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Testosterone acetate

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Identification
Molecular formula
C23H32O4
CAS number
1045-69-8
IUPAC name
(3-acetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) acetate
State
State
At room temperature, testosterone acetate is typically a solid. It is stable and maintains its structure as a crystalline powder under standard conditions.
Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
377.00
Boiling point (Kelvin)
650.15
General information
Molecular weight
388.58g/mol
Molar mass
388.5780g/mol
Density
1.1380g/cm3
Appearence

Testosterone acetate typically appears as a white to creamy white crystalline powder. It is odorless and is known for its solid crystalline structure, which indicates high purity and well-defined crystalline properties.

Comment on solubility

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

The solubility of the compound with the formula C23H32O4 can be an intriguing topic for discussion. This compound, characterized by its complex structure, tends to exhibit unique solubility properties. Below are some key points to consider:

  • Polarity: The presence of acetate groups indicates that this compound has polar characteristics, which might allow it to dissolve in polar solvents.
  • Hydrophobicity: The large hydrocarbon structure suggests significant hydrophobic regions, which can enhance solubility in non-polar solvents like hexane or chloroform.
  • Solvent Compatibility: It may show solubility in a range of organic solvents but could present limited solubility in water due to its hydrophobic nature.
  • Temperature Dependency: As with many organic compounds, solubility often increases with temperature; therefore, examining solubility at varying temperatures could yield additional insights.

In general, while the exact solubility of this specific compound may require experimental determination, one can highly anticipate that its solubility characteristics will be affected by both its functional groups and overall molecular structure. Remember, as the old adage goes, “Like dissolves like,” which is a fundamental principle to guide the exploration of its solubility in different solvents.

Interesting facts

Interesting Facts About (3-acetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) Acetate

This intriguing compound represents a significant structure in organic chemistry, characterized by its complex arrangement of multiple rings and functional groups. Here are some fascinating insights about it:

  • Complex Structure: The compound features a decahydrocyclopenta[a]phenanthren core, which is notable for its multi-cyclic framework. Such structures often exhibit unique chemical properties, making them valuable in various applications.
  • Biological Relevance: Compounds related to this structure are often studied in the context of steroidal hormones. The presence of acetoxy functional groups can influence biological activity, which is pertinent in pharmacology.
  • Synthesis Potential: The synthesis of complex organic compounds like this one demonstrates the creativity and precision required in modern synthetic organic chemistry. Pathways to synthesize such molecules often involve advanced techniques in synthetic strategies.
  • Applications in Research: Researchers utilize this compound in the study of receptor interactions, assessing its potential as a therapeutic agent or a lead compound for drug development.
  • Historical Significance: The study of related compounds has illuminated our understanding of hormonal functions and paved the way for advancements in medical treatments, particularly in the fields of endocrinology and oncology.

In summary, (3-acetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) acetate serves as an excellent example of the intricacies found in organic compounds and their substantial impact across various scientific fields.

Synonyms
Estradiol, diacetate
estradiol diacetate
17beta-EstradiolDiacetate
3434-88-6
.beta.-Estradiol diacetate
beta-Estradiol diacetate
17.beta.-Estradiol diacetate
Estradiol-3,17.beta.-diacetate
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, diacetate
NSC-106559
estra-1,3,5(10)-triene-3,17-diyl diacetate
Estradiol, diacetate (8CI)
MLS002695914
CHEMBL1713935
beta -Estradiol 3,17-diacetate
VQHQLBARMFAKSV-UHFFFAOYSA-N
NSC106559
SMR001562105
Estra-1,5(10)-triene-3,17-diol (17.beta.)-, diacetate