Weight | 196.681 g/mol |
---|---|
Formula | C10H13ClN2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
CHLORDIMEFORM (6164-98-3)
Chlorphenamidine
Score:
#1121 in Biology
,
#1266 in Chemistry
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- Comparison of chlordimeform and carbaryl using a functional observational battery (Toxicological Sciences, 1988)
- Inhibition of Monoamine Oxidase by the Pesticide Chlordimeform and Related Compounds (Nature, 1973)
- Chlordimeform: a pesticide acting upon amine regulatory mechanisms. (Nature, 1973)
- Effect of amitraz and chlordimeform on heart rate and pupil diameter in rats: Mediated by 2-adrenoreceptors (Toxicology and Applied Pharmacology, 1984)
- Biochemical and physiological effects of chlordimeform. (Environmental Health Perspectives, 1976)
- Octopamine and chlordimeform enhance sensory responsiveness and production of the flight motor pattern in developing and adult moths (Journal of Neurobiology, 1984)
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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 - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H316: Causes mild skin irritation
Warning Skin corrosion/irritation - Category 3 - H332: Harmful if inhaled
Warning Acute toxicity, inhalation - Category 4 - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - 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 - Chlorphenamidine
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SMILESCC1=C(C=CC(=C1)Cl)N=CN(C)C
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InChIKeySTUSTWKEFDQFFZ-UHFFFAOYSA-N
- Pubchem - CHLORDIMEFORM
- Wikipedia - Chlordimeform
Chlordimeform is an acaricide (pesticide) active mainly against motile forms of mites and ticks and against eggs and early instars of some Lepidoptera insects. After the International Agency for Research on Cancer reported sufficient evidence that its major metabolite, 4-chloro-o-toluidine, was a carcinogen, its use has ceased and its registration has been withdrawn in most countries.
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