Skip to main content

Testosterone benzoate

ADVERTISEMENT
Identification
Molecular formula
C25H30O3
CAS number
572-67-4
IUPAC name
(17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) benzoate
State
State

At room temperature, testosterone benzoate is in solid form, usually found as a powder.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
384.53g/mol
Molar mass
384.5390g/mol
Density
1.1000g/cm3
Appearence

Testosterone benzoate is a white or off-white crystalline powder.

Comment on solubility

Solubility of (17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) benzoate (C25H30O3)

The solubility of (17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) benzoate is influenced by several factors, including its molecular structure and interactions with solvents. Here are key points regarding its solubility:

  • Hydrophobic Characteristics: Due to its largely hydrocarbon-based structure, the compound exhibits hydrophobic properties, which may limit its solubility in polar solvents like water.
  • Non-Polar Solvents: It is likely to have better solubility in non-polar organic solvents such as hexane, toluene, and chloroform, which can stabilize its hydrophobic regions.
  • Temperature Dependence: Solubility typically increases with temperature; thus, warming the solvent may enhance the dissolution of this compound.
  • pH Influence: The solubility may also change with pH levels, specifically if the compound can ionize or alter its charge state in different pH environments.

In conclusion, the solubility of C25H30O3 is crucial for its applications, and understanding the interplay of molecular structure and solvent characteristics is essential for predicting its behavior in various environments.

Interesting facts

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

This compound, often referred to in the realm of organic synthesis and medicinal chemistry, represents a fascinating intersection of steroid chemistry and aromatic functionalities. Here are some engaging facts about this compound:

  • Structural Complexity: The compound contains a decahydrocyclopenta[a]phenanthrene core, showcasing intricate rings that are characteristic of many natural steroid frameworks. This complexity not only adds to the challenge of synthesis but also opens up possibilities for diverse biological activities.
  • Biological Relevance: Derivatives of compounds similar to this one are often studied for their potential therapeutic applications, particularly in the fields of oncology and endocrinology. Their ability to interact with hormone receptors is a topic of ongoing research.
  • Synthetic Pathways: The synthesis of this compound can involve multiple steps, often utilizing strategies such as **ring-closing metathesis** or **stereoselective reductions** to achieve the desired stereochemistry and functional groups.
  • Functional Groups: The presence of the benzoate moiety suggests potential roles in molecular recognition and reactivity, which chemists find intriguing for applications in drug design and delivery systems.
  • Research Potential: Studies utilizing this compound may focus not only on its synthetic utility but also on its pharmacological properties, which could lead to the development of new agents for treating various conditions.

Finally, it is fascinating to note that compounds like this serve as a reminder of the vast potential locked within organic molecules. The exploration of their properties and functionalities is crucial for advancing our understanding of both chemistry and its applications in medicine.

Synonyms
(17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl) benzoate
Estra-1,3,5(10)-triene-3,17-diol (17beta)-, 3-benzoate
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, 3-benzoate
17-hydroxyestra-1,3,5(10)-trien-3-yl benzoate
Oestradiolbenzat
Spectrum_001199
SpecPlus_000911
Spectrum2_001096
Spectrum3_001168
Spectrum4_000591
Spectrum5_001159
Oprea1_381937
BSPBio_002755
KBioGR_001082
KBioSS_001679
DivK1c_007007
SPBio_001172
CHEMBL430289
SCHEMBL12187133
CHEBI:91653
KBio1_001951
KBio2_001679
KBio2_004247
KBio2_006815
KBio3_002255
UYIFTLBWAOGQBI-UHFFFAOYSA-N
HMS2092J19
BBL028505
CCG-40258
MFCD00003692
STL146316
AKOS005720769
NCGC00178488-01
SY038941
VS-08804
SBI-0051680.P002
1,3,5(10)-estratriene-3,17b-diol 3-benzoate
3-Benzoyloxy-17beta-hydroxyestra-1,3,5(10)-triene
BRD-A36066264-001-02-3
BRD-A36066264-001-03-1
1-hydroxy-11a-methyl-1H,2H,3H,3aH,3bH,4H,5H,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-yl benzoate
896441-79-5