Keywords

• BUPIRIMATE
• C13H24N4O3S
• 41483-43-6

Quick Details

• ProName: Manufacturer of BUPIRIMATE at Factory ...
• CasNo: 41483-43-6
• Molecular Formula: C13H24N4O3S
• Appearance: Light brown ceraceous solid.
• Application: Agrochemical technical
• DeliveryTime: 3-5days after payment comfirmed
• PackAge: 25kg/fiber drum
• Port: Any port in China
• ProductionCapacity: 6000 Metric Ton/Year
• Purity: 99%
• Storage: Stored in cool and dried place
• Transportation: by sea or by air
• LimitNum: 25 Kilogram
• Related Substances: Water
• Residue on Ignition: 0.03%Max
• Heavy Metal: NMT 10ppm
• Valid Period: 2 years
• Heavy metals: <10ppm

Superiority

We are one of the domestic largest manufacturers of API;

We are always supplier of products with higher quality and at more competitive price;

We are supplier of safe and ecofriendly products ;

We provide stable supply and efficient service;

Delivery in time;

Cooperate with scientific research institutions to keep the leading position on the field of technology.

We can provide products to all customers all over the world.


 

Details

BUPIRIMATE Basic information

Product Name:    BUPIRIMATE
Synonyms:    NIMROD;2-aethylamino-5-butyl-4-yl-dimethylsulfamat;-4-ol;dimethyl-sulfamicaci5-butyl-2-(ethylamino)-6-methyl-4-pyrimidinylester;dimethylsulfamicacid5-butyl-2-(ethylamino)-6-methyl-4-pyrimidinylester;n,n-dimethyl-sulfamicaciesterwith5-butyl-2-ethylamino-6-methylpyrimidin;nimrodt;pp588
CAS:    41483-43-6
MF:    C13H24N4O3S
MW:    316.42
EINECS:    255-391-2
Product Categories:    BI - BZBuilding Blocks;PyrimidinesPesticides;A-BAlphabetic;Alpha sort;B;Fungicides;Heterocyclic Building Blocks;Pesticides&Metabolites;Pyrimidines
Mol File:    41483-43-6.mol

BUPIRIMATE Chemical Properties

Fp     100 °C
storage temp.     0-6°C
Merck     13,1482
EPA Substance Registry System    Sulfamic acid, dimethyl-, 5-butyl-2-(ethylamino)-6-methyl- 4-pyrimidinyl ester(41483-43-6)

Usage    Bupirimate is a pyrimidine based fungicide with protective and curative activity for the control of fungal diseases by interfearing with nucleic acid synthesis.