Basic information Description References Safety Supplier Related
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Diflufenican

Basic information Description References Safety Supplier Related

Diflufenican Basic information

Product Name:
Diflufenican
Synonyms:
  • PELICAN(TM)
  • n-(2,4-difluorophenyl)-2-(3-(trifluoromethyl)phenoxy)-3-pyridinecarboxamide
  • 2,4-DIFLUORO-2-(A, A, A-TRIFLUORO-M-TOLYLOXY)-NICOTINANILIDE
  • FENICAN
  • JAVELIN
  • Couger
  • DIFLUFENICAN PESTANAL, 100 MG
  • DIFLUFENICAN:2,4-DIFLUORO-2-( A , A , A -TRIFLUORO-M-TOLYLOXY)-NICOTINANILIDE
CAS:
83164-33-4
MF:
C19H11F5N2O2
MW:
394.29
Product Categories:
  • Agro-Products
  • Amines
  • aldehydes
  • Intermediates & Fine Chemicals
  • Aromatics
  • Heterocycles
  • Mutagenesis Research Chemicals
  • Pharmaceuticals
  • Alpha sort
  • AmidePesticides&Metabolites
  • D
  • DAlphabetic
  • DID - DIN
  • Herbicides
  • Detergents
  • Pesticides&Metabolites
Mol File:
83164-33-4.mol
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Diflufenican Chemical Properties

Melting point:
110°C
Boiling point:
376.2±42.0 °C(Predicted)
Density 
1.4301 (estimate)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Acetone (Slightly), Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly),
pka
9.03±0.70(Predicted)
color 
Off-White
Merck 
14,3144
BRN 
4212494
InChIKey
WYEHFWKAOXOVJD-UHFFFAOYSA-N
LogP
4.900
CAS DataBase Reference
83164-33-4(CAS DataBase Reference)
EPA Substance Registry System
3-Pyridinecarboxamide, N-(2,4-difluorophenyl)-2-[3-(trifluoromethyl)phenoxy]- (83164-33-4)
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Safety Information

Risk Statements 
52/53
Safety Statements 
61
RIDADR 
UN3077(solid); UN3082 (liquid)
WGK Germany 
2
RTECS 
US4589800
HS Code 
2933.39.2500
Toxicity
LD50 in mice, rats (mg/kg): >1000, >2000 orally; in rats (mg/kg): >2000 dermally (Cramp)

MSDS

  • Language:English Provider:Kwarc
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Diflufenican Usage And Synthesis

Description

The diflufenican is a selective contact and residual herbicide that can be applied pre-emergence and post-emergence. It can be absorbed through the shoots of the germinating seeding with limited translocation. Its mode of mechanism is via a bleaching action through inhibiting the carotenoid biosynthesis process, further blocking photosynthesis process and causing plant death. It is used for the treatment of some broad leaved weeds such as Stellaria media (Chickweed), Veronica Spp (Speedwell), Viola spp, Geranium spp (Cranesbill) and Laminum spp (Dead nettles). It has been approved for use on barley, durum wheat, rye, triticale and wheat. It can be used in combination with isoproturon or other cereal herbicides.

References

http://www.globachem.com/en/agrochemicals/d/resource/diflufenican
http://www.agchemaccess.com/Diflufenican

Uses

Pre and post emergence foliar absorbed herbicide for winter weed control in cereal crops; carotenoid biosynthesis inhibitor.

Uses

Herbicide.

Definition

ChEBI: A pyridinecarboxamide that is pyridine-3-carboxamide substituted by a 2,4-difluorophenyl group at the carbamoyl nitrogen and a 3-(trifluoromethyl)phenoxy group at position 2.

Agricultural Uses

Herbicide: Pre-and post-emergence foliar absorbed herbicide for winter weed control in cereal crops; carotenoid biosynthesis inhibitor. Used on crops such as apples, apricot, barley, beans (dry), broad beans, cherry, grapefruit, lemon, lime, loquat, natsudaidai (whole), nectarine, orange, peach, pear, peas, persimon, plum,quince, rye, soybeans, unshu orange and wheat. Not currently registered in the U.S. Approved for use in EU countries.

Trade name

ARDENT®; BACARA®; CAPTURE® Diflufenican; COUGAR®; CUB®; GRENADIER®; IONIZ®; JAVELIN®; JAVELIN® GOLD; KWARC®; MB-38183®; M&B 38544®; PANTHER®; QUARTZ®; SPEARHEAD®

Diflufenican Preparation Products And Raw materials

Raw materials

DiflufenicanSupplier

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