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Testosterone acetate

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Identification
Molecular formula
C21H30O3
CAS number
1045-69-8
IUPAC name
(17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate
State
State

At room temperature, testosterone acetate is typically found in a solid state. It is a white or almost white powder.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.00
Boiling point (Celsius)
411.30
Boiling point (Kelvin)
684.30
General information
Molecular weight
330.46g/mol
Molar mass
330.4610g/mol
Density
1.0800g/cm3
Appearence

Testosterone acetate appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of (17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate

The solubility characteristics of (17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate can be quite intricate due to its complex structure. Here are some key points regarding its solubility:

  • Solubility in Organic Solvents: This compound is expected to have good solubility in non-polar and weakly polar organic solvents such as dichloromethane, chloroform, and ethyl acetate.
  • Limited Solubility in Water: Based on its large hydrophobic regions and limited polar functional groups, the solubility in water is likely to be very low. This is because water tends to dissolve polar or ionic substances, while organic compounds with large hydrocarbon chains are typically hydrophobic.
  • Influence of Acetyl Group: The presence of an acetyl group may enhance some solubility in polar organic solvents like ethanol, but overall, the compound's predominant hydrophobic characteristics will limit its solubility.

In general, understanding the solubility of such complex structures is critical for applications in various fields, including pharmaceuticals and materials science. As such, empirical solubility testing is often necessary to determine precise solubility behavior under specific conditions.

Interesting facts

Interesting Facts about (17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate

This compound, belonging to the class of steroids, showcases remarkable structural features and biological significance. Here are some captivating insights into this unique chemical:

  • Structure and Configuration: The presence of multiple methyl groups, specifically at positions 10 and 13, along with the acetyl functional group at position 17, contributes to its unique properties. This complex structure highlights the diversity found within steroidal compounds.
  • Biological Relevance: Many steroids share similar frameworks, making them crucial in biological systems. They often serve as hormones, influencing numerous physiological processes, from metabolism to immune responses.
  • Therapeutic Potential: Compounds like this might exhibit potential as therapeutic agents, particularly in the fields of endocrinology or oncology, where steroid analogs can play a role in treatment modalities.
  • Historical Importance: The study of such steroidal compounds has paved the way for significant advances in medicine, influencing the development of steroid therapies and synthetic derivatives.
  • Compound Identification: Given its intricate structure, the identification and synthesis of this compound require advanced techniques, often involving modern analytical methods \(e.g., NMR and mass spectrometry\).

In summary, (17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate stands out not only for its complex configuration but also for its potential implications in various biological applications. As research continues to evolve, compounds like this may lead to new discoveries in both medicinal and pharmaceutical realms.

Synonyms
20-Oxopregn-5-en-3-yl acetate
(17-acetyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl) acetate
Antofin
Artivis
Enescorb
Previsone
Sharmone
1093959-59-1
Pregenolone acetate
14-acetyl-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl acetate
Pregnenolone-3-acetate
1-acetyl-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-yl acetate
Pregn-5-en-20-one, 3.beta.-hydroxy-, acetate
Pregn-5-en-20-one, 3-(acetyloxy)-, (3.beta.)-
MFCD00003627
NCGC00160652-02
NCIOpen2_008303
SCHEMBL670748
Pregn-5-en-20-one, acetate
DTXSID20859678
NSC64827
BBL028112
CCG-56424
STK061707
AKOS000490892
AKOS016352316
NCGC00160652-01
17-acetyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate
SY057216
VS-08669
NS00014008
VU0494344-1
SR-01000645380
SR-01000645380-1
SR-01000645380-2
F1443-0925