| Identification | Back Directory | [Name]
BENZTHIAZURON | [CAS]
1929-88-0 | [Synonyms]
gatnon
s22012
gatinon
B-60618
bay60618
GATNON(R)
Bayer 60618
Benthiazuron
BENZTHIAZURON
Benzthiazuron-D3
Benzthiazuron (95%)
Benzthiazuron Solution
benzthiazuron (bsi,iso)
2 6-DICHLOROANISOLE PESTANAL
2-(1-methylureido)-benzothiazol
1-methyl-3-(2-benzthiazolyl)urea
1-benzothiazol-2-yl-3-methylurea
1-(2-BENZOTHIAZOLYL)-3-METHYLUREA
1-(2-benzothiazolyl)-3-methyl-ure
1-Methyl-3-(2-benzothiazolyl)urea
n-(2-benzothiazolyl)-n’-methylurea
3-(2-benzthiazolyl)-1-methylharnstoff
n-(2-benzthiazolyl)-n’-methylharnstoff
1-(1,3-BENZOTHIAZOL-2-YL)-3-METHYLUREA
Benzthiazuron(100ug/mlinMethylenechloride)
benzthiazuron (ISO) 1-benzothiazol-2-yl-3-methylurea | [EINECS(EC#)]
217-685-9 | [Molecular Formula]
C9H9N3OS | [MDL Number]
MFCD00055363 | [MOL File]
1929-88-0.mol | [Molecular Weight]
207.25 |
| Hazard Information | Back Directory | [Description]
Benzthiazuron is an obsolete pre-emergence herbicide that was used mainly to control annual broadleaved weeds in a variety of crops. This herbicide has a moderate aqueous solubility and is not volatile. There is some evidence that it can be moderately persistent in some soil systems. Based on its physico-chemical properties benzthiazuron also has potential to leach to groundwaters. Ecotoxicology information is scant but for aquatic organisms the risk appears to be low to moderate. The mammalian oral toxicity is moderate and the substance is a skin and eye irritant. | [Uses]
Benzthiazuron is an herbicide. It is generally a component of pesticide compositions. | [Definition]
ChEBI: Benzthiazuron is a member of benzothiazoles. | [Production Methods]
The commercial production of benzthiazuron begins with the preparation of 2-aminobenzothiazole, obtained by reacting aniline with sulphur and carbon disulfide in a high-pressure autoclave (the Hugerschoff reaction variant), or more commonly in modern plants via cyclisation of phenylthiourea using bromine in acetic acid, followed by neutralisation and crystallisation to yield the heterocyclic amine. This intermediate is then reacted with methyl isocyanate in an inert solvent such as toluene or acetone, where the nucleophilic amine attacks the isocyanate to form the unsymmetrical urea linkage. The resulting benzthiazuron precipitates upon cooling. | [Mechanism of action]
Absorbed by roots and translocated. PSII inhibitor resulting in plant cell death and plant necrosis. | [Pesticide Type]
Herbicide |
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| Company Name: |
TOSUN PHARM
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| Tel: |
020-66392521-118 18922260391 |
| Website: |
www.toref.cn/ |
| Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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