Identification | More | [Name]
Azocyclotin | [CAS]
41083-11-8 | [Synonyms]
1-(TRICYCLOHEXYL-STANNYL)-1H-1,2,4-TRIAZOLE AZOCYCLOTIN CLAIRMAIT(R) CLERMAIT(R) PEROPAL PEROPAL(R) (1h-1,2,4-triazol-1-yl)tricyclohexyl-stannan (1h-1,2,4-triazolyl)tricyclohexylstannane 2,4-Triazole,1-(tricyclohexylstannyl)-1H-1 baybue1452 tri(cyklohexyl)-1h-1,2,4-triazol-1-ylstannium Triclotin AZOCYCLOTIN PESTANAL (1-(TRICYCLO-HEXYL AZOCYCLOTIN, 250MG, NEAT Tricyclotin 1H-1,2,4-Triazole, 1-(tricyclohexylstannyl)- azocyclotin (bsi,iso,esa) AZOCYCLOTIN STANDARD 1-(tricyclohexylstannyl)-1H-1,2,4-triazole azocyclotin Clermait | [EINECS(EC#)]
255-209-1 | [Molecular Formula]
C20H35N3Sn | [MDL Number]
MFCD00055290 | [Molecular Weight]
436.22 | [MOL File]
41083-11-8.mol |
Safety Data | Back Directory | [Hazard Codes ]
T+;N,N,T+ | [Risk Statements ]
R25:Toxic if swallowed. R26:Very Toxic by inhalation. R37/38:Irritating to respiratory system and skin . R41:Risk of serious damage to eyes. R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S38:In case of insufficient ventilation, wear suitable respiratory equipment . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S60:This material and/or its container must be disposed of as hazardous waste . S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
UN 2786 | [WGK Germany ]
3 | [RTECS ]
WH8637700 | [HazardClass ]
6.1(a) | [PackingGroup ]
I | [Hazardous Substances Data]
41083-11-8(Hazardous Substances Data) |
Hazard Information | Back Directory | [Uses]
Azocyclotin is an organotin aracacide used in the control of mites. Azocyclotin showed weak antifeedant activity against other insects such as Spodoptera littoralis. | [Uses]
Azocyclotin is used to control all motile stages of spider mites on
fruit, vines, hops, cotton, vegetables and ornamentals. | [Definition]
ChEBI: A member of the class of triazoles that is 1,2,4-triazole substituted at position 1 by a tricyclohexylstannyl group. | [Metabolic pathway]
The sedimentation of particles coated with the
pesticide is relatively fast. Shortly after application of
14C-azocyclotin, distribution, solubilizing, and
metabolism in fresh water microcosms begin, and
azocyclotin is quickly hydrolyzed to cyhexatin
(tricyclohexyltin hydroxide) by splitting of the triazole
residue, and, according to the solubility of cyhexatin,
cyhexatin is mainly absorbed to sediment and the
layer of biota in direct contact with the sediment and
further undergoes successive metabolism to result in
dicyclohexyltin oxide and cyclohexyltin acid. | [Degradation]
Azocyclotin undergoes hydrolysis with DT50 values (22 °C) of 96 hours at
pH 4,81 hours at pH 7 and 8 hours at pH 9 (I'M). |
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