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Saflufenacil

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Company Name: Hebei Zhuanglai Chemical Trading Co Ltd
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Products Intro: Product Name:Saflufenacil
CAS:372137-35-4
Purity:99 Package:1kg;50USD
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:Saflufenacil
CAS:372137-35-4
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Company Name: Alfa Chemistry
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Products Intro: Product Name:Saflufenacil
CAS:372137-35-4
Purity:96%
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Products Intro: Product Name:2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-...
CAS:372137-35-4
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
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Products Intro: Product Name:Saflufenacil
CAS:372137-35-4
Purity:NLT 98% Remarks:MC551721

Saflufenacil manufacturers

  • Saflufenacil
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  • $50.00
  • 2025-05-23
  • CAS:372137-35-4
  • Min. Order: 1kg
  • Purity: 99
  • Supply Ability: 5000

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Saflufenacil Basic information
Product Name:Saflufenacil
Synonyms:Saflufenacil;Saflufenacil@100 μg/mL in Methanol;Saflufenacil@1000 μg/mL in Acetonitrile;Benzamide, 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]sulfonyl]-;2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-...;Kixor;Kixor Herbicide;Benodanil Impurity 5
CAS:372137-35-4
MF:C17H17ClF4N4O5S
MW:500.85
EINECS:
Product Categories:372137-35-4
Mol File:372137-35-4.mol
Saflufenacil Structure
Saflufenacil Chemical Properties
density 1.542±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO ()Slightly, Methanol (Slightly)
pka4.24±0.40(Predicted)
BRN 11326826
Major Applicationagriculture
environmental
InChIInChI=1S/C17H17ClF4N4O5S/c1-8(2)25(4)32(30,31)23-15(28)9-5-12(11(19)6-10(9)18)26-14(27)7-13(17(20,21)22)24(3)16(26)29/h5-8H,1-4H3,(H,23,28)
InChIKeyGNHDVXLWBQYPJE-UHFFFAOYSA-N
SMILESC(NS(N(C)C(C)C)(=O)=O)(=O)C1=CC(N2C(=O)N(C)C(C(F)(F)F)=CC2=O)=C(F)C=C1Cl
EPA Substance Registry SystemBenzamide, 2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-4-fluoro-N-[[methyl(1-methylethyl)amino]sulfonyl]- (372137-35-4)
Safety Information
Hazard Codes N
Risk Statements 50/53
Safety Statements 61
RIDADR UN 3077 9 / PGIII
WGK Germany 2
Storage Class11 - Combustible Solids
Hazard ClassificationsAquatic Acute 1
Aquatic Chronic 1
MSDS Information
Saflufenacil Usage And Synthesis
UsesSaflufenacil-d7 is the labeled version of Saflufenacil (S081800), which is a herbicide of the pyrimidinedione chemical class used for the preplant burndown and selective preemergence dicot weed control in different field crops. It was found to inhibit protoporphyrinogen IX oxidase (PPO) enzyme.
DefinitionChEBI: Saflufenacil is a member of the class of sulfamides that is sulfamide in which one of the amino groups has been substituted by a methyl group an an isopropyl group, while the other has been substituted by a 2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzoyl group. An important BASF herbicide, not registered in Europe but sold in USA, Canada and several other countries to control weeds in a wide range of food crops. Often mixed with other products such as glyphosate. It has a role as an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor, a herbicide and an agrochemical. It is a member of monochlorobenzenes, a member of monofluorobenzenes and a member of sulfamides. It is functionally related to a uracil.
SynthesisA preparation method of saflufenacil is characterized by comprising the following steps:
(1) adding an I-methyl intermediate and a solvent into an organic solvent, and carrying out continuous chlorination reaction under pressure to obtain an intermediate I-trichlorobenzyl;
(2) adding I-trichlorobenzyl and a sulfuryl diamide intermediate into an organic solvent for condensation reaction to obtain a product saflufenacil;
the reaction formula is as follows:
Synthesis of Saflufenacil
Mode of actionPhysiological and biochemical profiling confirmed that saflufenacil was a protoporphyrinogen-IX-oxidase (PPO) inhibitor. Saflufenacil elicits symptoms similar to other peroxidizing herbicides, including rapid, light-dependent necrosis of foliar tissue. Saflufenacil is readily absorbed by the root and shoot tissue of plants. Once absorbed, Saflufenacil is predominantly translocated via the xylem, with limited movement via the phloem. Saflufenacil is highly effective in controlling dicot weeds through contact and residual activity. In addition to non-crop and pre-plant burndown utility, saflufenacil demonstrates preemergence selectivity in a wide range of crops. Selectivity is conferred by physical placement and rapid metabolism of saflufenacil in tolerant crop species such as corn.
Pesticide TypeHerbicide
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