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5-AZIDO-2-NITROBENZOIC ACID N-HYDROXY&
Кат. №: A3282-100MG
CAS: 60117-35-3
Производитель: Sigma-Aldrich
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Цена по запросу
Товар оформляется под заказ
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5-AZIDO-2-NITROBENZOIC ACID N-HYDROXY&
Main image
Кат. №: A3282-100MG
CAS: 60117-35-3
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
5-AZIDO-2-NITROBENZOIC ACID N-HYDROXY&
Кат. №: A3282-100MG
CAS: 60117-35-3
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Packaging 100 mg in poly bottle Application Photoactive, heterobifunctional cross-linking reagent. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. Second bonding occurs during UV irradiation (250-350 nm) via reactive nitrene. The latter bonding is rapid and non-specific. Caution Reducing agents such as thiols may reduce the azide to amine and should be avoided. Initial manipulations and coupling should be performed under reduced light. Other Notes Note that the nitro substituent provides an absorption band at a longer wavelength compared to simple aryl azide.
Related Categories
Chemical Biology, Chemical Synthesis, Crosslinkers, Crosslinking, Heterobifunctional Cross-Linking Reagents, Linkers and Crosslinkers, Molecular Biology, Photoactive, Protein Modification, Protein Structural Analysis, Proteomics More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Packaging 100 mg in poly bottle Application Photoactive, heterobifunctional cross-linking reagent. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. Second bonding occurs during UV irradiation (250-350 nm) via reactive nitrene. The latter bonding is rapid and non-specific. Caution Reducing agents such as thiols may reduce the azide to amine and should be avoided. Initial manipulations and coupling should be performed under reduced light. Other Notes Note that the nitro substituent provides an absorption band at a longer wavelength compared to simple aryl azide.
Related Categories
Chemical Biology, Chemical Synthesis, Crosslinkers, Crosslinking, Heterobifunctional Cross-Linking Reagents, Linkers and Crosslinkers, Molecular Biology, Photoactive, Protein Modification, Protein Structural Analysis, Proteomics More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.