Skip to main content

3,4-Methylenedioxyamphetamine

ADVERTISEMENT
Identification
Molecular formula
C10H13NO4
CAS number
4764-17-4
IUPAC name
2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid
State
State

At room temperature, 3,4-Methylenedioxyamphetamine is generally found as a solid. It can exist as a powder or crystals, which are then often pressed into pills or capsules for distribution. Its solid form is typical for amphetamine derivatives.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
179.21g/mol
Molar mass
179.2110g/mol
Density
1.2000g/cm3
Appearence

3,4-Methylenedioxyamphetamine (MDA) appears as a white or off-white crystalline powder. It can also be found in the form of small crystals or a pressed tablet. In its pure form, it typically has a slightly bitter taste. The compound is often distributed in tablet or capsule form, where the appearance may vary depending on additional substances that are included as fillers or binding agents.

Comment on solubility

Solubility of 2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid

The solubility of 2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid can be influenced by several factors, leading to intriguing characteristics:

  • Polarity: This compound contains polar functional groups, which typically enhances solubility in polar solvents such as water.
  • pH Sensitivity: The acidic nature of the compound can affect its solubility. At different pH levels, ionization may occur, influencing its solubility in aqueous solutions.
  • Hydrogen Bonding: The presence of nitrogen and oxygen atoms allows for potential hydrogen bonding with solvents, further increasing its solubility in compatible mediums.
  • Solvent Compatibility: While soluble in polar solvents, solubility may decrease in nonpolar environments. Therefore, using a solvent that fits the compound's structure is crucial.

As a guiding principle, it’s essential to consider that, “like dissolves like.” Thus, understanding the interactions between 2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid and various solvents can lead to effective solubility outcomes in practical applications.

Interesting facts

Exploring 2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid

2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid, often referred to as a member of the amino acid family, presents a captivating molecular structure that bridges the realms of organic chemistry and biochemistry. This compound is characterized by its unique combination of an amino group and a carboxylic acid functional group, which is typical for amino acids. However, the addition of the benzodioxole moiety adds intriguing properties, influencing its interactions and biological roles.

Key Characteristics:

  • Functional Versatility: As an amino acid derivative, this compound serves as a building block in peptide synthesis, opening doors for the development of novel pharmaceuticals.
  • Biological Implications: The presence of the benzodioxole structure suggests potential links to natural products and may hint at neuroactive properties, making it an important subject of study in neuroscience.
  • Synthesis and Reactivity: The preparation of this compound can be achieved through various synthetic methodologies, showcasing the creativity of chemists in constructing complex molecules from simpler precursors.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This compound exemplifies the endless possibilities inherent in organic synthesis. As scientists continue to explore the detailed mechanisms of its biological activities and interactions, who knows what *further* surprises await in the realms of pharmacology and molecular science?

To sum up, 2-(1,3-benzodioxol-5-ylmethylamino)propanoic acid is not just an ordinary compound; it represents the intersections of *chemical innovation*, *biological activity*, and *synthetic versatility*, making it a noteworthy subject for both academic research and potential therapeutic applications.

Synonyms
N-Piperonylalanine
ALANINE, N-PIPERONYL-
3201-30-7
BRN 1318649
Propionic acid, 2-(3,4-methylenedioxybenzylamino)-
NSC86378
SCHEMBL19326700
DTXSID90953894
NSC-86378
N-[(2H-1,3-Benzodioxol-5-yl)methyl]alanine
17834-19-4