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Tramadol

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Identification
Molecular formula
C16H25NO1
CAS number
27203-92-5
IUPAC name
9-(2-amino-1-methyl-ethyl)fluoren-9-ol
State
State

At room temperature, tramadol is in a solid state. It is usually found in the form of tablets or capsules for medical use due to its analgesic properties.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
376.20
Boiling point (Kelvin)
649.35
General information
Molecular weight
263.38g/mol
Molar mass
263.3840g/mol
Density
1.2230g/cm3
Appearence

Tramadol is a white, crystalline powder. It is typically odorless and has a bitter taste. The compound is often encountered in pharmaceutical preparations as a hydrochloride salt, which is water-soluble.

Comment on solubility

Solubility of 9-(2-amino-1-methyl-ethyl)fluoren-9-ol

The solubility of 9-(2-amino-1-methyl-ethyl)fluoren-9-ol can be influenced by various factors, including its molecular structure and the presence of functional groups. This compound contains both aromatic and amino functionalities, which play a significant role in its solubility profile.

Key Points About Solubility:

  • The amino group typically increases the hydrophilicity of the compound, enhancing its ability to dissolve in polar solvents.
  • Conversely, the hydrophobic fluorenyl moiety may decrease solubility in aqueous solutions.
  • In general, 9-(2-amino-1-methyl-ethyl)fluoren-9-ol is expected to be more soluble in polar organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).
  • It may exhibit limited solubility in non-polar solvents due to its aromatic characteristics.

In conclusion, while the solubility properties of 9-(2-amino-1-methyl-ethyl)fluoren-9-ol might favor polar environments, experimenting with different solvents is essential for optimal dissolution. As always, the specific conditions such as temperature and pH must also be taken into account for precise solubility assessments.

Interesting facts

Interesting Facts About 9-(2-amino-1-methyl-ethyl)fluoren-9-ol

9-(2-amino-1-methyl-ethyl)fluoren-9-ol, a fascinating compound in the realm of organic chemistry, displays intriguing properties and applications that appeal to both chemists and biology enthusiasts alike. Here are some key points about this compound:

  • Structure and Functionality: This compound features a unique fluorene backbone with an amino group substitution. Its structure resembles that of polycyclic aromatic hydrocarbons, which contributes to its potential *fluorescent* properties.
  • Biological Relevance: Compounds like 9-(2-amino-1-methyl-ethyl)fluoren-9-ol often find their place in biochemical studies due to their role as *fluorescent probes*. Such probes can be invaluable in cellular imaging and monitoring biological processes.
  • Photophysical Properties: This compound may exhibit interesting photophysical characteristics, including energy transfer and fluorescence emission at specific wavelengths. Such properties are crucial for applications in the *development of sensors* and *light-emitting devices*.
  • Versatile Applications: Beyond biological imaging, the compound also holds promise in organic electronics, particularly as a material in *OLEDs (Organic Light Emitting Diodes)* and other optoelectronic devices.
  • Synthetic Pathways: The synthesis of 9-(2-amino-1-methyl-ethyl)fluoren-9-ol can lead to various derivatives, enabling researchers to explore *structure-activity relationships*. This is crucial in chemical research for optimizing properties.
  • Regulatory Interest: Due to its structural similarity to other chemical entities, researchers must approach this compound with a *regulatory lens*, considering its environmental and health implications during development and application.

In summary, 9-(2-amino-1-methyl-ethyl)fluoren-9-ol is much more than a simple aromatic compound. Its potential applications in various fields, from biology to materials science, make it a subject of ongoing research and discussion within the scientific community.

Synonyms
SCHEMBL11128737