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Testosterone acetate

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Identification
Molecular formula
C23H32O4
CAS number
1045-69-8
IUPAC name
(17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate
State
State

At room temperature, testosterone acetate is typically in a solid state, specifically a crystalline powder form.

Melting point (Celsius)
137.00
Melting point (Kelvin)
410.15
Boiling point (Celsius)
496.30
Boiling point (Kelvin)
769.45
General information
Molecular weight
330.47g/mol
Molar mass
330.4670g/mol
Density
1.1500g/cm3
Appearence

Testosterone acetate appears as a white or almost white crystalline powder. It is often described as odorless or having a faint odor.

Comment on solubility

Solubility of (17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate

The solubility of the compound C23H32O4, known as (17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate, exhibits characteristics typical for compounds of similar structure. While specific solubility data might not be readily available, we can make some educated observations based on its molecular features.

Factors Affecting Solubility

  • Molecular Weight: With a molecular weight of 372.50 g/mol, larger molecules may generally exhibit lower solubility in water.
  • Polarity: The presence of functional groups (like the ester group) suggests some degree of polarity, which can influence solubility in polar solvents.
  • Hydrophobic Character: The large hydrocarbon framework contributes to hydrophobicity, typically leading to lower solubility in water.

In general, one might expect this compound to be:

  1. Soluble in Organic Solvents: Likely soluble in non-polar organic solvents such as hexane or ether due to its hydrophobic characteristics.
  2. Insoluble in Water: The predominant hydrophobic structure suggests that it would have limited solubility in polar solvents like water.
  3. Moderate Solubility in Polar Organic Solvents: It may exhibit some solubility in polar organic solvents, such as ethanol or acetone, where both polar and non-polar interactions can occur.

In summary, while the exact solubility can vary based on environmental conditions and derivations, the characteristics of the compound suggest a predominantly non-polar solubility profile, emphasizing the importance of solvent choice when working with such compounds.

Interesting facts

Interesting Facts about 17-Acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) Acetate

This remarkable compound belongs to a class of chemicals known for their diverse biological activities and structural complexity. Here are some fascinating insights about this particular acetate:

  • Natural Origins: Many compounds similar to this acetate are derived from natural sources, particularly in the realm of steroids and hormones, highlighting the intricate relationship between natural products and synthetic chemistry.
  • Biological Activities: Acetates often serve as prodrugs, which means they can be converted into active forms within biological systems, making them incredibly important in pharmaceutical research.
  • Structural Complexity: The extensive hydrocarbon framework, combined with the presence of functional groups like the acetyl and ketone groups, renders this molecule an excellent subject for studies in stereochemistry and conformational analysis.
  • Potential Applications: Compounds of this type are often investigated for their potential applications in drug development, particularly in targeting specific biological pathways or mimicking natural hormones.

As chemists delve deeper into the properties and functionalities of 17-acetyl-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl acetate, they uncover endless possibilities for innovation in medicinal chemistry and beyond. The structural intricacies and diverse effects of such compounds offer a thrilling avenue for discovery in the ever-evolving field of chemical science.

Synonyms
Aragest
17-Hydroxy-6-methylpregn-4-ene-3,20-dione 17-acetate
SCHEMBL14262777
BDBM86680
PSGAAPLEWMOORI-UHFFFAOYSA-N
(6S,8R,9S,10R,13S,14S,17R)-17-Acetyl-6,10,13-trimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate
162462-70-6
CAS_4042
NSC_4042
LS-15067
SY077009
A19457
Pregn-4-ene-3,20-dione, 17-(acetyloxy)-6-(methyl-d3)-, (6alpha)-