| Weight | 163.003 g/mol |
|---|---|
| Formula | C6H4Cl2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,5-dichlorophenol (583-78-8)
2,5-dichlorophenol, potassium salt · 2,5-dichlorophenol, sodium salt
Score:
#116 in Environmental science
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- Kinetic Studies in Heterogeneous Photocatalysis. 2. TiO2-mediated degradation of 4-chlorophenol alone and in a three component mixture of 4-chlorophenol, 2,4-dichlorophenol and 2,4,5-trichlorophenol in air equilibrated aqueous media (Langmuir, 1989)
- Quantification of urinary conjugates of bisphenol A, 2,5-dichlorophenol, and 2-hydroxy-4-methoxybenzophenone in humans by online solid phase extraction-high performance liquid chromatography-tandem mass spectrometry. (Analytical and Bioanalytical Chemistry, 2005)
- Monohydroxylation of phenol and 2,5-dichlorophenol by toluene dioxygenase in Pseudomonas putida F1. (Applied and Environmental Microbiology, 1989)
- 2,5-Dichlorophenol (from Ingested Herbicide?) in Defensive Secretion of Grasshopper (Science, 1971)
- Sequence analysis of the 2,4-dichlorophenol hydroxylase gene tfdB and 3,5-dichlorocatechol 1,2-dioxygenase gene tfdC of 2,4-dichlorophenoxyacetic acid degrading plasmid pEST4011 (Gene, 1996)
- Synergistic Extraction of Gallium(III) and Indium(III) with 2,4-Pentanedione and 3,5-Dichlorophenol on the Basis of Outer-Sphere Complexation (Analytical Sciences, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 - 2,5-dichlorophenol, potassium salt
- 2,5-dichlorophenol, sodium salt
-
SMILESC1=CC(=C(C=C1Cl)O)Cl
-
InChIKeyRANCECPPZPIPNO-UHFFFAOYSA-N
- Pubchem - 2,5-dichlorophenol
- Wikipedia - 2,5-dichlorophenol
Dichlorophenols (DCPs) are any of several chemical compounds which are derivatives of phenol containing two chlorine atoms. There are six isomers: 2,3-Dichlorophenol 2,4-Dichlorophenol 2,5-Dichlorophenol 2,6-Dichlorophenol 3,4-Dichlorophenol 3,5-Dichlorophenol Dichlorophenols are used as intermediates in the manufacture of more complex chemical compounds, including the common herbicide 2,4-dichlorophenoxyacetic acid (2,4-D).
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