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| Product | Description | |
|---|---|---|
| 2-(4-Nitrophenyl)sulfanylacetate; tris(2-hydroxyethyl)azanium | Heterocyclic Organic Compound. Alternative Names: ((4-Nitrophenyl)thio)acetic acid 2,2,2-nitrilotris(ethanol) (1:1); 2-(4-nitrophenyl)sulfanylacetate; tris(2-hydroxyethyl)azanium; 2-hydroxy-N,N-bis(2-hydroxyethyl)ethanaminium [(4-nitrophenyl)sulfanyl]acetate; Acetic acid,((4-nitrophenyl)thio)-,compd. wit. CAS No. 102582-90-1. Molecular formula: C14H22N2O7S. Mole weight: 362.399 g/mol. Purity: 0.96. IUPACName: 2-(4-nitrophenyl)sulfanylacetate;tris(2-hydroxyethyl)azanium. Canonical SMILES: C1=CC (=CC=C1[N+] (=O)[O-])SCC (=O)[O-]. C (CO)[NH+] (CCO)CCO. Catalog: ACM102582901. |  |
| Iminodiacetic acid | Iminodiacetic acid, HN(CH2CO2H)2, often abbreviated to IDA, is a dicarboxylic acid amine (the nitrogen atom forms a secondary amino group, not an imino group as the name suggests). The iminodiacetate anion can act as a tridentate ligand to form a metal complex with two, fused, five membered chelate rings. The proton on the nitrogen atom can be replaced by a carbon atom of a polymer to create an ion-exchange resin, such as chelex 100.IDA forms stronger complexes than the bidentate ligand glycine and weaker complexes than the tetradentate ligand nitrilotriacetic acid. It can also act as a bidentate ligand through its two carboxylate groups. Several technetium-99m complexes are used in cholescintigraphy scans (also known as hepatobiliary iminodiacetic acid scans) to evaluate the health and function of the gallbladder.Iminodiacetic acid is an important intermediate in one of the two main industrial processes used to manufacture the herbicide glyphosate. It is also used in capillary electrophoresis for modulating peptide mobility. Group: Heterocyclic organic compound. Alternative Names: 2-(carboxymethylamino)acetic acid;Iminodiacetic acid;2,2-Azanediyldiacetic acid;Glycine, N-(carboxymethyl)-. CAS No. 142-73-4. Molecular formula: C4H7NO4. Mole weight: 133.1. Appearance: White crystal. Density: 1.436 g/cm³. ECNumber: 205-555-4. Catalog: ACM142734. | |
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