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Chlorantraniliprole

CAS No.
500008-45-7
Chemical Name:
Chlorantraniliprole
Synonyms
CHLOANTRANILIPROLE;Clorantraniliprole;Chlorantranilipol;Chlorantraniliprole [iso];Chlorantraniliprole 35%WDG;3-Bromo-4-chloro-1-(3-chloro-2-pyridyl)-2-methyl-6-(methylcarbamoyl)pyrazole-5-carboxanilide;3-Bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide;Coragen;Altacor;Rynaxpyr
CBNumber:
CB01404014
Molecular Formula:
C18H14BrCl2N5O2
Molecular Weight:
483.15
MDL Number:
MFCD11840831
MOL File:
500008-45-7.mol
Last updated:2025-11-10 14:44:25
Product description Number Pack Size Price
Chlorantraniliprole PESTANAL®, analytical standard 32510 25 mg $130
Chlorantraniliprole 24140 10mg $57
Chlorantraniliprole 24140 25mg $109
Chlorantraniliprole 24140 5mg $32
Chlorantraniliprole 24140 50mg $184

Chlorantraniliprole Properties

Melting point approximate 225℃ (dec.)
Boiling point 526.6±50.0 °C(Predicted)
Density 1.66±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Chloroform: Slightly Soluble; DMSO: Slightly Soluble
form A solid
pka 10.19±0.70(Predicted)
color White to off-white
InChI InChI=1S/C18H14BrCl2N5O2/c1-9-6-10(20)7-11(17(27)22-2)15(9)24-18(28)13-8-14(19)25-26(13)16-12(21)4-3-5-23-16/h3-8H,1-2H3,(H,22,27)(H,24,28)
InChIKey PSOVNZZNOMJUBI-UHFFFAOYSA-N
SMILES N1(C2=NC=CC=C2Cl)C(C(NC2=C(C(NC)=O)C=C(Cl)C=C2C)=O)=CC(Br)=N1
LogP 3.641 (est)
CAS DataBase Reference 500008-45-7
FDA UNII 622AK9DH9G
EPA Substance Registry System 1H-Pyrazole-5-carboxamide, 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)- (500008-45-7)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P391-P501
Hazard Codes  Xn
Risk Statements  22-36/37
Safety Statements  26
Hazardous Substances Data 500008-45-7(Hazardous Substances Data)
NFPA 704
0
2 0

Chlorantraniliprole price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 32510 Chlorantraniliprole PESTANAL®, analytical standard 500008-45-7 25 mg $130 2025-07-31 Buy
Cayman Chemical 24140 Chlorantraniliprole 500008-45-7 10mg $57 2024-03-01 Buy
Cayman Chemical 24140 Chlorantraniliprole 500008-45-7 25mg $109 2024-03-01 Buy
Cayman Chemical 24140 Chlorantraniliprole 500008-45-7 5mg $32 2024-03-01 Buy
Cayman Chemical 24140 Chlorantraniliprole 500008-45-7 50mg $184 2024-03-01 Buy
Product number Packaging Price Buy
32510 25 mg $130 Buy
24140 10mg $57 Buy
24140 25mg $109 Buy
24140 5mg $32 Buy
24140 50mg $184 Buy

Chlorantraniliprole Chemical Properties,Uses,Production

Description

Chlorantraniliprole (Rynaxpyr) is an insecticide of the ryanoid class. It is a new compound by DuPont belonging to a new class of selective insecticides (anthranilic diamides) featuring a novel mode of action (group 28 in the IRAC classification). It is the first anthranilic diamide registered for use on turfgrass and landscape ornamentals. It is used to control a broad spectrum of pests including cabbage loopers, corn borers, Colorado potato beetle, European grapevine moth, armyworms and cutwormson a range of crops including potatoes and cotton. Its mechanism of action is through activating the insect ryanodine receptors (RyRs), further stimulating the release and depletion of intracellular calcium stores from the sarcoplasmic reticulum of muscle cells, causing impaired muscle regulation, paralysis and ultimately death of sensitive species.

Description

Chlorantraniliprole is an anthranilic diamide insecticide and agonist of ryanodine receptors located on the sarcoplasmic reticulum in muscle and endoplasmic reticulum in non-muscle cells. It binds to a different site than ryanodine on the receptor and stimulates the release of calcium from intracellular stores with EC50 values ranging from 40 to 50 nM for P. americana neurons and H. virescens or D. melanogaster recombinant ryanodine receptors. It is highly selective for insect over mammalian ryanodine receptors (EC50s = 14,000 nM, >100 μM, and >100 μM for C2C12 mouse, PC12 rat, and IMR32 human cells, respectively). Chlorantraniliprole is active against insects of the order Lepidoptera, including larvae of the fall armyworm (S. frugiperda), diamondback moth (P. xylostella), and tobacco budworm (H. virescens) with EC50 values of 0.02, 0.01, and 0.05 ppm, respectively, and of the orders Coleoptera, Diptera, and Isoptera. Formulations containing chlorantraniliprole have been used in agriculture to control moths, beetles, and caterpillars among other insects.

Chemical Properties

White crystal, specific gravity (for liquid) 1.507g/mL, melting point 208-210℃, decomposition temperature 330℃, vapor pressure (under 20~25) 6.3×1012Pa, solubility (under 20~25, mg/L): water 1.023, acetone 3.446, methanol 1.714, acetonitrile 0.711, ethyl acetate 1.144. Chlorfenvinphos It is highly efficient and broad-spectrum, and has good control effect on Lepidoptera of Noctuidae, stem borer moths, fruit moths, leaf roller moths, pink moths, vegetable moths, wheat moths, and fine moths, etc. It can also control Sphingidae weevils, leaf beetles; Diptera subterranean flies; sooty fly and many other non-lepidopteran pests.

Uses

Chlorantraniliprole is a pyrazolylpyridine insecticide and an activator of insect ryanodine receptor. Used in Pesticide detection. (Solution)

Definition

ChEBI: Chlorantraniliprole is a carboxamide resulting from the formal condensation of the carboxylic acid group of 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid with the primary amino group of 2-amino-5-chloro-N,3-dimethylbenzamide. The first of the anthranilic diamide insecticides, it is a ryanodine receptor activator and is used to protect a wide variety of crops, including corn, cotton, grapes, rice and potatoes. It has a role as a ryanodine receptor agonist. It is an organobromine compound, a member of pyridines, a member of pyrazoles, a pyrazole insecticide, a member of monochlorobenzenes and a secondary carboxamide.

Preparation

Chlorantraniliprole was synthesized by reaction of 3-bromo-1-(3-chloropyridin-2-pyridinyl)-1H-pyrazole-5carboxylic acid with 2-amino-5-chloro-3-methylbenzoic acid.3-bromo-1-(3-chloropyridin-2-pyridinyl)-1H-pyrazole5-carboxylic acid was prepared by reaction of maleic anhydride with 2,3-dichloropyridine as starting materials in eight steps.2-Amino-5-chloro-3-methylbenzoic acid was prepared by reaction of 2-amino-3-methylbenzoic acid in one step.The structure of target compound was conf irmed by 1H NMR.Total yield was 36.3%(calculated with 2,3-dichloropyridine),and purity determined by HPLC was over 95%.

Synthesis

3-BroMo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid

500011-86-9

2H-3,1-Benzoxazine-2,4(1H)-dione, 6-chloro-8-methyl-

120374-68-7

Methylamine

74-89-5

Chlorantraniliprole

500008-45-7

A mixture of 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid (93.6% purity, 16.16 g, 50.0 mmol), 6-chloro-8-methyl-2,4-dihydro-1H-3,1-benzoxazine-2,4-dione (99.0% purity, 11.22 g, 52.5 mmol), and 3-methylpyridine (16.5 mL. 15.8 g, 170 mmol) were added slowly and dropwise to an acetonitrile (15 mL) solution of methanesulfonyl chloride (5.0 mL, 7.4 g, 65 mmol) in acetonitrile (65 mL) at -5 °C. The reaction mixture was stirred at -5 to 0 °C for 15 minutes before being warmed to 50 °C and maintained for 4 hours. Subsequently, the reaction system was cooled to room temperature, water (29 mL) was added slowly and dropwise, and stirring was continued for 15 minutes. Next, 40% aqueous methylamine solution (20.0 mL, 17.9 g, 231 mmol) was added all at once and stirred overnight at room temperature. After completion of the reaction, the mixture was filtered, and the solid was washed sequentially with 2:1 acetonitrile-water (2 × 30 mL) and pure acetonitrile (3 × 30 mL), and dried under nitrogen protection to afford the target product, 3-bromo-N-(4-chloro-2-methyl-6-(methylcarbamoyl)phenyl)-1-(3-chloro-pyridin-2-yl)-1H-pyrazole-5-carboxamide, as a light yellow powder, 22.44 g (HPLC purity 95.5%, yield calculated based on purity 88.7%). The structure of the product was confirmed by 1H NMR (CDCl3): δ 2.18 (s, 3H), 2.95 (s, 3H), 6.21 (m, 1H), 7.10 (s, 1H), 7.24 (m, 2H), 7.39 (m, 1H), 7.80 (d, 1H), 8.45 (d, 1H).

References

[1] Patent: WO2004/111030, 2004, A1. Location in patent: Page 42

500011-86-9
890707-28-5
500008-45-7
Synthesis of Chlorantraniliprole from 3-BroMo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid and Bardoxolone

Chlorantraniliprole Suppliers

Global( 80)Suppliers
Supplier Tel Email Country ProdList Advantage
Qingdao Trust Agri Chemical Co.,Ltd
+86-008615963231493 +86-008613573296305 trustagri@hotmail.com China 301 58
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32435 58
Shandong Hanjiang Chemical Co., Ltd
+86-0533-2066820 +8618369939125 hanson@sdhanjiang.com China 999 58
Compound Net Biotechnology Inc.
+8615303909093 sales@compound-net.com China 2914 58
Shaanxi Dideu New Materials Co. Ltd
+86-18192503167 18192503167; 1036@dideu.com China 7531 58
Changsha Hongyuxiang Chemical Co., Ltd
+8613757949618 info@hoyoshee.com China 105 58
Alchemie Shanghai Co.,Ltd.
+8615921545397 cindy_hu@alchemie-shanghai.com China 133 58
Wuhan lanabai Pharmaceutical Chemical Co., Ltd 15307151931 2355680@qq.com China 5831 58
Shanghai Macklin Biochemical Co.,Ltd. 021-50706066 15221275939 shenlinxing@macklin.cn China 14580 58

View Lastest Price from Chlorantraniliprole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
chlorantraniliprole pictures 2025-12-02 chlorantraniliprole
500008-45-7
US $0.00 / kg 1kg 99 20tons Qingdao Trust Agri Chemical Co.,Ltd
Chlorantraniliprole pictures 2025-12-01 Chlorantraniliprole
500008-45-7
US $0.00 / kg 1kg 98% 1000kg Shaanxi Dideu New Materials Co. Ltd
Chlorantraniliprole pictures 2025-11-09 Chlorantraniliprole
500008-45-7
US $39.00-105.00 / mg 98.86% 10g TargetMol Chemicals Inc.

Chlorantraniliprole Spectrum

CHLORANTRANILIPROLE Rynaxpyr DPX E2Y45 Chlorantraniliprole 95% Chlorantraniliprole Standard Coragen Chlorantraniliprole 95% (Rynaxypyr, Coragen) Chlorantraniliprole Solution, 1000ppm 1H-Pyrazole-5-carboxamide,3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)- 5-bromo-N-[2-chloro-4-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridinyl)-3-pyrazolecarboxamide 5-bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloropyridin-2-yl)pyrazole-3-carboxamide Chlorantraniliprole@100 μg/mL in Methanol Chlorantraniliprole@1000 μg/mL in Methanol [Carbonyl-14C1]14C-chlorantraniliprole Chlorantraniliprole Solution Chlorantraniliprole Solution in Methanol, 100μg/mL Altacor Clorantraniliprole 35% WDG Chlorantraniliprole Solution (0.1 mg/mL in 1:1 Acetonitrile/MeOH) Chlorantraniliprole 95%TC & 35%WG Chlorantraniliprole 95%TC Altacor (Chlorantraniliprole 35% WG) CHLOANTRANILIPROLE 3-Bromo-4-chloro-1-(3-chloro-2-pyridyl)-2-methyl-6-(methylcarbamoyl)pyrazole-5-carboxanilide Chlorantraniliprole [iso] Chlorantranilipol 3-Bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide Clorantraniliprole Chlorantraniliprole 35%WDG Chlorpyrifos benzamide Rynaxypyr|||Chlorantranilipole|||Rynaxpyr Chlorantraniliprole in Acetone Chlorantraniliprole in Methanol Chlorantraniliprole 10.0 μg/ml Acetonitrile Chlorantraniliprole, 10 mM in DMSO Chlorantraniliprole 100 μg/mL in Acetonitrile 500008-45-7 C18H14BrCl2N5O2 pesticide Agro-Products