Anthraquinone (90530-46-4, 84-65-1)

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  100 g
  $66.00

  1 Kg
  $182.00

Most-cited Publications

• Hydrogen Peroxide Synthesis: An Outlook beyond the Anthraquinone Process (Angewandte Chemie, 2006)
• Structural characterization of technical lignins for the production of adhesives: Application to lignosulfonate, kraft, soda-anthraquinone, organosolv and ethanol process lignins (Industrial Crops and Products, 2006)
• Antifungal activity of anthraquinone derivatives from Rheum emodi (Journal of Ethnopharmacology, 2000)
• Anthraquinone-Based Intramolecular Charge-Transfer Compounds: Computational Molecular Design, Thermally Activated Delayed Fluorescence, and Highly Efficient Red Electroluminescence (Journal of the American Chemical Society, 2014)
• Anthraquinone based polymer as high performance cathode material for rechargeable lithium batteries (Chemical Communications, 2009)
• ANTHRAQUINONE PRODUCTION BY CELL SUSPENSION CULTURES OF MORINDA CITRIFOLIA (Planta Medica, 1975)

Areas of Application

Safety

• Request a Demo
  Predict GHS Hazards for Any Chemical in silico.
  Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.
• H320: Causes eye irritation
  Warning Serious eye damage/eye irritation - Category 2B
• H373: Causes damage to organs through prolonged or repeated exposure
  Warning Specific target organ toxicity, repeated exposure - Category 2
• H410: Very toxic to aquatic life with long lasting effects
  Warning Hazardous to the aquatic environment, long-term hazard - Category 1

Trends

Alternate Names

• 9,10-anthraquinone
• 9,10-anthracenedione
• 9,10-anthraquinone, radical ion (1-)
• SMILES
  C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O
• InChIKey
  RZVHIXYEVGDQDX-UHFFFAOYSA-N

External Links

• Pubchem - Anthraquinone
• Wikipedia - anthraquinone
  Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with formula C 14H 8O 2. Several isomers are possible, each of which can be viewed as a quinone derivative. The term anthraquinone, however, almost invariably refers to one specific isomer, 9,10-anthraquinone (IUPAC: 9,10-dioxoanthracene) wherein the keto groups are located on the central ring.

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Anthraquinone

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