Methabenzthiazuron
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Methabenzthiazuron
structure -
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CAS No:
18691-97-9
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Formula:
C10H11N3OS
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Chemical Name:
Methabenzthiazuron
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Synonyms:
Urea,N-2-benzothiazolyl-N,N′-dimethyl-;Urea,1-(2-benzothiazolyl)-1,3-dimethyl-;N-2-Benzothiazolyl-N,N′-dimethylurea;1-(2-Benzothiazolyl)-1,3-dimethylurea;Methabenzthiazuron;Methbenzthiazuron;Preparation 5633;Tribunil;5633;Bayer 5653;Metabenzthiazuron;Bayer 74283;BAY 5653;1,3-Dimethyl-3-(2-benzothiazolyl)urea;Methibenzuron
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CAS No:
Description
White crystalline solid; melts at 120°C(248°F); insoluble in water [~59 ppm at20°C (68°F)], soluble in organic solvents.
Methabenzthiazuron is a member of benzothiazoles.
Characteristics
73.5
1.63
white crystalline solid
1.2527 (rough estimate)
120 °C
11 °C
1.6740 (estimate)
2.67e-04 M
APPROX 4°C
1.13e-07 mmHg
Oral-Rat LD50: 2500 mg/kg; Oral-Mouse LD50: 1000 mg/kg
Combustion produces toxic sulfur oxide and nitrogen oxide gas
142.47 Ų [M+H]+ [CCS Type: TW]|142.2 Ų [M+H]+
Safety Information
III
9
UN30779/PG3
2
50/53-39/23/24/25-23/24/25-11
60-61-45-16-7
YR8980000
N,T,F
The warehouse is ventilated, low temperature and dry; stored and transported separately from food materials
P273-P501
H410
|Warning|H400: Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]|P273, P391, and P501|Danger|H330 (42.86%): Fatal if inhaled [Danger Acute toxicity, inhalation]|P260, P271, P273, P284, P304+P340, P310, P320, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 77 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.|H410: Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]
Methabenzthiazuron Use and Manufacturing
In the presence of sodium carbonate, aniline reacts with CS2 to form sodium aniline thioformate, and then reacts with monomethylamine to prepare N-phenyl-N'-methylthiourea. Subsequent reaction with sulfuryl chloride generates 2-methylaminobenzothiazole. Finally, it reacts with methyl isocyanate to synthesize methyl benzothione. Or react 2-methylaminobenzothiazole with methylcarbamoyl chloride to produce methylbenzthione.
Selective herbicide.
Agrochemicals -> Herbicides|Herbicides
Computed Properties
Molecular Weight:221.28
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:221.06228316
Monoisotopic Mass:221.06228316
Topological Polar Surface Area:73.5
Heavy Atom Count:15
Complexity:249
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of Methabenzthiazuron
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Latest News on Methabenzthiazuron
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- 2024 Central Plains (Handan) Modern Agriculture Expo and agricultural materials trading Conference will be held in August
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