L 656748

L 656748 Suppliers list
Company Name: BOC Sciences
Tel: 16314854226; +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:Emamectin B1a
CAS:121124-29-6
Purity:>99% by HPLC Remarks:BOC Sciences also provides custom synthesis services for Emamectin B1a.
Company Name: Lynnchem  
Tel: 86-(0)29-85992781 17792393971
Email: info@lynnchem.com
Products Intro: Product Name:L 656748
CAS:121124-29-6
Purity:>99% by HPLC Package:1mg;5mg
Company Name: Novachemistry  
Tel: 44-20819178-90 02081917890
Email: info@novachemistry.com
Products Intro: Product Name:Emamectin B1a
CAS:121124-29-6
Purity:>99% by HPLC Package:1mg;5mg
Company Name: Shenzhen Polymeri Biochemical Technology Co., Ltd.  
Tel: +86-400-002-6226 13028896684
Email: sales@rrkchem.com
Products Intro: Product Name:Emamectin B1a
CAS:121124-29-6
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:Emamectin B1a
CAS:121124-29-6
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
L 656748 Basic information
Product Name:L 656748
Synonyms:EMaMectin B1a;L 656748;Avermectin A1a, 5-O-demethyl-4''-deoxy-4''-(methylamino)-, (4''R)-;Unii-IX4GP7848F;Avermectin impurity 17 monomer
CAS:121124-29-6
MF:C49H75NO13
MW:886.12
EINECS:
Product Categories:
Mol File:121124-29-6.mol
L 656748 Structure
L 656748 Chemical Properties
Boiling point 935.0±65.0 °C(Predicted)
density 1.21±0.1 g/cm3(Predicted)
storage temp. Store at -20°C, protect from light
solubility DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
form A solid
pka12.42±0.70(Predicted)
Stability:Light Sensitive
Safety Information
MSDS Information
L 656748 Usage And Synthesis
DescriptionEmamectin B1a is a semisynthetic derivative of avermectin B1a . It binds to GABAA receptors (Ki = 17.6 nM in rat brain membranes), including those containing β1, β2, or β3 subunits (IC50s = 57, 210, and 49.8 nM for α1β1γ2, α1β2γ2, and α1β3γ2 subunits, respectively), and potentiates the GABA response. Emamectin B1a also binds to and inhibits glycine receptors (IC50 = 218 nM in rat spinal cord). Emamectin B1a induces mortality in 90% of S. exigua larvae in a diet incorporation assay at a dose of 1.067 ng/ml, which is approximately 1,500-fold more toxic than avermectin B1. It is effective against neonate S. eridania larvae in a foliage spray bioassay and when applied topically.
UsesEmamectin B1a is a semi-synthetic 4”-epimethylamino analogue of avermectin B1a prepared by oxidation of the 4”-hydroxy moiety and reductive amination. The introduction of the methylamino group greatly enhances the insecticidal potency of the avermectin class. Emamectin B1a, as a benzoate salt, is the major component (>90%) of the commercial insecticide/acaricide, emamectin. Members of the avermectin/milbemycin class exert their insecticidal/anthelmintic effects by binding to glutamate-gated chloride channels expressed on nematode neurones and pharyngeal muscle cells.
L 656748 Preparation Products And Raw materials
Tag:L 656748(121124-29-6) Related Product Information
EMaMectin B1b