3-O-Methyl-3-methoxymaxterone
3-O-Methyl-3-methoxymaxterone
CAS: 92282-70-7
Molecular Formula: C21H36O3
3-O-Methyl-3-methoxymaxterone - Names and Identifiers
| Name | 3-O-Methyl-3-methoxymaxterone |
| Synonyms | 3,3-Dimethoxyandrostan-17β-ol 3-O-Methyl-3-methoxymaxterone Androstan-17-ol, 3,3-dimethoxy-, (5α,17β)- (9CI) |
| CAS | 92282-70-7 |
3-O-Methyl-3-methoxymaxterone - Physico-chemical Properties
| Molecular Formula | C21H36O3 |
| Molar Mass | 336.52 |
| Density | 1.07±0.1 g/cm3(Predicted) |
| Boling Point | 416.3±15.0 °C(Predicted) |
| Appearance | Powder |
| pKa | 15.04±0.70(Predicted) |
| Storage Condition | 2-8℃ |
3-O-Methyl-3-methoxymaxterone - Introduction
3-O-Methyl-3-methoxymaxterone(3-O-Methyl-3-methoxymaxterone) is a synthetic androgen analog. It has the molecular formula C21H36O3 and a molecular weight of 336.5G/mole.
Properties: 3-o-methyll-3-methoxymaxterone is a crystalline solid that is readily soluble in organic solvents such as chloroform and dichloromethane. It is stable at room temperature.
Purpose: Due to its structural similarity to androgens, 3-O-Methyl-3-methoxymaxterone is widely used in medical research to explore the mechanism of androgen receptor action and potential drug development. In addition, it has been abused in the sports world as a banned substance to improve the performance of athletes.
Preparation Method: A commonly used preparation method is by chemical synthesis. The specific steps include methyl formate esterification reaction for androdione, followed by reduction, formate hydrolysis and methyl esterification reaction, and finally purification to obtain the target product.
Safety Information: Given that 3-O-Methyl-3-methoxymaxterone is similar to androgens, abusive use may have serious health consequences. It is listed as a banned substance by many sports organizations and competitive bodies. Under normal circumstances, it should not be used in humans, and the relevant experimental procedures should be carried out under the guidance of trained personnel. There is still a lack of sufficient research on the toxicity, carcinogenicity and other information related to human health. When using and handling this substance, please follow safe operating procedures and strictly control its use and analysis.
Properties: 3-o-methyll-3-methoxymaxterone is a crystalline solid that is readily soluble in organic solvents such as chloroform and dichloromethane. It is stable at room temperature.
Purpose: Due to its structural similarity to androgens, 3-O-Methyl-3-methoxymaxterone is widely used in medical research to explore the mechanism of androgen receptor action and potential drug development. In addition, it has been abused in the sports world as a banned substance to improve the performance of athletes.
Preparation Method: A commonly used preparation method is by chemical synthesis. The specific steps include methyl formate esterification reaction for androdione, followed by reduction, formate hydrolysis and methyl esterification reaction, and finally purification to obtain the target product.
Safety Information: Given that 3-O-Methyl-3-methoxymaxterone is similar to androgens, abusive use may have serious health consequences. It is listed as a banned substance by many sports organizations and competitive bodies. Under normal circumstances, it should not be used in humans, and the relevant experimental procedures should be carried out under the guidance of trained personnel. There is still a lack of sufficient research on the toxicity, carcinogenicity and other information related to human health. When using and handling this substance, please follow safe operating procedures and strictly control its use and analysis.
Last Update：2024-04-09 18:58:34
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CAS: 92282-70-7
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CAS: 92282-70-7
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View History
3-O-Methyl-3-methoxymaxterone
{[1-(甲氧基甲基)环丙基]甲基}胺
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头孢唑兰酸
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{[1-(甲氧基甲基)环丙基]甲基}胺
17767-94-1
(S)-3-AMINO-4-(4-NITROPHENYL)BUTANOIC ACID
2-OXO-CLOPIDOGREL
头孢唑兰酸
乙二胺四乙酸三钠浓缩液