≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
L-Albizziin a glutamase inhibitor, a GlnRS (glutaminyl-tRNA synthetase) inhibitor as well as an intermediate in the synthesis of heterocycles. L-Albizziin is also a potential effector group in affinity chromatography.
| Pubchem Sid | 504756148 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504756148 |
| Canonical Smiles | C(C(C(=O)O)N)NC(=O)N |
| IUPAC Name | (2S)-2-amino-3-(carbamoylamino)propanoic acid |
| InChIKey | GZYFIMLSHBLMKF-REOHCLBHSA-N |
| INCHI | 1S/C4H9N3O3/c5-2(3(8)9)1-7-4(6)10/h2H,1,5H2,(H,8,9)(H3,6,7,10)/t2-/m0/s1 |
| Isomeric SMILES | C([C@@H](C(=O)O)N)NC(=O)N |
| Molecular Weight | 147.13 |
| Reaxy-Rn | 1724320 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1724320&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids |
| Direct Parent | L-alpha-amino acids |
| Alternative Parents | Isoureas Amino acids Monocarboxylic acids and derivatives Carboxylic acids Carboximidamides Organopnictogen compounds Organic oxides Monoalkylamines Imines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | L-alpha-amino acid - Isourea - Amino acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Amine - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Imine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. |
| External Descriptors | non-proteinogenic L-alpha-amino acid |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 J2514110 | Certificate of Analysis | Oct 17, 2025 | L344148 |
| K2218523 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| K2218524 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| K2218525 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| K2218543 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| K2218613 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| K2218614 | Certificate of Analysis | Sep 04, 2025 | L344148 |
| Solubility | Soluble in Water |
|---|---|
| Specific Rotation[α] | -65.8° (c = 0.2, Water) |
| Melt Point(°C) | 218-220°C (lit.)(dec.) |
| Molecular Weight | 147.130 g/mol |
| XLogP3 | -4.600 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 3 |
| Exact Mass | 147.064 Da |
| Monoisotopic Mass | 147.064 Da |
| Topological Polar Surface Area | 118.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 147.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
