Identification | More | [Name]
Amidosulfuron | [CAS]
120923-37-7 | [Synonyms]
AMIDOSULFURON GRATIL n-(((((4,6-dimethoxy-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)-n-methylmethanesulfonamide Amidosulfuron PESTANAL METHYLMETHANESULFONAMIDE 1-(4,6-Dimethoxypyrimidin-2-yl)-3-(N-mesyl-N-methylsulfamoyl)urea | [EINECS(EC#)]
407-380-0 | [Molecular Formula]
C9H15N5O7S2 | [MDL Number]
MFCD01310639 | [Molecular Weight]
369.37 | [MOL File]
120923-37-7.mol |
Questions And Answer | Back Directory | [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. |
Chemical Properties | Back Directory | [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) | [form ]
neat | [pka]
0.12±0.40(Predicted) | [color ]
White to Off-White | [Stability:]
Hygroscopic, Unstable in Solution | [LogP]
1.630 | [CAS DataBase Reference]
120923-37-7(CAS DataBase Reference) |
Safety Data | Back Directory | [Risk Statements ]
R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [WGK Germany ]
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Hazard Information | Back Directory | [Uses]
Herbicide. | [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. |
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