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ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Lysine derivatives >  (S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE

(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE

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(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE Basic information

Product Name:
(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE
Synonyms:
  • (S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE
  • N-ALPHA,N-ALPHA-BIS(CARBOXYMETHYL)-L-LYSINE HYDRATE
  • AB-NTA
  • N2,N2-Bis(carboxyMethyl)-L-lysine
  • (S)-2,2'-((5-AMino-1-carboxypentyl)azanediyl)diacetic acid
  • N-(5-Amino-1-carboxypentyl)iminodiacetic disodium salt monohydrate
  • Nα, Nα-Bis(carboxymethyl)-L-lysine disodium salt monohydrate
  • L-Lysine,N2,N2-bis(carboxymethyl)-
CAS:
113231-05-3
MF:
C10H18N2O6
MW:
262.26
Product Categories:
  • Amino Acids & Derivatives
  • Chelating Agents & Ligands
Mol File:
113231-05-3.mol
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(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE Chemical Properties

Melting point:
>208°C
Boiling point:
537.8±50.0 °C(Predicted)
Density 
1.389
storage temp. 
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility 
Aqueous Acid (Slightly), Methanol (Very Slightly, Heated), Water (Sparingly)
form 
Solid
pka
1.67±0.10(Predicted)
color 
White to Off-White
Stability:
Moisture Sensitive
InChIKey
SYFQYGMJENQVQT-ZETCQYMHSA-N
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Safety Information

WGK Germany 
3
HS Code 
2922498590

MSDS

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(S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE Usage And Synthesis

Chemical Properties

(5S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE is Off-White Solid

Uses

(5S)-N-(5-AMINO-1-CARBOXYPENTYL)IMINODIACETIC ACID HYDRATE 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 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

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