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Photoactive, heterobifunctional cross-linking reagent incorporating an extended spacer. Ordinarily, initial reaction couples via ester to primary amine by amide bond formation in the pH range of 6.5-8.5. Second bonding occurs during UV irradiation (250-350 nm) via reactive nitrene. The latter bonding is non-specific and rapid. Note that the nitro substituent provides an absorption band at a longer wavelength compared to simple aryl azide.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
6-(4-Azido-2-nitrophenylamino)hexanoic acid N-hydroxysuccinimide ester, 50 mg | sc-256960 | 50 mg | $516.00 |