Nitrilotriacetic Acid

CAS: 139-13-9

Ref. TR-N490175

Produktinformation

• Name: Nitrilotriacetic Acid
• Synonyme: 2-[Bis(carboxymethyl)amino]acetic acid, NTA, (Bis-carboxymethyl-amino)-acetic acid, 412: PN: WO2007070372 PAGE: 72 claimed protein, Acetic acid, nitrilotri-, Acide nitrilotriacetique, Acido Nitrilotriacetico, Ai3-52483, Alpha,Alpha',Alpha''-Trimethylaminetricarboxylic Acid, Aminotriacetic Acid, Chel 300, Chel300, Chelest NT, Complexon I, Complexoni, Dissolvine A, Dissolvine AZ, Glycine, N,N-bis(carboxymethyl)-, Glycine,N,N-bis(carboxyme, Glycine-N,N-diacetic acid, Hampshire Nta Acid, Hampshirentaacid, Komplexoni, Kyselinanitrilotrioctova, Kyselinanitrilotrioctova(Czech), N 0098, N,N-bis(carboxymethyl)glycine, NTA N,N-Bis(carboxymethyl)glycine, Nitrilo triacetic acid, Nitrilo-2,2',2''-Triacetic Acid, Nitrilo-2,2′,2′′-triacetic acid, Nitrilo-N,N,N-triacetic acid, Nitrilotriessigsaeure, Nitrilotriessigsaure, Nitrilotris(methylenecarboxylic acid), Nsc 2121, Titriplex I, Tri(Carboxymethyl)Amine, Tricollamic acid, Triglycine, Triglycollamic Acid, Trilon AS, Trilone A, Trimethylamine-α,α',α"-tricarboxylic acid, Tris(carboxymethyl)amine, Tris(hydroxycarbonylmethyl)amine, Versene Nta Acid, α,α',α''-Trimethylaminetricarboxylic acid
• CAS: 139-13-9

Beschreibung

Applications Nitrilotriacetic acid is a chelating agent which forms coordination compounds with metal ions. Nitrilotriacetic acid is used in complexometric titrations and as well as for protein isolation and purification in the His-tag method. This compound is a contaminant of emerging concern (CECs).
References Smolinska, B., et al: J. Chem. Tech. Biotech., 87, 1360 (2012); Kaluza, L., et al.: Catalysis. Letters., 142, 969 (2012); Tragardh, G., et al.: Desalination., 119, 21 (1998);

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 191.14
• Formel: C₆H₉NO₆
• Farbe/Form: White To Off-White
• InChl: InChI=1S/C6H9NO6/c8-4(9)1-7(2-5(10)11)3-6(12)13/h1-3H2,(H,8,9)(H,10,11)(H,12,13)
• InChI Key: InChIKey=MGFYIUFZLHCRTH-UHFFFAOYSA-N
• SMILES: O=C(O)CN(CC(=O)O)CC(=O)O