25713-23-9

Basic information

• Product Name: H-[15N]ALA-OH
• Synonyms: [15N]-L-ALANINE;[15N]ALANINE;L-ALANINE-15N;H-[15N]ALA-OH;D-ALANINE 15N, 98 ATOM % 15N;L-ALANINE-15N, 98 ATOM % 15N;L-[15N]Alanine;(S)-2-Aminopropionic acid-15N
• CAS NO: 25713-23-9
• Molecular Formula: C₃H₇NO₂
• Molecular Weight: 90.1
• Product Categories: Amino Acids 13C, 2H, 15N;Alphabetical Listings;Amino Acids;Amino Acids and DerivativesMass Spectrometry;Amino AcidsStable Isotopes;AStable Isotopes;Biomolecular MS;Biomolecular NMR;Labeled Amino AcidsStable Isotopes;Products for SILAC;Proteomics Stable Isotope Labeling;Stable Isotopes
• Mol File: 25713-23-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 314.5 °C (dec.)(lit.)
• Appearance: /
• Storage Temp.: -15°C
• CAS DataBase Reference: H-[15N]ALA-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-[15N]ALA-OH(25713-23-9)
• EPA Substance Registry System: H-[15N]ALA-OH(25713-23-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 25713-23-9(Hazardous Substances Data)

Usage

Chemical Properties

Solid

Upstream product

• 113-24-6 sodium pyruvate 
• 598-72-1 2-Bromopropionic acid 
• 201230-82-2 carbon monoxide 

Relevant articles and documents

Synthesis of α-amino and α-hydroxy acids under volcanic conditions: implications for the origin of life

Facile synthesis of α-hydroxy and α-amino acids is observed at temperatures from 145 to 280 °C with catalytic Ni2+, with cyano ligands as source for C and N, and with CO as a reductant and as a source for C. Implications for the problem of the origin of life are discussed.

Stereoselective synthesis of stable isotope-labeled L-α-amino acids: Electrophilic amination of oppolzer's acyl sultams in the synthesis of L-[15N]alanine, L-[15N]valine, L-[15N]leucine, L-[15N]phenylalanine and

Using 1-chloro-1-[15N]nitrosocyclohexane, we have prepared five L-[α-15N]amino acids. The stereoselective electophillic hydroxyamination of (S)-acylbornane-10,2-sultams, followed by Zn(o)/H+ reduction, and alkaline cleavag