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12-epi-Napelline

Base Information
  • Chemical Name:12-epi-Napelline
  • CAS No.:110064-71-6
  • Molecular Formula:C22H33NO3
  • Molecular Weight:359.509
  • Hs Code.:
12-epi-Napelline

Synonyms:(20R)-21-Ethyl-4-methyl-16-methylene-7α,20-cycloveatchane-1α,12β,15β-triol;12-Epinapelline;12-epi-Napelline;Epinapelline, 12-

Suppliers and Price of 12-epi-Napelline
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
  • Usbiological
  • 12-epinapelline
  • 20mg
  • $ 581.00
  • ChemScene
  • 12-Epinapelline
  • 5mg
  • $ 303.00
  • ChemScene
  • 12-Epinapelline
  • 10mg
  • $ 514.00
  • Biorbyt Ltd
  • 12-epinapelline 98%
  • 20 mg
  • $ 591.60
  • Biorbyt Ltd
  • 12-epinapelline 98%
  • 10 mg
  • $ 499.80
  • AvaChem
  • 12-Epinapelline
  • 20mg
  • $ 349.00
  • AvaChem
  • 12-Epinapelline
  • 10mg
  • $ 249.00
  • AvaChem
  • 12-Epinapelline
  • 5mg
  • $ 149.00
  • AvaChem
  • 12-Epinapelline
  • 1mg
  • $ 69.00
  • Arctom
  • 12-Epinapelline
  • 20mg
  • $ 288.00
Total 30 raw suppliers
Chemical Property of 12-epi-Napelline
Chemical Property:
  • Boiling Point:537.8±50.0 °C(Predicted) 
  • PKA:14.30±0.70(Predicted) 
  • PSA:63.93000 
  • Density:1.29±0.1 g/cm3 (20 ºC 760 Torr) 
  • LogP:1.72970 
Purity/Quality:

99%, *data from raw suppliers

12-epinapelline *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 12-?Epinapelline is a diterpene alkaloid which displays anaesthetic activity as toxic neurological agents. Similar to aconitine, its suggested that modulation of voltage gated Na+ channels are responsible for these observations.
Technology Process of 12-epi-Napelline

There total 4 articles about 12-epi-Napelline 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 sodium tetrahydroborate; In methanol; at 20 - 50 ℃; for 4h;
DOI:10.1007/BF00600832
Guidance literature:
With potassium hydroxide; In methanol; water;
DOI:10.1248/cpb.39.1644
Guidance literature:
Lucidusculin 1, LiAlH4;
DOI:10.1139/v74-341
upstream raw materials:

12-epi-lucidusculine

songorine

Downstream raw materials:

liangshanine

C42H55NO5Si

C37H43NO5

C36H41NO5

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