Weight | 162.019 g/mol |
---|---|
Formula | C6H5Cl2N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
3,4-DICHLOROANILINE (95-76-1)
Score:
#832 in Biology
,
#920 in Chemistry
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- Degradation of 4-Chlorophenol, 3,4-Dichloroaniline, and 2,4,6-Trinitrotoluene in an Electrohydraulic Discharge Reactor (Environmental Science & Technology, 1996)
- A comparative study of the toxicity of 1,1,2-trichloroethane, dieldrin, pentachlorophenol and 3,4 dichloroaniline for marine and fresh water organisms (Chemosphere, 1981)
- Hydrolyzable and nonhydrolyzable 3,4-dichloroaniline-humus complexes and their respective rates of biodegradation. (Journal of Agricultural and Food Chemistry, 1976)
- Metabolism of 3,4-dichloroaniline by Pseudomonas putida (Journal of Agricultural and Food Chemistry, 1982)
- Isolation of a glucosyltransferase from Arabidopsis thaliana active in the metabolism of the persistent pollutant 3,4dichloroaniline (Plant Journal, 2003)
- Enzyme-mediated coupling of 3,4-dichloroaniline and ferulic acid: a model for pollutant binding to humic materials. (Environmental Science & Technology, 1994)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H301: Toxic if swallowed
Danger Acute toxicity, oral - Category 3 - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 - H331: Toxic if inhaled
Danger Acute toxicity, inhalation - Category 3 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC1=CC(=C(C=C1N)Cl)Cl
-
InChIKeySDYWXFYBZPNOFX-UHFFFAOYSA-N
- Pubchem - 3,4-DICHLOROANILINE
- Wikipedia - 3,4-dichloroaniline
Dichloroanilines are chemical compounds which consist of an aniline ring substituted with two chlorine atoms and have the molecular formula C6H5Cl2N. There are six isomers, varying in the positions of the chlorine atoms around the ring relative to the amino group. As aniline derivatives, they are named with the amino group in position 1.
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