Determine the necessary mass, volume, or concentration for preparing a solution.
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Moligand™,mol wt 500-5,000 Moligand™ 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 23 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Polyglycine has been used as an external intensity standard for measuring cross polarization (CP) nuclear magnetic resonance (NMR) spectrum measurements and ion mobility mass spectrometry. It is suitable for use as a model for UV resonance Raman spectroscopy studies.
| Sorrisi canonici | C(C(=O)O)N |
|---|---|
| IUPAC Name | 2-aminoacetic acid |
| InChIKey | DHMQDGOQFOQNFH-UHFFFAOYSA-N |
| INCHI | 1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5) |
| Isomeri SMILES | C(C(=O)O)N |
| CAS alternativo | 18875-39-3,56-40-6,25718-94-9,7490-95-1 (hydrochloride (2:1)) |
| Numero NSC | 25936 |
| Termini MeSH | Acid, Aminoacetic;Aminoacetic Acid;Calcium Salt Glycine;Cobalt Salt Glycine;Copper Salt Glycine;Glycine;Glycine Carbonate (1:1), Monosodium Salt;Glycine Carbonate (2:1), Monolithium Salt;Glycine Carbonate (2:1), Monopotassium Salt;Glycine Carbonate (2:1), |
| Reaxy-Rn | 635782 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635782&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 |
| Classe | 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 Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound |
| Descrizione | 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 | Common amino acids - Amino acids |
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| Punto di infiammabilità (°F) | Not applicable |
|---|---|
| Punto di infiammabilità (°C) | Not applicable |
| Punto di fusione (°C) | 300℃ |
| Peso molecolare | 75.070 g/mol |
| XLogP3 | -3.200 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 75.032 Da |
| Monoisotopic Mass | 75.032 Da |
| Topological Polar Surface Area | 63.300 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 42.900 |
| 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 |
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