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trans-4-Methylcyclohexanol, 98%, Thermo Scientific Chemicals
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Catalog number B20054.06
also known as B20054-06
Price (USD)/ Each
95.10
-
Quantity:
5 g
Price (USD)/ Each
95.10
trans-4-Methylcyclohexanol, 98%, Thermo Scientific Chemicals
Catalog numberB20054.06
Price (USD)/ Each
95.10
-
Chemical Identifiers
CAS7731-29-5
IUPAC Name4-methylcyclohexan-1-ol
Molecular FormulaC7H14O
InChI KeyMQWCXKGKQLNYQG-UHFFFAOYSA-N
SMILESCC1CCC(O)CC1
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Specifications
Specification Sheet
Specification SheetAssay (GC)>97.5%
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.4545-1.4580 @ 20?C
FormLiquid
trans-4-Methylcyclohexanol is used to prepare 4-methylcyclohexyl nitrite to study the laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals.
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
trans-4-Methylcyclohexanol is used to prepare 4-methylcyclohexyl nitrite to study the laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals.
Solubility
Slightly soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
trans-4-Methylcyclohexanol is used to prepare 4-methylcyclohexyl nitrite to study the laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals.
Solubility
Slightly soluble in water.
Notes
Store away from oxidizing agents. Keep the container tightly closed and place it in a cool, dry and well ventilated condition.
RUO – Research Use Only
General References:
- Lei Zhang, et al. Laser-induced fluorescence spectra of 4-methylcyclohexoxy radical and perdeuterated cyclohexoxy radical and direct kinetic studies of their reactions with O2.J. Phys. Chem. A.2005,109(41), 9232-9240.
- Miyazawa M, et al. Biological enantioselective reduction of methylcyclohexanones by Glomerella cingulata.J. Chem. Technol. Biotechnol.1996,65(2), 171-175.