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

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

CAS: 470-82-6 | C10H18O | 154.25 g/mol
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Catalog NumberQuantity
ALFA12269.AE100 mL
Catalog number ALFA12269.AE
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100 mL
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Specifications
Chemical Name or MaterialCineole
CAS470-82-6
Health Hazard 1H226-H315-H319
Health Hazard 2GHS H Statement
H226
Health Hazard 3P210-P233-P240-P241-P242-P243-P264b-P280-P303+P361+P353-P305+P351+P338-P332+P313-P363-P370+P378q-P501c
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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.