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Testosterone

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Identification
Molecular formula
C19H28O2
CAS number
58-22-0
IUPAC name
(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
State
State

At room temperature, testosterone is in a solid state.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
435.00
Boiling point (Kelvin)
708.15
General information
Molecular weight
288.42g/mol
Molar mass
288.4240g/mol
Density
1.1200g/cm3
Appearence

Testosterone is typically a white to off-white crystalline powder.

Comment on solubility

Solubility Overview

The compound (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one exhibits some fascinating solubility characteristics that are significant for various applications. Understanding its solubility in different solvents can be crucial for its practical usage.

Solubility Characteristics

  • Solvent Compatibility: This compound is likely to be soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone, which are commonly used in pharmaceutical and chemical industries.
  • Polarity Influence: The presence of hydroxyl (-OH) groups in its structure can enhance solubility in polar solvents, but the overall hydrophobic character from its complex hydrocarbon framework may limit solubility in highly polar water.
  • Temperature Effects: Increased temperature might improve the compound’s solubility in organic solvents, facilitating its use in various chemical reactions.
  • Concentration Factors: At higher concentrations, saturation may occur, which can affect the dissolution rate and overall stability of the solution.

In summary, the solubility of (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one is primarily influenced by the polarity of the solvent and the temperature of the environment. Understanding these factors can greatly enhance the efficacy of this compound in various applications.

Interesting facts

Interesting Facts about 17-Hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

This complex compound, often referred to as a derivative of steroids, exhibits intriguing characteristics that make it significant in various scientific fields. Notable points include:

  • Structural Complexity: The compound features multiple stereocenters which contribute to its enantiomeric diversity. The specific stereochemistry plays a crucial role in its biological activity.
  • Biological Relevance: Like many steroid derivatives, this compound may exhibit interactions with hormonal pathways, potentially impacting various physiological processes.
  • Synthetic Routes: Due to its intricate structure, the synthesis of this compound often involves multiple steps and specific conditions to ensure the correct configuration of all stereocenters.
  • Research Applications: Compounds of this type are commonly investigated for their medicinal properties, including their potential use in treatments for hormonal imbalances and other health conditions.
  • Natural Occurrence: Certain natural sources are known to produce similar compounds, highlighting the significance of studying both natural and synthetic versions for a better understanding of their roles in nature and pharmacology.

The importance of such compounds cannot be overstated, as they not only enhance our understanding of organic chemistry but also pave the way for innovations in medicinal chemistry. In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This validates the exploration of complex compounds like this one, which may lead to groundbreaking discoveries and applications.

Synonyms
Boldenone
Dehydrotestosterone
846-48-0
17beta-Boldenone
1,2-Didehydrotestosterone
1,2-Dehydrotestosterone
delta1-Testosterone
Boldenona
Boldenonum
17beta-Hydroxyandrosta-1,4-dien-3-one
Boldenonum [INN-Latin]
Boldenona [INN-Spanish]
1,4-Androstadien-17beta-ol-3-one
Boldenone [INN:BAN]
17beta-Hydroxyandrosta-1,4-diene-3-one
17-beta-Hydroxyandrosta-1,4-dien-3-one
EINECS 212-686-0
Boldenone (INN)
NSC 79102
5H7I2IP58X
17-beta-Hydroxy-17-alpha-1,4-androstadien-3-one
CHEBI:34584
BOLDENONE [INN]
BOLDENONE [MI]
Androsta-1,4-dien-3-one, 17beta-hydroxy-
DTXSID20894201
EC 212-686-0
ANDROSTA-1,4-DIEN-3-ONE, 17-beta-HYDROXY-
Androsta-1,4-dien-3-one, 17-hydroxy-, (17beta)-
Boldenonum (INN-Latin)
Boldenona (INN-Spanish)
TESTOSTERONE IMPURITY H [EP IMPURITY]
(17beta)-17-hydroxyandrosta-1,4-dien-3-one
1,4-androstadiene-17-beta-ol-3-one
Androsta-1,4-dien-3-one, 17-hydroxy-, (17.beta.)-
TESTOSTERONE IMPURITY H (EP IMPURITY)
DTXCID201324247
Androsta-1,4-dien-3-one, 17beta-hydroxy-(8CI)
Androsta-1,4-dien-3-one, 17-hydroxy-, (17beta)-(9CI)
212-686-0
1-Dehydrotestosterone
NSC-79102
17beta-Hydroxyandrost-1,4-diene-3-one
.DELTA.1-Testosterone
Boldenone (1.0mg/mL in Acetonitrile)
1,4-Androstadien-17.beta.-ol-3-one
17.beta.-Hydroxyandrosta-1,4-dien-3-one
UNII-5H7I2IP58X
17-Hydroxyandrosta-1,4-dien-3-one
17b-Hydroxyandrosta-1,4-dien-3-one
Boldenone; 17beta-Hydroxyandrosta-1,4-dien-3-one; Testosterone Imp. H (EP); Testosterone Impurity H
Boldenone [WHO-DD]
1-Dehydrotestosterone, 8
SCHEMBL15903
(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
CHEMBL209073
BDBM91719
MSK2292
Androsta-1, 17.beta.-hydroxy-
RSIHSRDYCUFFLA-DYKIIFRCSA-N
Boldenone, 1mg/ml in Acetonitrile
NSC79102
LMST02020018
MSK2292-100A
s5225
Boldenone 1.0 mg/ml in Acetonitrile
AKOS005067864
CCG-267343
DB01541
FB156779
Androsta-1, 17-hydroxy-, (17.beta.)-
NS00008511
Boldenone Solution in Acetonitrile, 100ug/mL
Boldenone, VETRANAL(TM), analytical standard
D07536
Q891284
(8R,10R,13S,17S)-17-Hydroxy-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-cyclopenta[a]phenanthren-3-one