6α-Hydroxy Norgestrel

Base Information

Chemical Name:6α-Hydroxy Norgestrel
CAS No.:87585-03-3
Molecular Formula:C₂₁H₂₈O₃
Molecular Weight:328.452
Hs Code.:
Mol file:87585-03-3.mol

Synonyms:(6α,17α)-13-Ethyl-6,17-dihydroxy-18,19-dinorpregn-4-en-20-yn-3-one

Suppliers and Price of 6α-Hydroxy Norgestrel

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

TRC
6α-HydroxyLevonorgestrel
10mg
$ 1390.00

Total 9 raw suppliers

Chemical Property of 6α-Hydroxy Norgestrel

Chemical Property:

PSA：57.53000
LogP:2.85340
Storage Temp.:-20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly, Heated), Ethyl Acetate (Sparingly)

Purity/Quality:

97% ^*data from raw suppliers

6α-HydroxyLevonorgestrel ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 6α-Hydroxy Levonorgestrel (Levonorgestrel EP Impurity G) is a hydroxylated impurity of Norgestrel (N689500).

Technology Process of 6α-Hydroxy Norgestrel

There total 2 articles about 6α-Hydroxy Norgestrel 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:

Reference yield:

: 797-63-7
levonorgestrel

: 87585-03-3
(6S,8R,9S,10R,13S,14S,17R)-13-Ethyl-17-ethynyl-6,17-dihydroxy-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one

: 55555-97-0
13β-ethyl-17α-ethynyl-6β,17β-dihydroxy-4-en-3-one

Guidance literature:: at 37 ℃; for 0.166667h; in incubation mixture, with rat liver microsomes; or perbenzoic acid oxidation of dienol acetate;
DOI:10.1016/S0040-4039(01)91156-6