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spinosyn D aglycone

Base Information
  • Chemical Name:spinosyn D aglycone
  • CAS No.:149439-79-2
  • Molecular Formula:C25H36O5
  • Molecular Weight:416.558
  • Hs Code.:
spinosyn D aglycone

Synonyms:

Suppliers and Price of spinosyn D aglycone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Cayman Chemical
  • Spinosyn D aglycone
  • 2.5mg
  • $ 926.00
  • Cayman Chemical
  • Spinosyn D aglycone
  • 500μg
  • $ 285.00
Total 5 raw suppliers
Chemical Property of spinosyn D aglycone
Chemical Property:
  • Boiling Point:641.9±55.0 °C(Predicted) 
  • PKA:14.28±0.70(Predicted) 
  • Density:1.19±0.1 g/cm3(Predicted) 
Purity/Quality:

>95% by HPLC *data from raw suppliers

Spinosyn D aglycone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Spinosyn D aglycone is an acid degradation product produced by hydrolysis of both saccharide groups on spinosyn D, the minor component of the commercial insecticide, Spinosad. Spinosyn D aglycone is only weakly active as an insecticide as the saccharides are considered essential for potent activity. Despite the importance of spinosyns as agro-chemical insecticides and more recently as animal health products, there are few published reports of the biological activity or the levels of spinosyn D aglycone in animals or in the environment.
Technology Process of spinosyn D aglycone

There total 3 articles about spinosyn D aglycone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sulfuric acid; In water; at 80 ℃; for 3.75h; pH=1.7;
DOI:10.7164/antibiotics.51.795
Guidance literature:
Multi-step reaction with 2 steps
1: 42 percent / K2CO3 / methanol / 1 h / 20 °C
2: 63 percent / 1 N H2SO4 / H2O / 3.75 h / 80 °C / pH 1.7
With sulfuric acid; potassium carbonate; In methanol; water; 1: Elimination / 2: Hydrolysis;
DOI:10.7164/antibiotics.51.795
Guidance literature:
Multi-step reaction with 3 steps
1: N-chlorosuccinimide; diisopropyl sulfide / CH2Cl2 / 6.25 h / -78 °C
2: 42 percent / K2CO3 / methanol / 1 h / 20 °C
3: 63 percent / 1 N H2SO4 / H2O / 3.75 h / 80 °C / pH 1.7
With N-chloro-succinimide; diisopropylsulfide; sulfuric acid; potassium carbonate; In methanol; dichloromethane; water; 1: Oxidation / 2: Elimination / 3: Hydrolysis;
DOI:10.7164/antibiotics.51.795
upstream raw materials:

3'-des-O-methyl-3'-keto spinosyn D

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