Malathion 15% + Fenvalerate 5% Ec Insecticide

• Customization: Available
• CAS No.: 121-75-5
• Formula: C10h19o6PS2
• Model NO.: EC
• Appearance: Liquid
• Source: Organic Synthesis
• Toxicity of High and Low: Highly Toxic and High Toxic Drugs
• Mode: Systemic Insecticide
• Toxicological Effect: Nerve Poison
• Transport Package: 25kg Drum
• Specification: TC EC
• Trademark: MOLOTUS
• Origin: China
• HS Code: 3808
• Production Capacity: 5000t

Product Description

Malathion 15% + Fenvalerate 5% EC Insecticide Pesticide

Malathion
Malathion is an insecticide approved for use in the EU and in many other countries. It is moderately soluble in water and readily soluible in many organic solvents. It is quite volatile and has a low potential for leaching to groundwater. Malathion is not usually persistent in soil or water systems. It is moderately toxic to mammals, a cholineserase inhibitor and a neurotoxin. Malathion is highly toxic to honey bees and aquatic species with the exception of algae. It is moderately toxic to birds and earthworms.

Description: An insecticide and acaricide used to control a wide range of pests
Example pests controlled: Coleoptera; Diptera; Hemiptera; Lepidoptera; Mosquitoes; Fruit flies; Aphids; Mealybugs; Leaf hoppers; Spidermites
Example applications: Vegetables including turnips; Public health applications; Ornamental trees and shrubs; Stored produce
Efficacy & activity: -
Availability status: Current

Chemical structure: 

Isomerism	A chiral molecule existing as two enantiomers
Chemical formula	C10H19O6PS2
Canonical SMILES	CCOC(=O)CC(C(=O)OCC)SP(=S)(OC)OC
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	JXSJBGJIGXNWCI-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C10H19O6PS2/c1-5-15-9(11)7-8(10(12)16-6-2)19-17(18,13-3)14-4/h8H,5-7H2,1-4H3

General status: 

Pesticide type	Insecticide, Acaricide, Veterinary substance
Substance group	Organophosphate
Minimum active substance purity	950 g/kg (racemic mixture)
Known relevant impurities	EU dossier - malaoxon <1g/kg, isomalathion <2g/kg, MeOOSPS-triester <15g/kg, MeOOOPS-triester 5g/kg
Substance origin	Synthetic
Mode of action	Broad-spectrum, non-systemic with contact, stomach and respiratory action. Acetylcholinesterase (AChE) inhibitor.
CAS RN	121-75-5
EC number	204-497-7
CIPAC number	12
US EPA chemical code	057701
PubChem CID	4004
Molecular mass (g mol^-1)	330.36

Fenvalerate
Description: An insecticide and acaricide used to control a range of pests especially those with resistance to organochlorine, organophosphate and carbamate insecticides
Example pests controlled: Various insects belongs to the Lepidoptera, Diptera, Orthoptera, Hemiptera, and Coleoptera families, Blackfly, Mosquitoes, Termites
Example applications: Cotton; Soybeans; Various vegetables; Fruit including apples, pears, peaches, grapes; Nuts

Chemical structure: 

Isomerism	A molecule with 2 chiral centres, fenvalerate is a mixture of four optical isomers which have different insecticidal activities. The 2-S alpha (or SS) configuration is the most insecticidally active isomer.
Chemical formula	C25H22ClNO3
Canonical SMILES	CC(C)C(C1=CC=C(C=C1)Cl)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	NYPJDWWKZLNGGM-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C25H22ClNO3/c1-17(2)24(18-11-13-20(26)14-12-18)25(28)30-23(16-27)19-7-6-10-22(15-19)29-21-8-4-3-5-9-21/h3-15,17,23-24H,1-2H3

General status: 

Pesticide type	Insecticide, Acaricide, Termiticide, Veterinary substance
Substance group	Pyrethroid
Minimum active substance purity	92%
Known relevant impurities	-
Substance origin	Synthetic
Mode of action	Non-systemic with contact and stomach action. Sodium channel modulator.
CAS RN	51630-58-1
EC number	257-326-3
CIPAC number	334
US EPA chemical code	109301
PubChem CID	3347
Molecular mass (g mol^-1)	419.90
PIN (Preferred Identification Name)	(E)-cyano(3-phenoxyphenyl)methyl (2E)-2-(4-chlorophenyl)-3-methylbutanoate
IUPAC name	(RS)-α-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate
CAS name	cyano(3-phenoxyphenyl)methyl 4-chloro-α-(1-methylethyl)benzeneacetate
Other status information	Chemical subject to PIC regulations