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Testosterone acetate

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Identification
Molecular formula
C21H30O3
CAS number
1045-69-8
IUPAC name
(13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) acetate
State
State

At room temperature, testosterone acetate is a solid. It is generally stored in a cool, dry place and can be handled as a powder.

Melting point (Celsius)
139.00
Melting point (Kelvin)
412.15
Boiling point (Celsius)
430.50
Boiling point (Kelvin)
703.65
General information
Molecular weight
330.46g/mol
Molar mass
330.4610g/mol
Density
1.1700g/cm3
Appearence

Testosterone acetate typically appears as a white or creamy white crystalline powder. This substance is usually provided as a powder due to its easy handling and enhanced stability in this form. Testosterone acetate may have a mild odor.

Comment on solubility

Solubility of (13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) acetate

The solubility of the compound (13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) acetate (C21H30O3) can be influenced by several factors. Here are some key points to consider:

  • Polarity: The presence of the acetate functional group contributes to the compound's overall polarity, which can enhance its solubility in polar solvents such as water.
  • Non-polar regions: The hydrophobic (non-polar) carbon structures can hinder solubility in water, making the compound more soluble in organic solvents like ethanol, methanol, or chloroform.
  • Temperature effects: Generally, increasing the temperature tends to improve solubility for most compounds; thus, this compound may see enhanced dissolution at elevated temperatures.
  • Concentration: At higher concentrations, solubility can vary due to the saturation point, potentially leading to precipitation.

In summary, solubility is complex and can be dependent on a combination of factors including solvent choice, temperature, and concentration. Understanding these interactions is crucial for predicting the behavior of C21H30O3 in different environments.

Interesting facts

Exploring 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl Acetate

The compound 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl acetate is a fascinating molecule with significant implications in the fields of biochemistry and pharmacology. As a member of the steroid family, it exhibits unique structural features that are of great interest to scientists.

Key Features and Uses

  • Hormonal Activity: This compound's structure plays a critical role in its potential function as a steroid, which can interact with hormonal pathways in the body.
  • Natural Products: Its synthetic analogs often mimic natural steroid hormones, making it valuable in the development of hormonal therapies.
  • Chemical Synthesis: Researchers often study the synthesis methods involved in creating such complex molecules, leading to discoveries of more efficient pathways for similar compounds.

Scientific Significance

The investigation of 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl acetate not only provides insight into steroid chemistry but also enhances our understanding of biological processes, including:

  • Cell Signaling: Investigating how this compound interacts with receptors can reveal much about cell signaling pathways.
  • Drug Development: Its structure can inspire the creation of new pharmaceuticals targeting various health conditions influenced by steroid hormones.

In summary, the compelling structure and potential applications of 13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl acetate make it a noteworthy subject for ongoing scientific research. Its role in understanding hormonal mechanisms and developing therapeutic agents cannot be overstated, highlighting the importance of such compounds in advancing both medicine and chemistry.

Synonyms
estrone acetate
Estrone, acetate
901-93-9
(13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) acetate
DivK1c_000518
CHEMBL5485679
SCHEMBL20006536
HMS501J20
KBio1_000518
NINDS_000518
AKOS030240929
IDI1_000518
DB-057187
11a-methyl-1-oxo-2H,3H,3aH,3bH,4H,5H,9bH,10H,11H-cyclopenta[a]phenanthren-7-yl acetate