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CARVEOL

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CARVEOL Basic information
  • Product Name:CARVEOL
  • CAS:99-48-9
  • MF:C10H16O
  • MW:152.23
  • EINECS:202-757-4
  • Mol File:99-48-9.mol
CARVEOL Chemical Properties
  • Melting point:24-25 °C
  • Boiling point:226-227 °C751 mm Hg(lit.)
  • Density 0.958 g/mL at 25 °C(lit.)
  • refractive index n20/D 1.496
  • FEMA 2247 | CARVEOL
  • Flash point:209 °F
  • storage temp. 2-8°C
  • pka14.60±0.60(Predicted)
  • form neat
  • Specific Gravity0.96
  • optical activity[α]22/D 115°, c = 1 in chloroform
  • Water Solubility Partly soluble in water. Soluble in alcohol, ethanol and DMSO.
  • JECFA Number381
  • BRN 6269416
  • EPA Substance Registry SystemCarveol (99-48-9)
Safety Information
  • Hazard Codes Xi
  • Risk Statements 36/37/38
  • Safety Statements 26-37/39
  • WGK Germany 2
  • RTECS OS8400000
  • TSCA Yes
  • HS Code 29061900
MSDS
  • Language:EnglishProvider:ACROS
CARVEOL Usage And Synthesis
  • Chemical PropertiesClear colorless to slightly yellow liquid
  • Chemical PropertiesCarveol has spearmint-like odor.
  • OccurrenceIn small amounts, sometimes esterified, it has been reported present in caraway seeds, spearmint, orange juice, mango and eucalyptus oil.
  • DefinitionChEBI: A limonene monoterpenoid that is cyclohex-2-en-1-ol substituted by a methyl group at position 2 and a prop-1-en-2-yl group at position 5.
  • Aroma threshold valuesDetection: 4 ppm
  • General DescriptionClear colorless liquid. Insoluble in water.
  • Air & Water ReactionsInsoluble in water.
  • Reactivity ProfileFlammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.
  • Health HazardACUTE/CHRONIC HAZARDS: Toxic.
  • Chemical SynthesisThe various d-, l- and dl- (cis- and trans-, respectively) forms have been prepared synthetically and isolated by means of the dinitrobenzoates according to Amvers’ law. They are prepared by oxidation of limonene or, better, from carvone.
CARVEOL Preparation Products And Raw materials
CARVEOL(99-48-9)Related Product Information
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