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mesotrione, mesotrione herbicide , agricultural product

mesotrione, mesotrione herbicide , agricultural product

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Contact Person Mr. Carlson

405 GLAD STONE HEIGHTS CNR PRETORIUS AND EDITH CARVEL STREET, JOHANNESBURG, GAUTENG

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Description

Quick Details
Classification:
Herbicide
CAS No.:
**********8
Other Names:
Mesotrione
MF:
C*4H*3NO7S
Place of Origin:
South Africa
State:
Powder
Purity:
*4%TC 9%SC
Application:
Herbicide
Brand Name:
Shurong
Model Number:
TC and SC
color:
Pale yellow
Especially for:
Corn
Security:
Very good
Stock:
sufficient stodk
Toxicity:
low toxicity
Formulation:
*4%TC 9%SC
Packaging & Delivery
Packaging Details: solid: *5kg/bag, *0kg/bag liquid: 1l/bottle, *5kg/drum or to customers\' request.
Delivery Detail: *5 days after order confirmed

Common name:

 Mesotrione

Chemical Name: [*-[*-(methylsulfonyl)**-nitrobenzoyl]*1, *-cyclohexanedione
Physical & Chemical Character:

Appearance: Light yellow crystal powder or light brown liquid

Melting Point: **5°C

Density :1.*6g/ ml (*0°C) 

Boiling Point:4.*7×***8mmHg (*0°C). 

Applications: Mesotrione will be applied pre- and post-emergence through ground or aerial application equipment. Mesotrione has herbicidal activity against broadleaf weeds. It\'s efficacy is the result of the inhibition of the enzyme *-hydroxyphenylpyruvate dioxygenase (HPPD) enzyme in target plants. Following treatment, in sensitive plants carotenoid biosynthesis is disrupted in the chlorophyll pathway, resulting in a bleaching effect.
Mode of action:

p-Hydroxyphenyl pyruvate dioxygenase inhibitor, which ultimately affects carotenoid biosynthesis. Selectivity in maize derives from differential metabolism (to the *-hydroxy derivative) and also possibly from slower foliar uptake. Uptake is foliar and via the root, with both acropetal and basipetal translocation. Symptoms are whitening of leaves, followed by necrosis of the meristematic tissue.

Use:
Under development for pre- (at ******5 g/ha) and post- (at *****0 g/ha) emergence control of broad-leaved weeds, such as Xanthium strumarium, Ambrosia trifida, Abutilon theophrasti, and Chenopodium, Amaranthus and Polygonum spp., and some grass weeds, in maize.
Biochemistry: p-Hydroxyphenyl pyruvate dioxygenase inhibitor, which ultimately affects carotenoid biosynthesis. Selectivity in maize derives from differential metabolism.

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