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Testosterone acetate

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Identification
Molecular formula
C21H30O3
CAS number
1045-69-8
IUPAC name
[2-(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] acetate
State
State

At room temperature, testosterone acetate is typically in a solid state. It is often found as a powder.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.00
Boiling point (Celsius)
468.60
Boiling point (Kelvin)
741.80
General information
Molecular weight
330.47g/mol
Molar mass
330.4670g/mol
Density
1.1294g/cm3
Appearence

Testosterone acetate is a white to off-white crystalline powder. It has very low solubility in water.

Comment on solubility

Solubility of [2-(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl] acetate

The solubility of the compound C21H30O3 can be quite intricate to assess given its complex structure. Influenced by both its hydrophobic and hydrophilic regions, solubility in various solvents will vary significantly. Here are some key considerations:

  • Hydrophobic Character: The large hydrophobic cyclopenta[a]phenanthrene moiety tends to reduce solubility in polar solvents like water.
  • Hydrophilic Functional Groups: The presence of acetate and keto groups can enhance solubility in organic solvents and some non-polar environments.
  • Temperature Dependence: Solubility can increase with temperature, making it more soluble in warm organic solvents.

The overall solubility of this compound may be described as:

  • Low in water: Due to the predominance of non-polar structural features.
  • Moderate in organic solvents: Solubility may be favorable in solvents like ethanol or chloroform.

In summary, this chemical has a challenging solubility profile, often requiring specific solvents to achieve satisfactory dissolution. Understanding these nuances is crucial for practical applications where solubility plays a critical role.

Interesting facts

Interesting Facts about 2-(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl acetate

This intriguing organic compound is a fascinating example of structural complexity within the realm of chemical compounds. Its composition suggests a unique relationship with both biological and synthetic applications.

Chemical Structure and Characteristics

The compound is characterized by:

  • Unique Dodecahydrocyclopenta[a]phenanthrene Backbone: The extensive framework observed in its structure indicates potential interactions with biological systems, notably in steroid synthesis and related fields.
  • Multiple Carbonyl Groups: The presence of two ketone functionalities makes this compound an interesting subject for studies on reactivity and synthesis, particularly in the context of organic chemistry.
  • Acetate Functional Group: This group can impart distinct esterase behavior, making the compound vital in enzymatic processes and synthetic organic reactions.

Potential Applications

Given its structural attributes, this compound could have several practical applications:

  1. Pharmaceutical Chemistry: The compound may serve as a precursor or intermediate in the synthesis of bioactive molecules, potentially leading to novel therapeutics.
  2. Research in Synthetic Biology: Its structure provides a basis for further exploration into steroid-like compounds, which play significant roles in hormonal function.
  3. Material Science: The compound may also find its place in material sciences, offering insights into the synthesis of polymers with unique properties.

Conclusion

The structural complexity and unique functionalities present in this compound make it a valuable subject for ongoing research. As we delve deeper into its properties and potential applications, 2-(10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl acetate stands out as a prime candidate for innovations in various fields of chemistry.

Synonyms
Decorton
Descotone
Desocort
Syncort
3,20-Dioxopregn-4-en-21-yl acetate
Decsterone
Percorten acetate
Corticosterone, acetate
Deoxycorticosterone acetate?
Oprea1_235801
SCHEMBL1021137
21-Hydroxyprogesterone, acetate
NSC9567
VPGRYOFKCNULNK-UHFFFAOYSA-N
BCP31890
Pregn-4-ene-3, 21-(acetyloxy)-
STL503549
AKOS032955001
Pregn-4-ene-3, 21-hydroxy-, acetate
DB-015382
NS00079744
WLN: L E5 B666 OV MUTJ A F FV1OV1
1-Deoxycorticosterone acetate; DOC acetate; Percotol; Cortexone acetate