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TOLFENPYRAD

TOLFENPYRAD Suppliers list
Company Name: Hebei Dueling International Trade Co. LTD  Gold
Tel: 18032116176
Email: 399549586@qq.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Chembest Research Laboratories Limited  
Tel: 021-20908456
Email: sales@BioChemBest.com
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
Email: sales@chemreagents.com

TOLFENPYRAD manufacturers

  • Tolfenpyrad
  • Tolfenpyrad pictures
  • $35.00
  • 2026-07-14
  • CAS:129558-76-5
  • Purity: 97.00%
  • Supply Ability: 10g
  • Tolfenpyrad
  • Tolfenpyrad pictures
  • 2024-12-24
  • CAS:129558-76-5
  • Min. Order: 1Kg
  • Purity: 99.99%
  • Supply Ability: 20 tons
  • TOLFENPYRAD
  • TOLFENPYRAD pictures
  • $10.00
  • 2023-08-04
  • CAS:129558-76-5
  • Min. Order: 1kg
  • Purity: 99.99%
  • Supply Ability: 50000tons
TOLFENPYRAD Basic information
Description References
Product Name:TOLFENPYRAD
Synonyms:omi-88;tolfenpyrad (bsi, pa iso);TOLFENPYRAD STANDARD;HATI-HATI;1H-Pyrazole-5-carboxaMide, 4-chloro-3-ethyl-1-Methyl-N-[[4-(4-Methylphenoxy)phenyl]Methyl]-;TOLFENPYRAD;mmbc mab-c mmb-chminaca fubamb;4-Chloro-3-ethyl-1-methyl-N-[4-(p-tolyloxy)benzyl]pyrazole-5-carboxamide
CAS:129558-76-5
MF:C21H22ClN3O2
MW:383.87
EINECS:
Product Categories:Pharmaceutical intermediates;Heterocycles;Aromatics;Amines;Agro-Products
Mol File:129558-76-5.mol
TOLFENPYRAD Structure
TOLFENPYRAD Chemical Properties
Melting point 87~89℃
Boiling point 540.0±50.0 °C(Predicted)
density 1.21±0.1 g/cm3(Predicted)
storage temp. 0-6°C
solubility Chloroform (Slightly), DMSO (Slightly)
form Solid
pka13.11±0.46(Predicted)
color White to off-white
BRN 13666608
InChIInChI=1S/C21H22ClN3O2/c1-4-18-19(22)20(25(3)24-18)21(26)23-13-15-7-11-17(12-8-15)27-16-9-5-14(2)6-10-16/h5-12H,4,13H2,1-3H3,(H,23,26)
InChIKeyWPALTCMYPARVNV-UHFFFAOYSA-N
SMILESN1(C)C(C(NCC2=CC=C(OC3=CC=C(C)C=C3)C=C2)=O)=C(Cl)C(CC)=N1
CAS DataBase Reference129558-76-5
EPA Substance Registry System1H-Pyrazole-5-carboxamide, 4-chloro-3-ethyl-1-methyl-N-[[4-(4-ethylphenoxy)phenyl]methyl]- (129558-76-5)
Safety Information
Hazard Codes Xn,N
Risk Statements 20/22-50/53
Safety Statements 60-61
RIDADR UN 3077 9 / PGIII
WGK Germany 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Inhalation
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
MSDS Information
TOLFENPYRAD Usage And Synthesis
DescriptionTolfenpyrad is a pyrazole insecticide developed by Mitsubishi Chemical. It was first approved in 2002 in Japan under the trade name of Hachi-hachi.
It has broad insecticidal activity against a variety of pests such as Hemiptera, Coleoptera, Diptera, Lepidoptera, Thysanoptera and Acarina. It is especially effective against pests that are resistant to existing insecticides such as organophosphates and carbametes, because it supposedly possesses a new mode of action: inhibition of Complex I in the respiratory electron-transfer chain of mitochondria. It is applied for vegetables particularly cruciferous leafy varieties, cucurbits, cole crops, tea, fruits & nuts, selected row crops, and indoor ornamentals except cut flowers.
References[1] http://sitem.herts.ac.uk/aeru/iupac/Reports/1687.htm  
[2] Koji Yamaguchi,  Wakako Hikiji, Masahiko Takino, Kanju Saka, Makiko Hayashida, Tatsushige Fukunaga, Youkichi Ohno (2012) Analysis of Tolfenpyrad and its Metabolites in Plasma in a Tolfenpyrad Poisoning Case, 36, 529-537
UsesTolfenpyrad
DefinitionChEBI: An aromatic amide obtained by formal condensation of the carboxy group of 4-chloro-3-ethyl-1-methylpyrazole-5-carboxylic acid with the amino group of 1-[4-(4-methylphenoxy)phenyl]methylamine.
Production MethodsTolfenpyrad is commercially produced via a process that involves the condensation of 4-chloro-3-ethyl-1-methylpyrazole-5-carboxylic acid with 1-[4-(4-methylphenoxy)phenyl]methylamine, forming a carboxamide linkage. This multi-step synthesis requires precise control of reaction conditions to ensure high purity and yield.
Mechanism of actionBroad-spectrum, contact activity, exhibits antifeedant activity especially against Lepidoptera. Mitochondrial complex I electron transport inhibitor.
Pesticide TypeInsecticide; Fungicide
TOLFENPYRAD Preparation Products And Raw materials
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