1,4-Cyclohexandion, 98 %, Thermo Scientific Chemicals
1,4-Cyclohexandion, 98 %, Thermo Scientific Chemicals
1,4-Cyclohexandion, 98 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

1,4-Cyclohexandion, 98 %, Thermo Scientific Chemicals

CAS: 637-88-7 | C6H8O2 | 112.128 g/mol
Have Questions?
Ansicht ändernbuttonViewtableView
Menge:
25 g
100 g
500 g
Katalognummer A11100.14
auch als A11100-14 bezeichnet
Preis (EUR)
64,10
Each
Menge:
25 g
Großbestellung oder individuelle Größe anfordern
Preis (EUR)
64,10
Each
Chemikalien-Kennzeichnungen
CAS637-88-7
IUPAC Namecyclohexane-1,4-dione
Molecular FormulaC6H8O2
InChI KeyDCZFGQYXRKMVFG-UHFFFAOYSA-N
SMILESO=C1CCC(=O)CC1
Mehr anzeigen
SpecificationsSpecification SheetDatenblatt
Melting 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.

Anwendungen
1,4-Cyclohexandion wird bei der Herstellung von 1,4-Benzochinon und Bromorganika verwendet. Wird auch zur Untersuchung des Einflusses von sichtbarem Licht auf die Bromat-1,4-Cyclohexandione-Ferroin-oszillierende Reaktion verwendet. Spielt eine wichtige Rolle für Pharmazeutika, Pflanzenwachstumsregulatoren und als leitfähiges Material.

Löslichkeit
Löslich in Methanol und Ethanol.

Hinweise
Nicht kompatibel mit starken Oxidationsmitteln.
RUO – Research Use Only

Allgemeine Referenzen:

  1. 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.
  2. 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.
  3. 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.
  4. 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.
  5. 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.