Nicosulfuron 4% Od

Nicosulfuron 4% OD

Nicosulfuron NOMENCLATURE
Common name nicosulfuron (BSI, ANSI, E-ISO, (m) F-ISO); no name (Brazil) 
IUPAC name 2-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-N,N-dimethylnicotinamide; 1-(4,6-dimethoxypyrimidin-2-yl)-3-(3-dimethylcarbamoyl-2-pyridylsulfonyl)urea
Chemical Abstracts name 2-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-N,N-dimethyl-3-pyridinecarboxamide 
CAS RN [111991-09-4] 

Nicosulfuron APPLICATIONS
Nicosulfuron Biochemistry Branched chain amino acid synthesis (ALS or AHAS) inhibitor. Acts by inhibiting biosynthesis of the essential amino acids valine and isoleucine, hence stopping cell division and plant growth. Maize selectivity derives from selective metabolism (P450-mediated pyrimidine-5-hydroxylation, followed by conjugation with glucose).

Nicosulfuron Mode of action Selective systemic herbicide, absorbed by the foliage and roots, with rapid translocation in xylem and phloem to the meristematic tissues.

Nicosulfuron Uses Selective post-emergence control in maize of annual grass weeds, including Setaria, Echinochloa, Digitaria, Panicum, Lolium and Avena spp., broad-leaved weeds, including Amaranthus spp. and Cruciferae, and perennials such as Sorghum halepense and Agropyron repens. Applied at 35-70 g/ha.


Nicosulfuron 4% OD

Nicosulfuron NOMENCLATURE
Common name nicosulfuron (BSI, ANSI, E-ISO, (m) F-ISO); no name (Brazil) 
IUPAC name 2-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulfamoyl)-N,N-dimethylnicotinamide; 1-(4,6-dimethoxypyrimidin-2-yl)-3-(3-dimethylcarbamoyl-2-pyridylsulfonyl)urea
Chemical Abstracts name 2-[[[[(4,6-dimethoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-N,N-dimethyl-3-pyridinecarboxamide 
CAS RN [111991-09-4] 

Nicosulfuron APPLICATIONS
Nicosulfuron Biochemistry Branched chain amino acid synthesis (ALS or AHAS) inhibitor. Acts by inhibiting biosynthesis of the essential amino acids valine and isoleucine, hence stopping cell division and plant growth. Maize selectivity derives from selective metabolism (P450-mediated pyrimidine-5-hydroxylation, followed by conjugation with glucose).

Nicosulfuron Mode of action Selective systemic herbicide, absorbed by the foliage and roots, with rapid translocation in xylem and phloem to the meristematic tissues.

Nicosulfuron Uses Selective post-emergence control in maize of annual grass weeds, including Setaria, Echinochloa, Digitaria, Panicum, Lolium and Avena spp., broad-leaved weeds, including Amaranthus spp. and Cruciferae, and perennials such as Sorghum halepense and Agropyron repens. Applied at 35-70 g/ha.

Hoisting Tackle

This aluminum alloy and MC nylon sheave hoisting tackle possesses light dead weight, which is equipped with the aluminum alloy side panel and the MC nylon sheave. This single Sheave Pulley block is the open type. Our product can be used for lifting heavy objects and other operations in the line construction.

Our iron hoisting block is widely applicable to the erection of overhead line structures, lifting equipment, and other hoisting operations. This product is classified as hook style (G), ring style (H), or clevis style (B). Thus, the style our customer needs must be clearly indicated in the contract when the order is placed.

Hoisting Tackle,Nylon Sheave Hoisting Tackle, Single Wheel Block, Dual Sheave Hoisting Tackle, Open Type Pulley Block,Stringing Conductor Pulley Block

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