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Testosterone acetate

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Identification
Molecular formula
C21H30O3
CAS number
1045-69-8
IUPAC name
(1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate
State
State

At room temperature, testosterone acetate is a solid, specifically a crystalline powder. It is typically stable when kept in the right conditions, away from direct light and moisture.

Melting point (Celsius)
137.00
Melting point (Kelvin)
410.15
Boiling point (Celsius)
138.30
Boiling point (Kelvin)
411.45
General information
Molecular weight
330.46g/mol
Molar mass
330.4620g/mol
Density
1.0800g/cm3
Appearence

Testosterone acetate is a white to off-white crystalline powder. It lacks any significant odor and often appears in a fine powdered form, making it easy to handle and process in laboratory settings.

Comment on solubility

Solubility of (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate: C21H30O3

The solubility of (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate can be influenced by several key factors:

  • Polarity: This compound contains both non-polar hydrocarbon segments and a polar acetate functional group. As a result, it has limited solubility in water, which is a polar solvent.
  • Solvent Type: The compound is more likely to dissolve in non-polar or slightly polar organic solvents such as hexane, chloroform, or ether. Its solubility may increase in these environments due to favorable interactions with solvent molecules.
  • Temperature: Solubility can also vary with temperature. Generally, increasing the temperature can enhance solubility in non-polar solvents, making the compound more likely to dissolve.
  • Impurities: The presence of impurities or other solutes can affect the solubility as well, sometimes through phenomena like co-solvency or competition for solvent molecules.

To summarize, one could quote that "solubility is not merely a property but an intricate dance of interactions." Thus, the solubility of C21H30O3 is best observed in non-polar organic media where it exhibits improved dissolution characteristics, while it remains largely insoluble in polar solvents like water.

Interesting facts

Interesting Facts about (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate

This complex compound, commonly referred to in the realm of organic chemistry, showcases the intricate nature of molecular structures. Here are some fascinating insights that every chemistry enthusiast should know:

  • Steroidal Backbone: The presence of a dodecahydrocyclopenta[a]phenanthrene framework indicates that this compound is likely steroidal in nature, which is significant given the enormous biological relevance of steroids.
  • Functional Groups: The inclusion of the acetate group (–OCOCH3) suggests that this compound can participate in various chemical reactions such as esterification and hydrolysis, making it versatile in synthetic applications.
  • Natural Occurrence: Compounds with similar structures may be found in plants and animals, hinting at potential effects on biological systems. For instance, many steroids play crucial roles in hormone regulation.
  • Pharmaceutical Applications: The structural characteristics of this compound may imply that it could have potential as a lead compound for drug discovery, particularly in fields focusing on endocrine functions and therapies.
  • Complexity in Synthesis: The synthesis of such a multi-functionalized compound can be both challenging and exciting, often involving several steps that require precision and a deep understanding of organic reactions.

In the world of organic chemistry, the study of compounds like this one emphasizes not only the diversity of chemical structures but also their potential implications in biological systems and pharmacology. As one might say in the field, "The beauty of chemistry lies not just in its complexity, but in its capability to solve real-world problems." This compound may very well embody that truth!

Synonyms
metenolone acetate
(1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate
Premobolan
Primobolone
Primonabol
SH 567a
Primobolan Tablets
Testosterone, 1-dehydro-4,5.alpha.-dihydro-1-methyl-, acetate
5.alpha.-Androst-1-en-3-one, 17.beta.-hydroxy-1-methyl-, acetate
PGAUJQOPTMSERF-UHFFFAOYSA-N
AKOS015961059
AC-12723
DB-051077
NS00076685
17.beta.-Hydroxy-1-methyl-5.alpha.-androst-1-en-3-one 17-acetate