Mal-amido-(CH2COOH)2

99%

Reagent Code: #203972
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CAS Number 207613-14-7

science Other reagents with same CAS 207613-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.22 g/mol
Formula C₁₁H₁₂N₂O₇
badge Registry Numbers
MDL Number MFCD34469576
thermostat Physical Properties
Boiling Point 620.2±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.580±0.06 g/cm3(Predicted)
Storage -20°C

description Product Description

Used as a bifunctional crosslinking agent in bioconjugation, particularly for attaching fluorescent dyes, drugs, or other functional molecules to proteins, peptides, or nanoparticles. The maleimide group selectively reacts with thiol groups (-SH) under mild conditions, forming stable thioether bonds, while the two carboxylic acid groups allow further activation and coupling to amine-containing molecules via EDC/NHS chemistry. Commonly employed in the development of antibody-drug conjugates (ADCs), targeted therapies, and diagnostic probes. Its hydrophilic nature helps improve solubility and reduce aggregation in aqueous biological systems.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿30,950.00

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Mal-amido-(CH2COOH)2
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Used as a bifunctional crosslinking agent in bioconjugation, particularly for attaching fluorescent dyes, drugs, or other functional molecules to proteins, peptides, or nanoparticles. The maleimide group selectively reacts with thiol groups (-SH) under mild conditions, forming stable thioether bonds, while the two carboxylic acid groups allow further activation and coupling to amine-containing molecules via EDC/NHS chemistry. Commonly employed in the development of antibody-drug conjugates (ADCs), target

Used as a bifunctional crosslinking agent in bioconjugation, particularly for attaching fluorescent dyes, drugs, or other functional molecules to proteins, peptides, or nanoparticles. The maleimide group selectively reacts with thiol groups (-SH) under mild conditions, forming stable thioether bonds, while the two carboxylic acid groups allow further activation and coupling to amine-containing molecules via EDC/NHS chemistry. Commonly employed in the development of antibody-drug conjugates (ADCs), targeted therapies, and diagnostic probes. Its hydrophilic nature helps improve solubility and reduce aggregation in aqueous biological systems.

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