3-(2-Pyridyldithio)propionic Acid N-Succinimidyl Ester

≥95%

Reagent Code: #225263
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CAS Number 68181-17-9

science Other reagents with same CAS 68181-17-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.36 g/mol
Formula C₁₂H₁₂N₂O₄S₂
badge Registry Numbers
MDL Number MFCD00009636
thermostat Physical Properties
Melting Point 84-86°C (Lit.)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in bioconjugation processes to link proteins, antibodies, or peptides with other molecules such as drugs, labels, or nanoparticles. Its primary application is in the development of antibody-drug conjugates (ADCs), where it enables controlled attachment through disulfide bond formation. The N-hydroxysuccinimide ester group reacts efficiently with primary amines on biomolecules, while the pyridyldithio group allows for thiol-disulfide exchange, facilitating reversible linkage. This makes it valuable in targeted drug delivery systems and diagnostic probes. Also employed in immobilizing biomolecules onto surfaces for biosensors or assay platforms due to its stable yet cleavable linker properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿300.00
inventory 100mg
10-20 days ฿580.00
inventory 1g
10-20 days ฿2,800.00
inventory 5g
10-20 days ฿8,980.00
inventory 25g
10-20 days ฿42,890.00
3-(2-Pyridyldithio)propionic Acid N-Succinimidyl Ester
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Used in bioconjugation processes to link proteins, antibodies, or peptides with other molecules such as drugs, labels, or nanoparticles. Its primary application is in the development of antibody-drug conjugates (ADCs), where it enables controlled attachment through disulfide bond formation. The N-hydroxysuccinimide ester group reacts efficiently with primary amines on biomolecules, while the pyridyldithio group allows for thiol-disulfide exchange, facilitating reversible linkage. This makes it valuable i

Used in bioconjugation processes to link proteins, antibodies, or peptides with other molecules such as drugs, labels, or nanoparticles. Its primary application is in the development of antibody-drug conjugates (ADCs), where it enables controlled attachment through disulfide bond formation. The N-hydroxysuccinimide ester group reacts efficiently with primary amines on biomolecules, while the pyridyldithio group allows for thiol-disulfide exchange, facilitating reversible linkage. This makes it valuable in targeted drug delivery systems and diagnostic probes. Also employed in immobilizing biomolecules onto surfaces for biosensors or assay platforms due to its stable yet cleavable linker properties.

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