(5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic Acid

CAS: 113231-05-3

Ref. TR-A603250

Produktinformation

• Name: (5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic Acid
• Synonyme: (2S)-6-amino-2-[bis(carboxymethyl)amino]hexanoic acid;hydrate, (S)-2,2′-((5-Amino-1-carboxypentyl)azanediyl)diacetic acid, (S)-N-(5-Amino-1-Carboxypentyl)Iminodiacetic Acid, 13: PN: US20080160089 PAGE: 30 claimed protein, 1: PN: US20050123932 PAGE: 1 claimed protein, 4: PN: WO2004072260 PAGE: 12 claimed protein, 53: PN: WO2004025259 PAGE: 47 claimed protein, <span class="text-smallcaps">L</span>-Lysine, N²,N²-bis(carboxymethyl)-, Ab-Nta, Lysine-N,N-diacetic acid, N-(5-Amino-1-carboxypentyl)iminodiacetic acid, N-Alpha,N-Alpha-Bis(Carboxymethyl)-L-Lysine Hydrate, N2,N2-bis(carboxymethyl)-L-Lysine, N²,N²-Bis(carboxymethyl)-<span class="text-smallcaps">L</span>-lysine, N~2~,N~2~-bis(carboxymethyl)-D-lysine, Nα,Nα-Bis(Carboxymethyl)-L-Lysine Hydrate

Beschreibung

Applications A nitrilotriacetic acid derivative used as a metal chelating adsorbent for metal ion affinity chromatography. This method can be used for identification and rapid one-step purification of gene products expressed as fusion proteins with an oligo-histidine tag. The oligo-histidine tag serves as a high affinity binding sequence for the purification of fusion proteins via a metal chelating absorbent such as N-(5-Amino-1-carboxypentyl)iminodiacetic acid.Also soluble in DMSO:DMF 1:1 and DMSO:CH2Cl2 1:2
References Hochuli, E., et al.: J. Chromatography, 411, 177 (1987), Meredith, G.D., et al.: Bioconjugate Chem., 15, 969 (2004)

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 280.28
• Formel: C₁₀H₁₈N₂O₆·H₂O
• Farbe/Form: Neat
• InChl: InChI=1S/C10H18N2O6.H2O/c11-4-2-1-3-7(10(17)18)12(5-8(13)14)6-9(15)16;/h7H,1-6,11H2,(H,13,14)(H,15,16)(H,17,18);1H2/t7-;/m0./s1
• InChI Key: InChIKey=SYFQYGMJENQVQT-ZETCQYMHSA-N
• SMILES: NCCCC[C@@H](C(=O)O)N(CC(=O)O)CC(=O)O