Emamectin Benzoate 10% + Indoxacarb 8% Wp

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

Product Description

Insecticide Pesticide Emamectin Benzoate 10% + Indoxacarb 8% WP


Emamectin Benzoate
Application
Non-systemic insecticide which penetrates leaf tissues by translaminar movement. Paralyses the Lepidoptera, which stop feeding within hours of ingestion, and die 2-4 dat. For control of Lepidoptera such as armyworm, bollworm, cutworm, cole moth, cabbage caterpillar, Mite, Prodenia litura (Fabricius) and so on harmful insects in many kinds of crops including vegetables, fruit, brassicas, cotton, tobacco and pine trees.

 

Product name	Emamectin benzoate
General info	Function: Insecticide
	MF: C49H77NO13
	CAS: 137512-74-4
	High effective agrochemical
Toxicology	Oral Acute oral LD50 for rats 76-89 mg/kg.  Skin and eye Acute dermal LD50 for rabbits >2000 mg/kg.  It is not irritant to skin, and has no sensitising potential. Inhalation LC50 (4 h) for rats 2. 12-4. 44 mg/m3.  NOEL (1 y) for dogs 0. 25 mg/kg b. W. ADI 0. 0025 mg/kg. Other Not tumorigenic. Toxicity class WHO (a. I. ) II Birds Acute oral LD50 for mallard ducks 46, bobwhite quail 264 mg/kg. Dietary LC50 (8 d) for mallard ducks 570, bobwhite quail 1318 ppm. Fish LC50 (96 h) for rainbow trout 174, sheepshead minnow 1430 G/l. Daphnia LC50 0. 99? G/l. Algae >94? G/l. Bees Toxic to bees. Worms >1000 mg/kg.
Applications	Harmful insects on the tobacco, the tea, the cotton, fruit tree . Red belt cacaecia crataegan, Smoke aphis noctuid, Tobacco chaerocampa oldenlandiae, Cabbage moth, Sticks the insect, Cutworm moth, Cabbage butterfly, Vegetable heart snout moth, Wooden scoop insect

Indoxacarb
Description: An insecticide for use on a wide range of crops to control certain Lepidoptera, cockroaches and ants
Example pests controlled: Beet armyworm, Fire ants; Cockroaches
Example applications: Cotton; Brassicas; Sweet corn; Lettuce; Fruiting vegetables; Fruit including apples, pears, cherries

Chemical structure: 

Isomerism	A chiral molecule, existing in the R- and S-forms but normally used as the S-stereosomer
Chemical formula	C22H17ClF3N3O7
Canonical SMILES	COC(=O)C12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl
Isomeric SMILES	COC(=O)[C@]12CC3=C(C1=NN(CO2)C(=O)N(C4=CC=C(C=C4)OC(F)(F)F)C(=O)OC)C=CC(=C3)Cl
International Chemical Identifier key (InChIKey)	VBCVPMMZEGZULK-NRFANRHFSA-N
International Chemical Identifier (InChI)	InChI=1S/C22H17ClF3N3O7/c1-33-18(30)21-10-12-9-13(23)3-8-16(12)17(21)27-28(11-35-21)19(31)29(20(32)34-2)14-4-6-15(7-5-14)36-22(24,25)26/h3-9H,10-11H2,1-2H3/t21-/m0/s1

General status: 

Pesticide type	Insecticide
Substance group	Oxadiazine
Minimum active substance purity	930 g/kg
Known relevant impurities	EU 2017 dossier - 4,4'-methylenebis(N,N-diethylaniline < 0.0025 g/kg
Substance origin	Synthetic
Mode of action	Contact and stomach action. Voltage-dependent sodium channel blocker.
CAS RN	173584-44-6
EC number	-
CIPAC number	612
US EPA chemical code	118200
PubChem CID	107720
Molecular mass (g mol^-1)	527.83
PIN (Preferred Identification Name)	methyl (S)-N-[7-chloro-2,3,4a,5-tetrahydro-4a-(methoxycarbonyl)indeno[1,2-e][1,3,4]oxadiazin-2-ylcarbonyl]-4'-(trifluoromethoxy)carbanilate
IUPAC name	methyl (S)-N-[7-chloro-2,3,4a,5-tetrahydro-4a-(methoxycarbonyl)indeno[1,2-e][1,3,4]oxadiazin-2-ylcarbonyl]-4'-(trifluoromethoxy)carbanilate
CAS name	methyl (4aS)-7-chloro-2,5-dihydro-2-(((methoxycarbonyl)(4-(trifluoromethoxy)phenyl)amino])carbonyl)indeno(1,2-e)(1,3,4)oxadiazine-4a(3H)-carboxylate