterpene found in over 100 plant species used for medicine and food purposes. It shows a range of biological activity including antioxidant, anti-inflammatory, antinociceptive, anxiolytic, anticancer and antimicrobial effects.
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