N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER
N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER Basic information
- Product Name:
- N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER
- Synonyms:
-
- N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER
- N2,N2-Bis[2-(1,1-diMethylethoxy)-2-oxoethyl]-L-lysine 1,1-DiMethylethyl Ester
- L-Lysine, N2,N2-bis[2-(1,1-diMethylethoxy)-2-oxoethyl]-, 1,1-diMethylethyl ester
- Nα,Nα-bis[(tert-butyloxycarbonyl)methyl]-L-lysine tert-butyl ester
- CAS:
- 205379-08-4
- MF:
- C22H42N2O6
- MW:
- 430.58
- Product Categories:
-
- Amino Acids & Derivatives
- Chelating Agents & Ligands
- Chelating Agents, Ligands
- Mol File:
- Mol File
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N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER Chemical Properties
- storage temp.
- -20°C Freezer
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Oil
- color
- Yellow
- Stability:
- Moisture Sensitive
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N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID, TRI-T-BUTYL ESTER Usage And Synthesis
Chemical Properties
Yellow Oil
Uses
N-(5-AMino-1-carboxypentyl)iMinodiacetic Acid Tri-t-butyl Ester is 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 produc ts 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.
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