CAS 113231-05-3
:(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE
Description:
(S)-N-(5-Amino-1-carboxypentyl)iminodiacetic acid hydrate, commonly referred to as a chelating agent, is characterized by its ability to form stable complexes with metal ions, which is particularly useful in various biochemical applications. This compound features a chiral center, indicating that it exists in two enantiomeric forms, with the (S)-configuration being biologically relevant. The presence of amino and carboxyl functional groups contributes to its solubility in water and its potential as a ligand in coordination chemistry. The imino group enhances its chelating properties, allowing it to effectively bind to divalent and trivalent metal ions, which is valuable in fields such as medicine, agriculture, and environmental science. Additionally, the hydrate form indicates that it contains water molecules, which can influence its stability and reactivity. Overall, this compound is significant in research and industrial applications where metal ion sequestration is required.
Formula:C10H18N2O6
InChI:InChI=1S/C10H18N2O6/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)/t7-/m0/s1
InChI key:InChIKey=SYFQYGMJENQVQT-ZETCQYMHSA-N
SMILES:N([C@@H](CCCCN)C(O)=O)(CC(O)=O)CC(O)=O
Synonyms:- (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, N<sup>2</sup>,N<sup>2</sup>-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
- N<sup>2</sup>,N<sup>2</sup>-Bis(carboxymethyl)-<span class="text-smallcaps">L</span>-lysine
- N~2~,N~2~-bis(carboxymethyl)-D-lysine
- Nα,Nα-Bis(Carboxymethyl)-L-Lysine Hydrate
- See more synonyms
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Found 8 products.
N2,N2-Bis(carboxymethyl)-L-lysine
CAS:Formula:C10H18N2O6Purity:>95.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:262.26(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE
CAS:Formula:C10H18N2O6Purity:97%Color and Shape:SolidMolecular weight:262.2597(5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic acid
CAS:(5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic acidPurity:97%Color and Shape:White To Off White SolidMolecular weight:262.26g/mol(5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic acid
CAS:Purity:≥ 97.0%Color and Shape:White to off-white crystalline powderMolecular weight:262.26Lysine-N,N-diacetic acid
CAS:<p>Lysine-N,N-diacetic acid (BCML) is a highly efficient TAS2R4 inhibitor, blocking the human TAS2R4-mediated response to quinine.</p>Formula:C10H18N2O6Purity:99.76%Color and Shape:SolidMolecular weight:262.26(5S)-N-(5-Amino-1-carboxypentyl)iminodiacetic Acid
CAS:Controlled Product<p>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<br>References Hochuli, E., et al.: J. Chromatography, 411, 177 (1987), Meredith, G.D., et al.: Bioconjugate Chem., 15, 969 (2004)<br></p>Formula:C10H18N2O6·H2OColor and Shape:NeatMolecular weight:280.28Nα,Nα-Bis-(carboxymethyl)-L-lysine
CAS:<p>Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine is a synthetic amino acid that has been used to immobilize proteins and enzymes. It can be used as an inhibitor in cell culture because it binds to the ryanodine receptor, which regulates calcium release from the sarcoplasmic reticulum. This amino acid has also been shown to inhibit kinesin, a protein involved in the movement of organelles along microtubules. In addition, Nalpha,Nalpha-Bis-(carboxymethyl)-L-lysine has been found to be effective against colony-stimulating factor (CSF) and may serve as a model system for enzymatic reactions.</p>Formula:C10H18N2O6Purity:Area-% Max. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:262.26 g/mol(S)-2,2′-((5-Amino-1-carboxypentyl)azanediyl)diacetic acid
CAS:Formula:C10H18N2O6Purity:95%Color and Shape:SolidMolecular weight:262.262








