α-Amino-β-methylaminopropionic Acid Hydrochloride

Base Information

• Chemical Name: α-Amino-β-methylaminopropionic Acid Hydrochloride
• CAS No.: 20790-76-5
• Molecular Formula: C4H11ClN2O2
• Molecular Weight: 154.597
• Hs Code.: 2923900090
• Mol file: 20790-76-5.mol

Synonyms:2-Amino-3-(methylamino)propanoic acid hydrochloride;3-(Methylamino)-DL-alanine hydrochloride;3-(MethylaMino)-DL-alanine Monohydrochloride

Chemical Property of α-Amino-β-methylaminopropionic Acid Hydrochloride

Chemical Property:

• Melting Point: 185-187°C
• PSA: 75.35000
• LogP: 0.51090
• Storage Temp.: Hygroscopic, -20?C Freezer, Under Inert Atmosphere
• Solubility.: Water (Slightly)

Purity/Quality:

98%Min ^*data from raw suppliers

α-Amino-β-methylaminopropionicAcidHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: α-Amino-β-methylaminopropionic Acid is an amino acid isolated from the seeds of Cycas Circinalis that is neurotoxic to higher animals. α-Amino-β-methylaminopropionic Acid may cause Guam disease, a form of amyotrophic lateral sclerosis (ALS). α-Amino-β-methylaminopropionic Acid is reported to be an agonist at the metabotropic glutamate receptor. An amino acid isolated from the seeds of Cycas Circinalis that is neurotoxic to higher animals. May cause Guam disease, a form of amyotrophic lateral sclerosis (ALS). Reported to an agonist at the metabotropic glutamate receptor.

Technology Process of α-Amino-β-methylaminopropionic Acid Hydrochloride

There total 1 articles about α-Amino-β-methylaminopropionic Acid Hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

N-Acetamidoacrylic acid (5429-56-1) + methylamine (74-89-5) → DL-2-amino-3-(N-methylamino)propionic acid monohydrochloride (20790-76-5)

Guidance literature:

With hydrogenchloride; Multistep reaction; 1.) water, 40 deg C, 72 h, 2.) water, reflux, 5 h;

Reference yield:

DL-2-amino-3-(N-methylamino)propionic acid monohydrochloride (20790-76-5) → piruvate (57-60-3) + methylamine (74-89-5)

Guidance literature:

With KOH buffer pH=8.0; L-methyonine γ-lyase; N-[tris(hydroxymethyl)methyl]glycine; pyridoxal 5'-phosphate; In water; at 37 ℃; for 0.166667h;

upstream raw materials:

N-Acetamidoacrylic acid

methylamine

Downstream raw materials:

piruvate

methylamine

Refernces