abamectin 1.8% EC made in China manufacturer best quality in China

La description

NOMENCLATURE

Common name abamectin (BSI, draft E-ISO, ANSI); abamectine ((f) draft F-ISO)

IUPAC name (*0E,*4E,*6E,*2Z)-(1R,4S,5'S,6S,6'R,8R,*2S,*3S,*0R,*1R,*4S)*6'-[(S)-sec-butyl]**1,**-dihydroxy*5',*1,*3,**-tetramethyl**-oxo*3,7,**-trioxatetracyclo[*5.6.1.*4,8.**0,*4]pentacosa**0,*4,*6,**-tetraene**-spiro*2'-(5',6'-dihydro*2'H-pyran)***-yl 2,*-dideoxy**-O-(2,*-dideoxy**-O-methyl-a-L-arabino-hexopyranosyl)**-O-methyl-a-L-arabino-hexopyranoside (i) mixture with (*0E,*4E,*6E,*2Z)-(1R,4S,5'S,6S,6'R,8R,*2S,*3S,*0R,*1R,*4S)**1,**-dihydroxy*6'-isopropyl*5',*1,*3,**-tetramethyl**-oxo*3,7,**-trioxatetracyclo[*5.6.1.*4,8.**0,*4]pentacosa**0,*4,*6,**-tetraene**-spiro*2'-(5',6'-dihydro*2'H-pyran)***-yl 2,*-dideoxy**-O-(2,*-dideoxy**-O-methyl-a-L-arabino-hexopyranosyl)**-O-methyl-a-L-arabino-hexopyranoside (ii) (4:1)  

Chemical Abstracts name *-O-demethylavermectin A1a (i) mixture with *-O-demethyl***-de(*-methylpropyl)***-(*-methylethyl)avermectin A1a (ii)  

Other names avermectin B1  CAS RN [*********2] (abamectin); [*********3] (i); [*********4] (ii)  EEC no. ********3 (avermectin B1a); ********9 (avermectin B1b)  Development codes MK****6 (Merck & Co.); C***6 (Ciba); L***6,**3  

 

 

 

APPLICATIONS

Biochemistry Acts by stimulating the release of g-aminobutyric acid, an inhibitory neurotransmitter, thus causing paralysis. See M. J. Turner & J. M. Schaeffer in Ivermectin and Abamectin, W. C. Cambell ed., Springer-Verlag, New York (***9) p. *3.  Mode of action Insecticide and acaricide with contact and stomach action. Has limited plant systemic activity, but exhibits translaminar movement.  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 *8 g/ha for mite control, *1 to *2 g/ha for control of leaf miners. Also used for control of fire ants. Phytotoxicity May be phytotoxic to pome fruit when mixed with captan.  Formulation types EC.  Compatibility Not compatible with captan.  

 

ANALYSIS

Product analysis by hplc with u.v. detection. Residues by conversion to a fluorescent product followed by hplc with fluorescence detection. See T. Wehner et al. in Comp. Anal. Profiles, Chapt. 4.  

 

MAMMALIAN TOXICOLOGY

Reviews FAO/WHO *4, *0, *2 (see part 2 of the Bibliography). G. Lankas & L. R. Gordon in Toxicology in Ivermectin and Abamectin, W. C. Campbell ed., Springer-Verlag (***9) pp. *****2.  Oral Acute oral LD*0 (in sesame oil) for rats *0, mice *3.6 mg/kg; (in water) for rats **1 mg/kg.  Skin and eye Acute percutaneous LD*0 for rabbits >***0 mg/kg. Mild eye irritant; non-irritating to skin (rabbits).  ADI (JMPR) 0.**2 mg/kg b.w. [***7] (for sum of abamectin and 8,*-Z- isomer); 0.**1 mg/kg b.w. [***5] (for residues not containing D*8,*-isomer).  Other Non-mutagenic in the Ames test.  Toxicity class EPA (formulation) IV  

 

ECOTOXICOLOGY

鸟类 野鸭急性经口LD*0 *4.6，短尾鹌鹑>***0 mg/kg。鱼 LC*0 （*6 h） 虹鳟鱼 3.2，蓝鳃翻车鱼 9.6 mg/l。水蚤 EC*0 （*8 h） 0.*4 ppb。藻类（*2 小时）用于 Pseudokirchneriella subcapitata >**0 mg/l。其他水生属 LC*0 （*6 h） 粉红虾 （Panaeus duorarum） 1.6，蓝蟹 （Callinectes sapidus） **3 ppb。蜜蜂 对蜜蜂有毒。蠕虫 LC*0 （*8 d） 用于蚯蚓 *8 mg/kg 土壤。

 

环境命运

动物 快速消除（*6 小时内 *****0%），主要通过粪便排出;尿排泄量为 0.**1.4%。植物 三种不同植物中的每一种的降解/代谢都是相似的，主要通过植物表面的光解发生。因此，残基的定义表示为阿维菌素 B1 及其 8,*-Z-阿维菌素 B1 光异构体的组合残基。土壤/环境 与土壤紧密结合，被土壤微生物迅速降解。无生物蓄积。