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Methoxyphenamine Hydrochloride

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Identification
Molecular formula
C11H15NO3 · HCl
CAS number
10312-36-6
IUPAC name
5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid;hydrochloride
State
State

At room temperature, Methoxyphenamine hydrochloride is in a solid state. It is commonly found in laboratory settings as a reagent or an intermediate.

Melting point (Celsius)
208.00
Melting point (Kelvin)
481.15
Boiling point (Celsius)
362.00
Boiling point (Kelvin)
635.15
General information
Molecular weight
229.67g/mol
Molar mass
229.6670g/mol
Density
1.3600g/cm3
Appearence

Methoxyphenamine hydrochloride typically appears as a white to off-white crystalline powder. It is often used in its pure form for chemical analysis and synthesis.

Comment on solubility

Solubility of 5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid; hydrochloride

The solubility of 5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid; hydrochloride in various solvents can be influenced by several factors, including temperature, pH, and the presence of other solutes. Here are some key points regarding its solubility:

  • Water Solubility: This compound is generally soluble in water due to the presence of hydrophilic functional groups, such as the amino and carboxy groups.
  • Organic Solvents: It is less soluble in non-polar organic solvents. For example, solvents like hexane or toluene may not effectively dissolve this compound.
  • Temperature Dependence: As with many ionic compounds, rising temperatures may enhance its solubility in water.
  • pH Influence: The solubility can also be affected by pH levels; at acidic or basic conditions, the ionization of the carboxylic and amino groups can alter solubility.

In summary, 5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid; hydrochloride showcases good solubility in polar solvents like water while exhibiting limited solubility in non-polar media, thus making it essential for applications where an aqueous medium is proposed.

Interesting facts

Interesting Facts about 5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid; hydrochloride

This compound is a fascinating example of a drug that has important implications in the field of pharmacology. Known for its role in biological systems, it serves as a valuable tool for research and therapeutic applications.

Key Characteristics:

  • Biological Activity: The compound is recognized for its ability to interact with various biological targets, which makes it of particular interest in drug development.
  • Structure: Its unique molecular structure, featuring both an amine and a carboxylic acid group, allows for effective interactions within biological environments.
  • Research Applications: Scientists often employ this compound in studies aimed at understanding metabolic pathways and enzyme activity.

Chemical Attributes:

  • Potential Applications: The drug may have applications in treating conditions associated with metabolic dysregulation.
  • Analogues: Researchers frequently explore analogues of this compound to enhance its efficacy and reduce potential side effects.
  • Environmental Impact: Studies on the degradation and environmental persistence of the compound are vital for evaluating its ecological safety.

In summary, 5-(2-amino-2-carboxy-ethyl)-2-methoxy-benzoic acid; hydrochloride is not only a compound of theoretical interest but also a practical tool in the laboratory that bridges the gap between chemistry and biology. It exemplifies the quest for new therapeutic agents derived from organic chemistry.

Synonyms
3641-44-9
DL-alpha-Amino-3-carboxy-4-methoxy-hydrocinnamic acid hydrochloride
DL-3-Carboxy-4-methoxyphenylalanine hydrochloride
Alanine, 3-carboxy-4-methoxyphenyl-, hydrochloride, DL-
HYDROCINNAMIC ACID, alpha-AMINO-3-CARBOXY-4-METHOXY-, HYDROCHLORIDE, DL-
DTXSID50957757
3-Carboxy-O-methyltyrosine--hydrogen chloride (1/1)