Basic information Safety Supplier Related

P-BROMOACETAMIDO BENZYL-EDTA

Basic information Safety Supplier Related

P-BROMOACETAMIDO BENZYL-EDTA Basic information

Product Name:
P-BROMOACETAMIDO BENZYL-EDTA
Synonyms:
  • P-BROMOACETAMIDO BENZYL-EDTA
  • 1-(p-Bromoacetamidobenzyl)-ethylenediamineN,N,N',N'-tetraaceticacid
  • 1-(4-bromoacetamidobenzyl)EDTA
  • (S)-1-(4-bromoacetamidobenzyl)EDTA
  • (S)-1-(p-Bromoacetamidobenzyl)ethylenediaminetetraacetic Acid (~80%)
  • N,N'-[(1S)-1-[[4-[(BroMoacetyl)aMino]phenyl]Methyl]-1,2-ethanediyl]bis[N-(carboxyMethyl)-glycine
  • Glycine, N,N'-[(1S)-1-[[4-[(2-bromoacetyl)amino]phenyl]methyl]-1,2-ethanediyl]bis[N-(carboxymethyl)-
  • EDTA-p-Bromoacetamido benzyl
CAS:
81677-64-7
MF:
C19H24BrN3O9
MW:
518.31
Product Categories:
  • Chelating Agents & Ligands
  • MTS & Sulfhydryl Active Reagents
  • Chelating Agents, Ligands
Mol File:
81677-64-7.mol
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P-BROMOACETAMIDO BENZYL-EDTA Chemical Properties

Melting point:
112-114°C
storage temp. 
Hygroscopic, -20°C Freezer, Under Inert Atmosphere
solubility 
Methanol (Slightly, Heated), Water (Slightly, Heated, Sonicated)
form 
Solid
color 
White to Light Yellow
Stability:
Hygroscopic
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P-BROMOACETAMIDO BENZYL-EDTA Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

A bifunctional iron chelating agent that has been employed to couple metal ions to biological molecules, including radiopharmaceutical synthesis and targeted protein hydrolysis. Bifunctional chelating reagents possess both a strong metal-binding moiety and a group that binds to a biological molecule.

Definition

ChEBI: A tetracarboxylic acid consisting of ethylenediaminetetraacetic acid having a 4-bromoacetamidobenzyl group at the C1-position and (S)-configuration.

P-BROMOACETAMIDO BENZYL-EDTASupplier

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