87585-03-3 Usage
Description
6α-Hydroxy Norgestrel, also known as 6α-Hydroxy Levonorgestrel, is a hydroxylated impurity of Norgestrel. It is a synthetic progestin that is structurally similar to the naturally occurring hormone progesterone. 6α-Hydroxy Norgestrel is used as an impurity reference standard for the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
6α-Hydroxy Norgestrel is used as an impurity reference standard for the quality control and analysis of Norgestrel-containing pharmaceutical products. It helps ensure the purity, potency, and safety of these medications.
Used in Research and Development:
6α-Hydroxy Norgestrel is used as a research compound to study the effects of hydroxylation on the pharmacological properties of Norgestrel. This can provide valuable insights into the development of new progestin-based drugs with improved efficacy and safety profiles.
Used in Quality Control Testing:
6α-Hydroxy Norgestrel is used as a reference material in the development and validation of analytical methods for the detection and quantification of impurities in Norgestrel-containing pharmaceuticals. This helps maintain the quality and consistency of these products throughout their manufacturing and distribution processes.
Check Digit Verification of cas no
The CAS Registry Mumber 87585-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,8 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87585-03:
(7*8)+(6*7)+(5*5)+(4*8)+(3*5)+(2*0)+(1*3)=173
173 % 10 = 3
So 87585-03-3 is a valid CAS Registry Number.
87585-03-3Relevant articles and documents
ELECTROOXIDATIVE SIMULATION OF STEREOSELECTIVITY IN MICROSOMAL ALLYLIC HYDROXYLATION
Shono, Tatsuya
, p. 91 - 94 (2007/10/02)
A comparison of the stereochemistry of liver microsomal γ-hydroxylation of some cyclic α,β-unsaturated ketones with that of electrochemical γ-acetoxylation of the corresponding dienol esters and with that of peracid oxidation of the dienol esters has been carried out.
