2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se

Model NO.: SE
Formulation Types: Se
CAS: 145701-23-1
Trademark: Essence
Transport Package: 10ml ~200L for Liquid Formulations,
Specification: FAO, WHO
Origin: China
HS Code: 3808
Model NO.: SE
Formulation Types: Se
CAS: 145701-23-1
Trademark: Essence
Transport Package: 10ml ~200L for Liquid Formulations,
Specification: FAO, WHO
Origin: China
HS Code: 3808
2,4-D-ethylhexyl 452.4g/L + Florasulam 0.6g/L SE
 

Mode of action

Selective systemic herbicide. Salts are readily absorbed by the roots, whilst esters are readily absorbed by the foliage. Translocation occurs, with accumulation principally at the meristematic regions of shoots and roots. Acts as a growth inhibitor.

Targets

Grass

Crops

Cereals, maize, sorghum, grassland

Main customer benefits

Longer Lasting Control

Consistent Performance

Secures Yield

New Mode of Action  

Florasulam NOMENCLATURE
Common name florasulame ((m) F-ISO); florasulam (BSI, E-ISO) 
IUPAC name 2′,6′,8-trifluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonanilide
Chemical Abstracts name N-(2,6-difluorophenyl)-8-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide 
CAS RN [145701-23-1] 

Florasulam APPLICATIONS
Florasulam Biochemistry Branched chain amino acid (leucine, isoleucine and valine) synthesis (ALS or AHAS) inhibitor. Selectivity in wheat is due to differential metabolism.

Florasulam Mode of action Taken up by roots and shoots, and translocated in both xylem and phloem.

Florasulam Uses Herbicide for post-emergence control of broad-leaved weeds, especially Galium aparine, Stellaria media, Polygonum convolvulus, Matricaria spp. and various cruciferae, in cereals and maize, at rates up to 7.5 g/ha.

2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se 2,4-D-ethylhexyl 452.4g/L + Florasulam 0.6g/L SE
 

Mode of action

Selective systemic herbicide. Salts are readily absorbed by the roots, whilst esters are readily absorbed by the foliage. Translocation occurs, with accumulation principally at the meristematic regions of shoots and roots. Acts as a growth inhibitor.

Targets

Grass

Crops

Cereals, maize, sorghum, grassland

Main customer benefits

Longer Lasting Control

Consistent Performance

Secures Yield

New Mode of Action  

Florasulam NOMENCLATURE
Common name florasulame ((m) F-ISO); florasulam (BSI, E-ISO) 
IUPAC name 2′,6′,8-trifluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonanilide
Chemical Abstracts name N-(2,6-difluorophenyl)-8-fluoro-5-methoxy[1,2,4]triazolo[1,5-c]pyrimidine-2-sulfonamide 
CAS RN [145701-23-1] 

Florasulam APPLICATIONS
Florasulam Biochemistry Branched chain amino acid (leucine, isoleucine and valine) synthesis (ALS or AHAS) inhibitor. Selectivity in wheat is due to differential metabolism.

Florasulam Mode of action Taken up by roots and shoots, and translocated in both xylem and phloem.

Florasulam Uses Herbicide for post-emergence control of broad-leaved weeds, especially Galium aparine, Stellaria media, Polygonum convolvulus, Matricaria spp. and various cruciferae, in cereals and maize, at rates up to 7.5 g/ha.

2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se
2, 4-D-Ethylhexyl 452.4g/L + Florasulam 0.6g/L Se

Double colored plastic handle

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