| Weight | 126.111 g/mol |
|---|---|
| Formula | C6H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1,2,4-BENZENETRIOL (533-73-3)
hydroxyhydroquinone · hydroxyquinol · 1,2,4-trihydroxybenzene
Score:
#2455 in Biochemistry
,
#4813 in Biology
,
#6144 in Chemistry
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LabBot
- Biodegradation of p-nitrophenol via 1,2,4-benzenetriol by an Arthrobacter sp. (Applied and Environmental Microbiology, 1994)
- Hydrothermal formation of 1,2,4-benzenetriol from 5-hydroxymethyl-2-furaldehyde and D-fructose (Carbohydrate Research, 1993)
- Novel 4-chlorophenol degradation gene cluster and degradation route via hydroxyquinol in Arthrobacter chlorophenolicus A6. (Applied and Environmental Microbiology, 2005)
- Benzene metabolite, 1,2,4-benzenetriol, induces micronuclei and oxidative DNA damage in human lymphocytes and HL60 cells (Environmental and Molecular Mutagenesis, 1993)
- Purification of hydroxyquinol 1,2-dioxygenase and maleylacetate reductase: the lower pathway of 2,4,5-trichlorophenoxyacetic acid metabolism by Burkholderia cepacia AC1100. (Applied and Environmental Microbiology, 1996)
- Human DNA Damage Induced by 1,2,4-Benzenetriol, a Benzene Metabolite (Cancer Research, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - hydroxyhydroquinone
- hydroxyquinol
- 1,2,4-trihydroxybenzene
-
SMILESC1=CC(=C(C=C1O)O)O
-
InChIKeyGGNQRNBDZQJCCN-UHFFFAOYSA-N
- Pubchem - 1,2,4-BENZENETRIOL
- Wikipedia - 1,2,4-trihydroxybenzene
Hydroxyquinol is an organic compound with the formula C6H3(OH)3. It is one of three isomeric benzenetriols. The compound is a colorless solid that is soluble in water.
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