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Nanjing Essence Fine-Chemical Co., Ltd.

Acetamiprid 10% + Abamectin 1% SL, Acetamiprid + Abamectin SL, Acetamiprid + Abamectin manufacturer / supplier in China, offering Acetamiprid 10% + Abamectin 1% SL, Highly Effective Imidacloprid + Thiram (25%+10%Fs), Highly Effective Propiconazole + Difenoconazole (25%+25% Ec) and so on.

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Supplier Homepage Product Insecticide Acetamiprid 10% + Abamectin 1% SL

Acetamiprid 10% + Abamectin 1% SL

FOB Price: Get Latest Price
Min. Order: 1 liter
Production Capacity: 50000 Kl Per Year
Transport Package: 1g-25kg for Liquid Formulations
Payment Terms: L/C, T/T, D/P

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Basic Info
  • Model NO.: SL
  • Source: Organic Synthesis
  • Mode: Contact Insecticide
  • Formulation Types: SL
  • CAS2: 160430-64-8
  • CAS4: 65195-55-3
  • Trademark: Essence
  • Origin: China
  • Appearance: Liquid
  • Toxicity of High and Low: Low Toxicity of Reagents
  • Toxicological Effect: Nerve Poison
  • CAS1: 135410-20-7
  • CAS3: 71751-41-2
  • CAS5: 65195-56-4
  • Specification: 10% + 1% SL
  • HS Code: 3808
Product Description
Acetamiprid 10% + Abamectin 1% SL

Acetamiprid 

NOMENCLATURE
Common name acétamipride ((m) F-ISO); acetamiprid (BSI, E-ISO)  
IUPAC name (E)-N1-[(6-chloro-3-pyridyl)methyl]-N2-cyano-N1-methylacetamidine
Chemical Abstracts name (E)-N-[(6-chloro-3-pyridinyl)methyl]-N′-cyano-N-methylethanimidamide  
CAS RN [135410-20-7]; [160430-64-8] unspecified stereochemistry 
 
Acetamiprid  APPLICATIONS
Acetamiprid  Biochemistry Agonist of the nicotinic acetylcholine receptor, affecting the synapses in the insect central nervous system.

Acetamiprid  Mode of action Systemic insecticide with translaminar activity and with contact and stomach action.

Acetamiprid Uses Control of Hemiptera, especially aphids, Thysanoptera and Lepidoptera, by soil and foliar application, on a wide range of crops, especially vegetables, fruit and tea. Applied at 75-300 g/ha on vegetables, 100-700 g/ha in orchards.

Abamectin NOMENCLATURE
Common name abamectin (BSI, E-ISO, ANSI); abamectine ((f) F-ISO)  
IUPAC name (10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-6′-[(S)-sec-butyl]-21,24-dihydroxy-5′,11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside (i) mixture with (10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-21,24-dihydroxy-6′-isopropyl-5′,11,13,22-tetramethyl-2-oxo-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside (ii) (4:1)
Chemical Abstracts name 5-O-demethylavermectin A1a (i) mixture with 5-O-demethyl-25-de(1-methylpropyl)-25-(1-methylethyl)avermectin A1a (ii)  Other names avermectin B1
CAS RN [71751-41-2] abamectin; [65195-55-3] (i); [65195-56-4] (ii) 


Abamectin APPLICATIONS
Abamectin Biochemistry Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels. See M. J. Turner & J. M. Schaeffer in Ivermectin and Abamectin, p. 73.

Abamectin Mode of action Insecticide, acaricide and nematicide with contact and stomach action. Has limited plant systemic activity, but exhibits translaminar movement.

Abamectin Uses Control of motile stages of mites, leaf miners, suckers, Colorado beetles, etc. on ornamentals, cotton, citrus fruit, pome fruit, nut crops, vegetables, potatoes, and other crops. Application rates are 5.6 to 28 g/ha for mite control, 11 to 22 g/ha for control of leaf miners. Also used for control of nematodes by seed treatment, and of fire ants. Phytotoxicity May be phytotoxic to pome fruit when mixed with captan.

Abamectin Compatibility Not compatible with captan. 
 
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