(6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one

(6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one - Names and Identifiers

Name	(6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one
Synonyms	6A-HYDROXYNORETHINDRONE 6Α-HYDROXY NORETHINDRONE Norethindrone 6-alpha-Hydroxy Impurity (6α,17β)-17-Ethynyl-6,17-dihydroxyestr-4-en-3-one (6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one (6A,17BETA)-6,17-DIHYDROXY-19-NORPREGN-4-EN-20-YN-3-ONE (6S,8R,9S,10R,13S,14S,17R)-17-ethynyl-6,17-dihydroxy-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
CAS	438244-33-8

(6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one - Physico-chemical Properties

Molecular Formula	C20H26O3
Molar Mass	314.42
Storage Condition	2-8°C

(6α,17α)-6,17-Dihydroxy-19-norpregn-4-en-20-yn-3-one - Introduction

(6α,17α)-6, also known as (6α,17α)-6, is a synthetic steroid compound. It has the following properties:

1. Appearance: White crystalline solid.
2. Molecular formula: C20H26O3
3. Molecular weight: 314.42g/mol
4. Melting Point: 161-166 ° C
5. Solubility: slightly soluble in ethanol, almost insoluble in water.

(6α,17α)-6, commonly used in pharmaceutical and chemical laboratories, and has the following uses:

1. Biological Research: as an agonist or inhibitor of progesterone receptor and estrogen receptor.
2. Pharmaceutical industry: for synthetic drugs and steroid compounds.

Its preparation method is generally carried out through the following steps:

1. First, use synthetic chemistry to convert appropriate starting materials (such as progesterone) into target compounds through several reactions.
2. Add appropriate reagents and solvents in the reaction to control the reaction conditions and product purity.
3. The product was purified by filtration and crystallization and identified by a suitable assay.

Regarding its safety information, the following matters need to be noted:

1. Because it belongs to the field of chemical laboratory and medicine, the safe use and operation of the compound need to comply with laboratory safety procedures.
2. Avoid skin contact and inhalation to avoid allergic reactions or toxic effects.
3. Wear appropriate personal protective equipment, such as lab gloves and goggles, when using or handling the compound.
4. It is best to operate in a well-ventilated laboratory environment to avoid its vapor accumulation and harm to the human body.

Last Update：2024-04-09 21:32:49