N-Succinimidyl Maleimidoacetate

98%

Reagent Code: #217436
label
Alias N-(A-maleimide acetic acid)N-succinate imidyl ester; N-succinimide acetic acid N-succinimide acetic acid; active maleimide acetic acid
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CAS Number 55750-61-3

science Other reagents with same CAS 55750-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.18 g/mol
Formula C₁₀H₈N₂O₆
badge Registry Numbers
MDL Number MFCD00133523
thermostat Physical Properties
Melting Point 174-175 °C
Boiling Point 430.1±47.0 °C
inventory_2 Storage & Handling
Density 1.63±0.1 g/cm3
Storage -20°C, Inert Gas Storage

description Product Description

Used in bioconjugation to link proteins, peptides, or other biomolecules to surfaces or labels. Its maleimide group reacts selectively with thiol groups (-SH) on cysteine residues, while the NHS ester end binds to primary amines (-NH₂) on molecules like antibodies or fluorescent tags. Commonly used in preparing antibody-drug conjugates, immobilizing enzymes on biosensor surfaces, and labeling proteins for imaging or detection. Stable in aqueous solution for short periods, allowing efficient coupling under mild conditions. Preferred in creating targeted therapeutics and diagnostic probes due to its specific, controlled reactivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿770.00
250mg
10-20 days ฿1,330.00
1g
10-20 days ฿4,080.00
5g
10-20 days ฿15,520.00
25g
10-20 days ฿59,880.00
N-Succinimidyl Maleimidoacetate
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Used in bioconjugation to link proteins, peptides, or other biomolecules to surfaces or labels. Its maleimide group reacts selectively with thiol groups (-SH) on cysteine residues, while the NHS ester end binds to primary amines (-NH₂) on molecules like antibodies or fluorescent tags. Commonly used in preparing antibody-drug conjugates, immobilizing enzymes on biosensor surfaces, and labeling proteins for imaging or detection. Stable in aqueous solution for short periods, allowing efficient coupling unde

Used in bioconjugation to link proteins, peptides, or other biomolecules to surfaces or labels. Its maleimide group reacts selectively with thiol groups (-SH) on cysteine residues, while the NHS ester end binds to primary amines (-NH₂) on molecules like antibodies or fluorescent tags. Commonly used in preparing antibody-drug conjugates, immobilizing enzymes on biosensor surfaces, and labeling proteins for imaging or detection. Stable in aqueous solution for short periods, allowing efficient coupling under mild conditions. Preferred in creating targeted therapeutics and diagnostic probes due to its specific, controlled reactivity.

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