Phoxim 30% + Fenvalerate 5% Ec Insecticide

• CAS No.: C9h11cl3no3PS
• Formula: 14816-18-3
• Appearance: Liquid
• Source: Organic Synthesis
• Toxicity of High and Low: Highly Toxic and High Toxic Drugs
• Mode: Systemic Insecticide
• Model NO.: EC
• Toxicological Effect: Nerve Poison
• Transport Package: 25kg Drum
• Specification: TC EC
• Trademark: MOLOTUS
• Origin: China
• HS Code: 3808
• Production Capacity: 5000t

Product Description

  Phoxim 30% + Fenvalerate 5% EC Insecticide Pesticide


Phoxim
Description: An insecticide and acaricide used to control stored-product pests such as ants and some soil insects. Also used as a disinfectant.
Example pests controlled: Locusts; lepidopterous larvae; Caterpillars
Example applications: Potatoes; Cotton; Maize; Sugarbeet

Chemical structure: 

Isomerism	Isomeric
Chemical formula	C12H15N2O3PS
Canonical SMILES	CCOP(=S)(OCC)ON=C(C#N)C1=CC=CC=C1
Isomeric SMILES	CCOP(=S)(OCC)O/N=C(\C#N)/C1=CC=CC=C1
International Chemical Identifier key (InChIKey)	ATROHALUCMTWTB-WYMLVPIESA-N
International Chemical Identifier (InChI)	InChI=1S/C12H15N2O3PS/c1-3-15-18(19,16-4-2)17-14-12(10-13)11-8-6-5-7-9-11/h5-9H,3-4H2,1-2H3/b14-12+

General status: 

Pesticide type	Insecticide, Other substance , Veterinary substance
Other constituent type	Disinfectant
Substance group	Organophosphate
Minimum active substance purity	-
Known relevant impurities	-
Substance origin	Synthetic
Mode of action	Non-systemic with contact and stomach action. Short activity period. Acetylcholinesterase (AChE) inhibitor.
CAS RN	14816-18-3
EC number	238-887-3
CIPAC number	364
US EPA chemical code	598800
PubChem CID	9570290
Molecular mass (g mol^-1)	298.3
PIN (Preferred Identification Name)	-
IUPAC name	O,O-diethyl α-cyanobenzylideneaminooxyphosphonothioate
CAS name	4-ethoxy-7-phenyl-3,5-dioxa-6-aza-4-phosphaoct-6-ene-8-nitrile 4-sulphide
Other status information	OSPAR soc

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
Efficacy & activity: -
Availability status: Current

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
2D structure diagram/image available?	Yes

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