L-ASPARTIC ACID-13C4, 15N, 99 ATOM % 13C

Base Information

• Chemical Name: L-ASPARTIC ACID-13C4, 15N, 99 ATOM % 13C
• CAS No.: 55443-54-4
• Molecular Formula: C4H7NO4
• Molecular Weight: 133.10268
• Mol file: 55443-54-4.mol

Synonyms:L-ASPARTIC ACID-13C4, 15N, 99 ATOM % 13C

Chemical Property of L-ASPARTIC ACID-13C4, 15N, 99 ATOM % 13C

Chemical Property:

• Melting Point: >300°C (dec.) (lit.)
• PSA: 100.62000
• LogP: -0.42670
• Storage Temp.: Hygroscopic, -20°C Freezer, Under inert atmosphere
• Solubility.: Aqueous Acid (Very Slightly), Aqueous Base (Slightly)

Purity/Quality:

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

L-Aspartic-13C4Acid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: L-Aspartic Acid (13C4, 99%) Microbiological/Pyrogen Tested. Labelled analogue of L-Aspartic Acid, a non-essential amino acid found in food sources. 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-13C4, 15N, 99 ATOM % 13C

There total 2 articles about L-ASPARTIC ACID-13C4, 15N, 99 ATOM % 13C 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:

[13C]methanol (14742-26-8) → U-(13)C-L-aspartic acid (55443-54-4,81201-98-1,68315-35-5) + 1,2-13C2-glycine (67836-01-5) + (13)C3H8N2O2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H7NO4 (1202063-43-1,55443-54-4,81201-98-1,68315-35-5) + (13)C5H7NO3 (55443-56-6) + (13)C5H7NO3 + (13)C4H10N2O2 + (13)C4H10N2O2 + (13)C4H10N2O2 (1391068-14-6) + (13)C4H10N2O2 + (13)C4H8N2O3 + (13)C5H9NO2 (81202-06-4) + (13)C5H11NO2 + (13)C3H7NO2 + (13)C5H11NO2 + (13)C5H9NO3 + (13)C5H11NO2 + (13)C4H9NO2 + (13)C3H7NO2 + (13)C3H8N2O2 + (13)C3H8N2O2 + (13)C3H8N2O2 + (13)C3H7NO2 (286460-72-8,65163-26-0,70753-82-1) + alanine 13C315N (100108-77-8,65163-26-0,70753-82-1)

Guidance literature:

[¹³C]methanol; With ammonia; water; at -193.16 ℃; for 240h; under 7.50075E-08 Torr; Microwave irradiation;

With hydrogenchloride; water; at 110 ℃; for 24h;

DOI:10.1002/cplu.201100048

Reference yield:

[13C]methanol (14742-26-8) → U-(13)C-L-aspartic acid (55443-54-4,81201-98-1,68315-35-5) + 1,2-13C2-glycine (67836-01-5) + (13)C3H8N2O2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H9NO2 + (13)C4H7NO4 (1202063-43-1,55443-54-4,81201-98-1,68315-35-5) + (13)C5H7NO3 (55443-56-6) + (13)C5H7NO3 + (13)C4H10N2O2 + (13)C4H10N2O2 + (13)C4H10N2O2 (1391068-14-6) + (13)C4H10N2O2 + (13)C4H8N2O3 + (13)C5H9NO2 (81202-06-4) + (13)C5H11NO2 + (13)C3H7NO2 + (13)C5H11NO2 + (13)C5H9NO3 + (13)C5H11NO2 + (13)C4H9NO2 + (13)C3H7NO2 + (13)C3H8N2O2 + (13)C3H8N2O2 + (13)C3H8N2O2 + (13)C3H7NO2 (286460-72-8,65163-26-0,70753-82-1) + alanine 13C315N (100108-77-8,65163-26-0,70753-82-1)

Guidance literature:

[¹³C]methanol; With ammonia; water; at -193.16 ℃; for 240h; under 7.50075E-08 Torr; Microwave irradiation;

With hydrogenchloride; water; at 110 ℃; for 24h;

DOI:10.1002/cplu.201100048

upstream raw materials:

[¹³C]methanol

Refernces