L-Aspartic acid-15N

Base Information

• Chemical Name: L-Aspartic acid-15N
• CAS No.: 3715-16-0
• Molecular Formula: C₄H₇NO₄
• Molecular Weight: 134.097
• Hs Code.: 28459000
• European Community (EC) Number: 685-844-3
• Mol file: 3715-16-0.mol

Synonyms:L-Aspartic acid-15N;3715-16-0;L-Asparticacid-15N;(2S)-2-(15N)Azanylbutanedioic acid;L-ASPARATIC ACID-15N;CKLJMWTZIZZHCS-KPHKZEKTSA-N;HY-N0666S3;MFCD00055777;BS-46919;L-Aspartic acid-15N, 98 atom % 15N;CS-0356833;98 atom%;Chemical purity: inverted exclamation markY 98.5%

Chemical Property of L-Aspartic acid-15N

Chemical Property:

• Appearance/Colour: Colorless flaky crystal or white powder
• Melting Point: >300 °C (dec.)(lit.)
• PSA: 100.62000
• LogP: -0.42670
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: -2.8
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 134.03454260
• Heavy Atom Count: 9
• Complexity: 133

Purity/Quality:

98%,99%, ^*data from raw suppliers

L-Aspartic Acid-15N ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26-36

MSDS Files:

Useful:

• Canonical SMILES: C(C(C(=O)O)N)C(=O)O
• Isomeric SMILES: C([C@@H](C(=O)O)[15NH2])C(=O)O
• Uses: L-Aspartic Acid-15N is labelled L-Aspartic Acid (A790024), a non-essential amino acid found in food sources. L-Aspartic Acid is one of the 20 proteinogenic amino acids; the building blocks of proteins. Its conjugate base L-aspartate is an excitatory neurotransmitter in the central nervous system.

Technology Process of L-Aspartic acid-15N

There total 1 articles about L-Aspartic acid-15N 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: 62.0%

(2E)-but-2-enedioic acid (110-17-8,26099-09-2) → 15N-L-aspartic acid (3715-16-0)

Guidance literature:

With sodium azide; [¹⁵N]-ammonium hydroxide; immibilized aspartase; magnesium sulfate; for 216h;

DOI:10.1002/jccs.199800078

upstream raw materials:

(2E)-but-2-enedioic acid

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