|
| Product Name: | Amidosulfuron | | Synonyms: | AMIDOSULFURON;Amidosulfuron PESTANAL;GRATIL;n-(((((4,6-dimethoxy-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)-n-methylmethanesulfonamide;METHYLMETHANESULFONAMIDE;1-(4,6-Dimethoxypyrimidin-2-yl)-3-(N-mesyl-N-methylsulfamoyl)urea;Amidosulfuron [iso];3,5-Dithia-2,4-diazahexanaMide,N-(4,6-diMethoxy-2-pyriMidinyl)-4-Methyl-, 3,3,5,5-tetraoxide | | CAS: | 120923-37-7 | | MF: | C9H15N5O7S2 | | MW: | 369.37 | | EINECS: | 407-380-0 | | Product Categories: | | | Mol File: | 120923-37-7.mol |  |
| | Amidosulfuron Chemical Properties |
| Melting point | 160-163°C | | density | 1.594±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | DMSO (Slightly), Methanol (Slightly, Heated) | | pka | 0.12±0.40(Predicted) | | form | neat | | color | White to Off-White | | Stability: | Hygroscopic, Unstable in Solution | | LogP | 1.630 | | CAS DataBase Reference | 120923-37-7(CAS DataBase Reference) |
| Risk Statements | 52/53 | | Safety Statements | 61 | | WGK Germany | 1 |
| | Amidosulfuron Usage And Synthesis |
| Description | Amidosulfuron is a broad spectrum herbicide that is used to control broad-leaved weeds. It is volatile, highly soluble in water and, based on its chemical properties, has a high potential for leaching to groundwater. It is not persistent in soil systems but may be persistent in water under certain conditions. | | Toxicity | Amidosulfuron has a low mammalian toxicity and would not be expected to bioaccumulate. Amidosulfuron is moderately toxic to most terrestrial and aquatic species. | | Uses | Herbicide. | | Uses | Amidosulfuron, is used as pesticide and herbicides. | | Definition | ChEBI: Amidosulfuron is an aromatic ether. | | Metabolic pathway | The hydrolysis of 14C-amidosulfuron in buffer aqueous
solutions under various conditions results in 2-amino-
4,6-dimethoxypyrimidine as the major hydrolyzed
product. In soils, O-demethylated amidosulfuron is the
major degradation product. In mammals and plants,
primary hydroxylation at the pyrimidine ring is a
characteristic degradation reaction yielding
5-hydroxyamidosulfuron. |
| | Amidosulfuron Preparation Products And Raw materials |
|
