| Weight | 293.414 g/mol |
|---|---|
| Formula | C19H23N3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
AMITRAZ (33089-61-1)
Mitaban · U 36059 · Taktic
Score:
#714 in Biology
,
#771 in Chemistry
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- Detection and Characterization of Amitraz Resistance in the Southern Cattle Tick, Boophilus microplus (Acari: Ixodidae) (Journal of Medical Entomology, 2004)
- Control of Varroa jacobsoni Oud. resistant to fluvalinate and amitraz using coumaphos. (Apidologie, 2000)
- Effect of amitraz and chlordimeform on heart rate and pupil diameter in rats: Mediated by 2-adrenoreceptors (Toxicology and Applied Pharmacology, 1984)
- Effects of amitraz, several opiate derivatives and anticholinergic agents on intestinal transit in ponies (Equine Veterinary Journal, 1986)
- MODIFICATION OF MTT ASSAY CONDITIONS TO EXAMINE THE CYTOTOXIC EFFECTS OF AMITRAZ ON THE HUMAN LYMPHOBLASTOID CELL LINE, WIL2NS (Toxicology in Vitro, 2005)
- Diagnosis of amitraz resistance in Boophilus microplus in New Caledonia with the modified Larval Packet Test (Veterinary Parasitology, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H371: May cause damage to organs
Warning Specific target organ toxicity, single exposure - Category 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - Mitaban
- U 36059
- Taktic
- N-methyl-bis(2,4-xylyiminomethyl) amine
-
SMILESCC1=CC(=C(C=C1)N=CN(C)C=NC2=C(C=C(C=C2)C)C)C
-
InChIKeyQXAITBQSYVNQDR-UHFFFAOYSA-N
- Pubchem - AMITRAZ
- Wikipedia - amitraz
Amitraz (development code BTS27419) is a non-systemic acaricide and insecticide and has also been described as a scabicide. It was first synthesized by the Boots Co. in England in 1969.
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Estimated Properties
| Density | 1 g/cm3 | EPA T.E.S.T. |
|---|---|---|
| Flash Point | 181.24 C | EPA T.E.S.T. |
| Water Solubility | 9.71 mg/L | EPA T.E.S.T. |
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