| Weight | 240.214 g/mol |
|---|---|
| Formula | C14H8O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
Quinizarin (81-64-1, 86321-26-8)
anthrarufin · 1,4-dihydroxyanthraquinone, radiacal ion (1-) · 1,4-dihydroxy-9,10-anthraquinone
Score:
#1418 in Physics
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#4164 in Chemistry
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- Spectral diffusion of a photochemical proton transfer system in an amorphous organic host: Quinizarin in alcohol glass (Journal of Chemical Physics, 1984)
- Dynamics of Interfacial Electron Transfer from Photoexcited Quinizarin (Qz) into the Conduction Band of TiO2 and Surface States of ZrO2 Nanoparticles (Journal of Physical Chemistry B, 2004)
- Metal ion binding to daunorubicin and quinizarin (Inorganica Chimica Acta, 1982)
- Intramolecular hydrogen bonding in substituted anthraquinones by laser-induced fluorescence. 1. 1,4-Dihydroxyanthraquinone (quinizarin) (The Journal of Physical Chemistry, 1982)
- Synthesis of and Fluorescent Imaging with a Polymer Having t-BOC-Protected Quinizarin Moieties (Advanced Materials, 1999)
- The Management of the Quinizarin Sweat Test (Postgraduate Medical Journal, 1947)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - anthrarufin
- 1,4-dihydroxyanthraquinone, radiacal ion (1-)
- 1,4-dihydroxy-9,10-anthraquinone
- 1,4-dihydroxyanthraquinone
-
SMILESC1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)O
-
InChIKeyGUEIZVNYDFNHJU-UHFFFAOYSA-N
- Pubchem - Quinizarin
- Wikipedia - quinizarin
1,4-Dihydroxyanthraquinone, also called quinizarin or Solvent Orange 86, is an organic compound derived from anthroquinone. Quinizarin is an orange or red-brown crystalline powder. It is formally derived from anthraquinone by replacement of two hydrogen atoms by hydroxyl (OH) groups.
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Quinizarin
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