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1,4-Cyclohexanedione, 98%, Thermo Scientific Chemicals
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Catalog number A11100.36
also known as A11100-36
Price (USD)/ Each
905.00
-
Quantity:
500 g
Price (USD)/ Each
905.00
1,4-Cyclohexanedione, 98%, Thermo Scientific Chemicals
Catalog numberA11100.36
Price (USD)/ Each
905.00
-
Chemical Identifiers
CAS637-88-7
IUPAC Namecyclohexane-1,4-dione
Molecular FormulaC6H8O2
InChI KeyDCZFGQYXRKMVFG-UHFFFAOYSA-N
SMILESO=C1CCC(=O)CC1
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Specifications
Specification Sheet
Specification SheetMelting Point (clear melt)74.5-80.5?C
FormCrystals or powder or crystalline powder
Appearance (Color)Pale yellow to yellow or pale cream to pale brown
Assay (GC)≥97.5%
1,4-Cyclohexanedione is used in the preparation of 1,4 benzoquinone and bromoorganics. It is also used to study the influence of visible light on the bromate-1,4-cyclohexanedione-ferroin oscillating reaction. It plays a vital role in pharmaceuticals, plant growth regulator and as a conducting material.
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-Cyclohexanedione is used in the preparation of 1,4 benzoquinone and bromoorganics. It is also used to study the influence of visible light on the bromate-1,4-cyclohexanedione-ferroin oscillating reaction. It plays a vital role in pharmaceuticals, plant growth regulator and as a conducting material.
Solubility
Soluble in methanol and ethanol.
Notes
Incompatible with strong oxidizing agents.
1,4-Cyclohexanedione is used in the preparation of 1,4 benzoquinone and bromoorganics. It is also used to study the influence of visible light on the bromate-1,4-cyclohexanedione-ferroin oscillating reaction. It plays a vital role in pharmaceuticals, plant growth regulator and as a conducting material.
Solubility
Soluble in methanol and ethanol.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Miyazato, H.; Nakamura, M.; Hashimoto, S.; Hayashi, S. Identification of the odour-active cyclic diketone cis-2,6-dimethyl-1,4-cyclohexanedione in roasted Arabica coffee brew. Food Chem. 2013, 138(4), 2346-2355.
- Li, J.; Wang, J. Complex Dynamical Behavior in the Highly Photosensitive Cerium-Bromate-1,4-Benzoquinone Reaction. J. Phys. Chem. A 2012, 116 (31), 8130-8137.
- Chen, Z.; Yang, W.; Hu, Y-H.; Lei, Z-Y.; Wang, Y-H.; Wan, W-Q. Measurement and Correlation for the Solubility of Dimethyl 1,4-Cyclohexanedione-2,5-dicarboxylate in Different Solvents at Temperatures from (278.15 to 323.15) K. J. Chem. Eng. Data 2011, 56 (5), 2726-2729.
- Bell, J. G.; Wang, J. Complex Spatiotemporal Behavior in the Photosensitive Ferroin-Bromate-4-Nitrophenol Reaction. J. Phys. Chem. A 2015, 119 (14), 3323-3328.
- Budroni, M. A.; Rossi, F. A Novel Mechanism for in Situ Nucleation of Spirals Controlled by the Interplay between Phase Fronts and Reaction-Diffusion Waves in an Oscillatory Medium. J. Phys. Chem. C 2015, 119 (17), 9411-9417.