1,8-Cineole, 99%
1,8-Cineole, 99%
1,8-Cineole, 99%
Thermo Scientific Chemicals

1,8-Cineole, 99%

CAS: 470-82-6 | C10H18O | 154.25 g/mol
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500 mL
Catalog number A12269.AP
also known as A12269-AP
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Quantity:
500 mL
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Price (USD)
120.65
Online Exclusive
134.00
Save 13.35 (10%)
Each
Chemical Identifiers
CAS470-82-6
IUPAC Name1,3,3-trimethyl-2-oxabicyclo[2.2.2]octane
Molecular FormulaC10H18O
InChI KeyWEEGYLXZBRQIMU-UHFFFAOYSA-N
SMILESCC12CCC(CC1)C(C)(C)O2
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless
Assay (GC)≥98.5%
Refractive Index1.4560-1.4590 @ 20?C
Eucalyptol is an ingredient in many brands of mouthwash and cough suppressant. It controls airway mucus hypersecretion and asthma via anti-inflammatory cytokine inhibition. Eucalyptol is an effective treatment for nonpurulent rhinosinusitis. Eucalyptol reduces inflammation and pain when applied topically. It kills leukaemia cells in vitro.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Eucalyptol is an ingredient in many brands of mouthwash and cough suppressant. It controls airway mucus hypersecretion and asthma via anti-inflammatory cytokine inhibition. Eucalyptol is an effective treatment for nonpurulent rhinosinusitis. Eucalyptol reduces inflammation and pain when applied topically. It kills leukaemia cells in vitro.

Solubility
Soluble in water(3500 mg/L (at 21°C). Miscible with ether, alcohol, chloroform, glacial acetic acid, oils. Soluble in ethanol, ethyl ether; slightly soluble in carbon tetrachloride.

Notes
Store this chemical under refrigerated temperatures and away from mineral acids and bases. Store in a tightly closed container. Store in a dry, well-ventilated area.
RUO – Research Use Only

General References:

  1. Enio J. Leão Lanaa,; Kelly A. da Silva Rochaa,; Ivan V. Kozhevnikovb,; Elena V. Gusevskaya.Synthesis of 1,8-cineole and 1,4-cineole by isomerization of α-terpineol catalyzed by heteropoly acid. Journal of Molecular Catalysis A: Chemical. 2006, 259 (1-2)99-102.
  2. Rodney Croteau,; Frank Karp. Biosynthesis of monoterpenes: Partial purification and characterization of 1,8-cineole synthetase from Salvia officinalis . Archives of Biochemistry and Biophysics. 1977, 179(1), 257-265.