102568-43-4

Sulfo-SANPAH Chemical Structure
102568-43-4

Chemical Structure

Sulfo-SANPAH

  • CAS No.: 102568-43-4
  • Formula:C16H18N6O9S
  • Molecular Weight:470.41

IUPAC Name: 1-((6-((4-azido-2-nitrophenyl)amino)hexanoyl)oxy)-2,5-dioxopyrrolidine-3-sulfonic acid

InChIKey: UPNUQQDXHCUWSG-UHFFFAOYSA-N

SMILES: O=C(ON1C(C(S(=O)(O)=O)CC1=O)=O)CCCCCNC2=CC=C(N=[N+]=[N-])C=C2[N+]([O-])=O

Biological Activity: Sulfo-SANPAH is a primary amine-nitrobenzene azide cross-linker. Sulfo-SANPAH improves the functionalization process of PDMS surfaces, is covalently bound to the PAAm gel surface. Sulfo-SANPAH is widely used to crosslink ECM proteins to various substrates, including acrylic-based hydrogels, such as polyacrylamide hydrogels. Sulfo-SANPAH facilitates covalent binding through its negatively charged sulfonate group on its N-hydroxysuccinimide ester ring and a photoactivated phenyl azide group that is highly reactive with nucleophiles and free radicals[1][2].

Cat. No. Product Name Purity Description Pricing
HY-137383
Sulfo-SANPAH 99.75% Sulfo-SANPAH is a primary amine-nitrobenzene azide cross-linker. Sulfo-SANPAH improves the functionalization process of PDMS surfaces, is covalently bound to the PAAm gel surface. Sulfo-SANPAH is widely used to crosslink ECM proteins to various substrates, including acrylic-based hydrogels, such as polyacrylamide hydrogels. Sulfo-SANPAH facilitates covalent binding through its negatively charged sulfonate group on its N-hydroxysuccinimide ester ring and a photoactivated phenyl azide group that is highly reactive with nucleophiles and free radicals.
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