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L 656748

CAS No.
121124-29-6
Chemical Name:
L 656748
Synonyms
L 656748;EMaMectin B1a;Unii-IX4GP7848F;Avermectin A1a, 5-O-demethyl-4''-deoxy-4''-(methylamino)-, (4''R)-
CBNumber:
CB32703722
Molecular Formula:
C49H75NO13
Molecular Weight:
886.12
MDL Number:
MOL File:
121124-29-6.mol
MSDS File:
SDS
Last updated:2023-05-21 10:59:17

L 656748 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
FDA UNII IX4GP7848F

L 656748 price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 24060 Emamectin B1a ≥99% 121124-29-6 1mg $336 2024-03-01 Buy
Cayman Chemical 24060 Emamectin B1a ≥99% 121124-29-6 5mg $1172 2024-03-01 Buy
Usbiological 448150 Emamectin B1a 121124-29-6 1mg $779 2021-12-16 Buy
TRC E520505 EmamectinB1a 121124-29-6 5mg $1000 2021-12-16 Buy
Product number Packaging Price Buy
24060 1mg $336 Buy
24060 5mg $1172 Buy
448150 1mg $779 Buy
E520505 5mg $1000 Buy

L 656748 Chemical Properties,Uses,Production

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

Raw materials

Preparation Products

L 656748 Suppliers

Global( 20)Suppliers
Supplier Tel Email Country ProdList Advantage
BOC Sciences
16314854226; +16314854226 inquiry@bocsci.com United States 19743 58
Lynnchem 86-(0)29-85992781 17792393971 info@lynnchem.com China 4587 58
Novachemistry 44-20819178-90 02081917890 info@novachemistry.com United Kingdom 4381 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684 sales@rrkchem.com China 56039 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
ShangHai Anpel Co, Ltd. 18501792038; 18501792038 shanpel@anpel.com.cn China 9614 58
Meng Cheng Technology (Shanghai) Co., LTD 400-820-6829 sales@mitachieve.com China 8864 58
Energy Chemical 021-58432009 400-005-6266 marketing1@energy-chemical.com China 44843 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.com China 24246 58

121124-29-6(L 656748)Related Search:

EMaMectin B1a L 656748 Avermectin A1a, 5-O-demethyl-4''-deoxy-4''-(methylamino)-, (4''R)- Unii-IX4GP7848F 121124-29-6