| Weight | 172.092 g/mol |
|---|---|
| Formula | C6H4O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
tetroquinone (319-89-1, 5676-48-2)
tetrahydroxy-1,4-quinone
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- Mechanism of tetrahydroxy-1,4-quinone cytotoxicity: Involvement of Ca22+ and H2O2 in the impairment of DNA replication and mitochondrial function (Free Radical Biology and Medicine, 1996)
- Study of the Interaction Between Technetium and Tetrahydroxy-1,4-Quinone (Radiochimica Acta, 1986)
- Ultraviolet Absorption Spectra, Solvent Effect and Non-Linear Optical Properties of Tetrahydroxy-1,4-quinone Hydrate by Hartee-Fock and Density Functional Theory (Asian Journal of Chemistry, 2017)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tetrahydroxy-1,4-quinone
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SMILESC1(=C(C(=O)C(=C(C1=O)O)O)O)O
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InChIKeyDGQOCLATAPFASR-UHFFFAOYSA-N
- Pubchem - tetroquinone
- Wikipedia - tetroquinone
Tetrahydroxy-1,4-benzoquinone, also called tetrahydroxy-p-benzoquinone, tetrahydroxybenzoquinone, or tetrahydroxyquinone (THBQ, THQ), is an organic compound with formula C6O2(OH)4. Its molecular structure consists of a cyclohexadiene ring with four hydroxyl groups and two ketone groups in opposite (para) positions. The compound gives a light red solution in water, and crystallizes as the glistening bluish-black (but non-conducting) dihydrate C6O2(OH)42H2O.
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tetroquinone
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