N-Succinimidyl 3-Methoxy-4-nitrobenzoate

97%

Reagent Code: #220243
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CAS Number 2006277-78-5

science Other reagents with same CAS 2006277-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.22 g/mol
Formula C₁₂H₁₀N₂O₇
badge Registry Numbers
MDL Number MFCD29065913
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in bioconjugation processes to modify proteins and peptides by introducing a stable ester linkage. It reacts selectively with primary amines, such as those found on lysine residues, enabling the attachment of labels, tags, or functional groups. Commonly applied in the development of immunoassays, antibody-drug conjugates, and diagnostic probes due to its ability to enhance coupling efficiency under mild reaction conditions. The methoxy and nitro groups contribute to increased solubility and reaction kinetics in aqueous-organic mixtures. Stable at room temperature when dry, it allows for convenient handling in labeling workflows.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,980.00
inventory 1g
10-20 days ฿12,600.00
inventory 5g
10-20 days ฿38,700.00
inventory 10g
10-20 days ฿59,000.00
inventory 25g
10-20 days ฿129,800.00
N-Succinimidyl 3-Methoxy-4-nitrobenzoate
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Used in bioconjugation processes to modify proteins and peptides by introducing a stable ester linkage. It reacts selectively with primary amines, such as those found on lysine residues, enabling the attachment of labels, tags, or functional groups. Commonly applied in the development of immunoassays, antibody-drug conjugates, and diagnostic probes due to its ability to enhance coupling efficiency under mild reaction conditions. The methoxy and nitro groups contribute to increased solubility and reaction

Used in bioconjugation processes to modify proteins and peptides by introducing a stable ester linkage. It reacts selectively with primary amines, such as those found on lysine residues, enabling the attachment of labels, tags, or functional groups. Commonly applied in the development of immunoassays, antibody-drug conjugates, and diagnostic probes due to its ability to enhance coupling efficiency under mild reaction conditions. The methoxy and nitro groups contribute to increased solubility and reaction kinetics in aqueous-organic mixtures. Stable at room temperature when dry, it allows for convenient handling in labeling workflows.

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