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1,4-Cyclohexadiene, 97% stab. with 0.1% BHT, Thermo Scientific Chemicals
Catalog number: L07337.06
5 g, Each
Thermo Scientific Chemicals
1,4-Cyclohexadiene, 97% stab. with 0.1% BHT, Thermo Scientific Chemicals
Catalog number: L07337.06
5 g, Each
Quantity
Catalog number: L07337.06
also known as L07337-06
Price (USD)
Price: 44.70
Online price: 37.65
Your price:
Quantity
-
Chemical Identifiers
CAS
628-41-1
Specifications
Specification SheetAppearance (Color)
Clear colorless
Identification (FTIR)
Conforms
Comment
Material sourced in the U.S. and in other countries
Refractive Index
1.4710-1.4760 @20°C (non-U.S. sourced material)
Assay (GC)
≥96.0%
Description
1,4-Cyclohexadiene is used to study the formation of parent ion from heavy fragmentation on irradiation with a high-intensity laser pulse. It is also used as a very effective hydrogen donor for catalytic hydrogenation reaction. It forms benzene at elevated temperatures in the presence of a ruthenium(II)-triphenylphosphine catalyst.
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
1,4-Cyclohexadiene is used to study the formation of parent ion from heavy fragmentation on irradiation with a high-intensity laser pulse. It is also used as a very effective hydrogen donor for catalytic hydrogenation reaction. It forms benzene at elevated temperatures in the presence of a ruthenium(II)-triphenylphosphine catalyst.
Solubility
Miscible with organic solvents like diethyl ether, tetrahydrofuran and toluene.Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
1,4-Cyclohexadiene is used to study the formation of parent ion from heavy fragmentation on irradiation with a high-intensity laser pulse. It is also used as a very effective hydrogen donor for catalytic hydrogenation reaction. It forms benzene at elevated temperatures in the presence of a ruthenium(II)-triphenylphosphine catalyst.
Solubility
Miscible with organic solvents like diethyl ether, tetrahydrofuran and toluene.Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
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