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: |
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 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 | pka | 12.42±0.70(Predicted) | Stability: | Light Sensitive |
| L 656748 Usage And Synthesis |
Description | Emamectin 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. | Uses | Emamectin 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 |
|