Cyclooctane, 99+%, Thermo Scientific Chemicals
Cyclooctane, 99+%, Thermo Scientific Chemicals
Cyclooctane, 99+%, Thermo Scientific Chemicals
Cyclooctane, 99+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Cyclooctane, 99+%, Thermo Scientific Chemicals

CAS: 292-64-8 | C8H16 | 112.216 g/mol
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Catalog NumberQuantity
ALFL15000.AD50 mL
Catalog number ALFL15000.AD
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50 mL
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Specifications
Chemical Name or MaterialCyclooctane
CAS292-64-8
Health Hazard 1H226-H304
Health Hazard 2GHS H Statement
H304-H226
May be fatal if swallowed and enters airways.
Flammable liquid and vapor.
Health Hazard 3P210-P233-P240-P241-P242-P243-P280-P301+P310-P303+P361+P353-P331-P370+P378q-P501c
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Cyclooctane is used as solvent, reagents and synthetic organic intermediates and it can be used to produce cyclooctanone. It is also used as an intermediate in production of plastics, fibers, adhesives and coatings.

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
Cyclooctane is used as solvent, reagents and synthetic organic intermediates and it can be used to produce cyclooctanone. It is also used as an intermediate in production of plastics, fibers, adhesives and coatings.

Solubility
Not miscible or difficult to mix in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Gerald K. Cook.; James M. Mayer. C-H Bond Activation by Metal Oxo Species: Chromyl Chloride Oxidations of Cyclooctane, Isobutane, and Toluene. J. Am. Chem. Soc. 1995, 117 (27), 7139-7156.
  2. F. A. L. Anet.; V. J. Basus. Detection of a crown family conformation in cyclooctane by proton and carbon-13 nuclear magnetic resonance. J. Am. Chem. Soc. 1973, 95 (13), 4424-4426.