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• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid methyl esters
• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acid esters Fatty acid methyl esters

Dimethyl 3-aminopentanedioate Hydrochloride: An Overview of CAS No. 77313-10-1

Dimethyl 3-aminopentanedioate hydrochloride (CAS No. 77313-10-1) is a versatile compound with significant applications in various fields, particularly in pharmaceutical and chemical research. This compound is a derivative of aminopentanedioic acid, which has been extensively studied for its potential therapeutic properties and chemical reactivity. The addition of dimethyl groups and the hydrochloride salt form enhances its solubility and stability, making it a valuable intermediate in the synthesis of more complex molecules.

The chemical structure of Dimethyl 3-aminopentanedioate hydrochloride consists of a central five-carbon backbone with an amino group and two carboxylic acid groups, both of which are esterified with methyl groups. The presence of the hydrochloride salt form ensures that the compound is highly soluble in water, which is crucial for its use in aqueous reactions and biological systems. This unique combination of functional groups provides a platform for a wide range of chemical transformations and biological interactions.

In recent years, there has been growing interest in the use of Dimethyl 3-aminopentanedioate hydrochloride as a building block for the synthesis of novel pharmaceuticals. One notable area of research involves its application in the development of drugs targeting neurodegenerative diseases. Studies have shown that compounds derived from aminopentanedioic acid can modulate specific neurotransmitter systems, potentially offering new therapeutic avenues for conditions such as Alzheimer's disease and Parkinson's disease.

Beyond its pharmaceutical applications, Dimethyl 3-aminopentanedioate hydrochloride has also found use in the field of materials science. Its ability to form stable complexes with various metals has led to its exploration as a ligand in coordination chemistry. Researchers have demonstrated that these complexes exhibit unique optical and electronic properties, making them promising candidates for applications in sensors, catalysts, and advanced materials.

The synthesis of Dimethyl 3-aminopentanedioate hydrochloride typically involves several steps, starting with the preparation of the corresponding acid or ester. One common approach is to react aminopentanedioic acid with methanol in the presence of an acid catalyst to form the dimethyl ester. The resulting ester is then converted to the hydrochloride salt by treatment with hydrogen chloride gas or a concentrated solution of hydrochloric acid. This synthetic route is well-documented and can be readily adapted to large-scale production processes.

In terms of safety and handling, Dimethyl 3-aminopentanedioate hydrochloride is generally considered safe when proper precautions are taken. However, as with any chemical compound, it is important to follow standard laboratory practices to ensure safe handling and storage. The compound should be stored in a cool, dry place away from incompatible materials, and appropriate personal protective equipment (PPE) should be used during handling.

The environmental impact of Dimethyl 3-aminopentanedioate hydrochloride is another important consideration. While it is not classified as a hazardous substance under current regulations, it is essential to dispose of any waste products responsibly to minimize potential environmental impact. Many laboratories have implemented green chemistry principles to reduce waste generation and promote sustainable practices in chemical synthesis.

In conclusion, Dimethyl 3-aminopentanedioate hydrochloride (CAS No. 77313-10-1) is a multifaceted compound with a wide range of applications in pharmaceutical research, materials science, and chemical synthesis. Its unique chemical structure and properties make it an invaluable tool for scientists working in these fields. As research continues to advance, it is likely that new applications and insights will emerge, further highlighting the importance of this compound in modern science.

• 77856-53-2((3S)-3-amino-5-methoxy-5-oxopentanoic acid)
• 1086106-57-1(methyl (3S)-3-aminopentanoate)
• 139243-55-3((S)-3-Amino-butyric acid methyl ester hydrochloride)
• 88598-13-4(Pentanedioic acid, 3-amino-, monomethyl ester)
• 60793-95-5(Diethyl 3-aminopentanedioate)
• 77313-09-8(Dimethyl 3-aminopentanedioate)
• 1345983-89-2(Dimethyl 3-aminopentanedioate acetate)
• 532435-35-1(methyl (3R)-3-aminopentanoate hydrochloride)
• 833453-79-5(Octanoic acid, 3-amino-, methyl ester, (3S)-)
• 139243-54-2((R)-Methyl 3-aminobutanoate hydrochloride)