≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504758677 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758677 |
| Sonrisas canónicas | C(CNCC(=O)O)N |
| IUPAC Name | 2-(2-aminoethylamino)acetic acid |
| InChIKey | PIINGYXNCHTJTF-UHFFFAOYSA-N |
| INCHI | 1S/C4H10N2O2/c5-1-2-6-3-4(7)8/h6H,1-3,5H2,(H,7,8) |
| Isómeros SMILES | C(CNCC(=O)O)N |
| Peso molecular | 118.14 |
| Reaxy-Rn | 1748916 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1748916&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 |
| Clase | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Alpha amino acids |
| Alternative Parents | Amino acids Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-amino acid - Amino acid - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Carbonyl group - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organopnictogen compound - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). |
| External Descriptors | Not available |
| Solubilidad | Soluble in Methanol and Water |
|---|---|
| Punto de fusión (°C) | 143°C |
| Peso molecular | 118.130 g/mol |
| XLogP3 | -3.800 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 118.074 Da |
| Monoisotopic Mass | 118.074 Da |
| Topological Polar Surface Area | 75.400 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 74.400 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 |
| 1. Daoyuan Zu, Haoran Song, Changping Li, Yuwei Wang, Rong Du, Rui Zhou, Wei Zhang, Shiting Pan, Yang Cai, Yongming Shen, Zhifeng Yang. (2022) Understanding the self-catalyzed decomplexation mechanism of Cu-EDTA in Ti3C2Tx MXene/peroxymonosulfate process. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2022.121131] |
| 2. Jinhua Xu, Jinyu Zhang, Wenmin Zhang, Shiye Xie, Lan Zhang. (2025) Controllable synthesis of chiral hierarchical porous Co(OH)2 and its application in rapid chiral recognition and separation. ANALYTICA CHIMICA ACTA, [PMID:40480689] [10.1016/j.aca.2025.344212] |
K2316022