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(3-amino-3-carboxy-propyl)-dimethyl-selenonium

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Identification
Molecular formula
C7H16NO2Se
CAS number
144328-47-2
IUPAC name
(3-amino-3-carboxy-propyl)-dimethyl-selenonium
State
State

At room temperature, (3-amino-3-carboxy-propyl)-dimethyl-selenonium is typically a solid. It is often found as part of a complex or in combination with salt ions, giving it a crystalline structure and enhancing its stability in solid form.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
246.15g/mol
Molar mass
246.1500g/mol
Density
1.2200g/cm3
Appearence

(3-amino-3-carboxy-propyl)-dimethyl-selenonium appears as a white to off-white solid that may form crystals. It is usually handled in the form of a salt like a chloride or iodide, which alters its appearance slightly depending on the specific salt.

Comment on solubility

Solubility of (3-amino-3-carboxy-propyl)-dimethyl-selenonium

(3-amino-3-carboxy-propyl)-dimethyl-selenonium is an interesting compound that showcases unique solubility properties. Given its structure, it contains both hydrophilic and hydrophobic elements which greatly influence its solubility profile.

Key Factors Affecting Solubility:

  • Nature of the Selenonium Ion: The positive charge on the selenonium ion contributes to its solubility in polar solvents.
  • Presence of Functional Groups: The amino and carboxy groups are highly polar and can form strong hydrogen bonds with water molecules, enhancing solubility.
  • pH Dependency: The solubility may vary with changes in pH, as the protonation state of the amino group can affect its interaction with solvents.

In general, it can be expected that (3-amino-3-carboxy-propyl)-dimethyl-selenonium will be soluble in polar solvents such as water and alcohols due to the presence of multiple polar functional groups. However, its solubility might decrease in non-polar solvents due to lack of strong interaction. Additionally, one might observe increased solubility at elevated temperatures which can enhance molecular movement and interactions.

To summarize, the solubility of this compound is largely influenced by its charge, functional groups, and environmental conditions:

  1. High solubility in polar solvents.
  2. Potentially reduced solubility in non-polar solvents.
  3. Variable solubility with pH changes.

Understanding the solubility characteristics of this compound can be pivotal for its applications in various chemical processes.

Interesting facts

Interesting Facts about (3-amino-3-carboxy-propyl)-dimethyl-selenonium

(3-amino-3-carboxy-propyl)-dimethyl-selenonium is a fascinating compound that belongs to the class of organoselenium compounds. Here are some captivating insights that showcase its uniqueness:

  • Organoselenium Chemistry: This compound highlights the intriguing role of selenium in organic synthesis. Selenium analogs of sulfur-containing compounds often exhibit enhanced biological activity.
  • Biological Significance: Compounds containing selenium are of great interest in biochemistry. They are known to play crucial roles in various biological processes, including antioxidant mechanisms and the modulation of enzyme functions.
  • Potential Therapeutic Applications: Research indicates that organoselenium compounds may have promising applications in therapeutics, particularly in cancer treatment and as anti-inflammatory agents. Their ability to interact with cellular pathways makes them a topic of interest in drug design.
  • Complexity of Structure: The structure of (3-amino-3-carboxy-propyl)-dimethyl-selenonium features an amino group and a carboxyl group, which can participate in various biochemical reactions, enhancing its versatility in synthetic applications.
  • Environmental Impact: Selenium compounds, while beneficial in small amounts, can be toxic in higher concentrations. Understanding the properties and behaviors of such compounds helps scientists assess their environmental impact and safety.
  • Research Opportunities: Given its unique characteristics, this compound presents numerous opportunities for research and experimentation in both synthetic and medicinal chemistry.

In conclusion, (3-amino-3-carboxy-propyl)-dimethyl-selenonium represents a bridge between inorganic and organic chemistry, illuminating the significant role of selenium in various fields. As ongoing research continues to uncover its potential applications, this compound serves as a reminder of the complexities and capabilities of chemical compounds in our world.

Synonyms
(3-AMINO-3-CARBOXYPROPYL)DIMETHYLSELENONIUM
7728-97-4
(3-amino-3-carboxypropyl)-dimethylselanium
(3-Amino-3-carboxypropyl)(dimethyl)selanium
Se-Methylselenomethionine
Se-methyl selenomethionine
Se-methyl-selenomethionine
DTXSID50998524
CHEBI:156246
(3-amino-3-carboxypropyl)dimethylselanium
(3-amino-3-carboxypropyl)(dimethyl)selenonium