1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT
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1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT
1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT
1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT
Thermo Scientific Chemicals

1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT

CAS: 592-57-4 | C6H8 | 80.13 g/mol
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Catalog NumberQuantity
ALFA19394.1425 g
Catalog number ALFA19394.14
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Quantity:
25 g
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Specifications
Chemical Name or Material1,3-Cyclohexadiene
Name Notestabilized with 0.1% BHT
CAS592-57-4
Health Hazard 1H225-H335
Health Hazard 2GHS H Statement
H225
Highly flammable liquid and vapour.
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1,3-Cyclohexadiene is used as a hydrogen donor in transfer hydrogenation. It is used in the conversion to benzene. It is useful in the study of proteomics research.

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
1,3-Cyclohexadiene is used as a hydrogen donor in transfer hydrogenation. It is used in the conversion to benzene. It is useful in the study of proteomics research.

Solubility
Slightly miscible with methanol. Immiscible with water.

Notes
Incompatible with strong oxidizing agents. Store in a cool place.
RUO – Research Use Only

General References:

  1. Ohta, A.; Kobayashi, O.; Danielache, S. O.; Nanbu, S. Nonadiabatic ab initio molecular dynamics of photoisomerization reaction between 1, 3-cyclohexadiene and 1, 3, 5-cis-hexatriene. Chem. Phys. 2015, 459, 45-53.
  2. Adachi, S.; Sato, M.; Suzuki, T. Direct Observation of Ground-State Product Formation in a 1,3-Cyclohexadiene Ring-Opening Reaction. J. Phys. Chem. Lett. 2015, 6 (3), 343-346.