Sulfo-N-succinimidyl (N-Iodoacetyl)aminobenzoate

Reagent Code: #237984
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CAS Number 144650-93-1

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scatter_plot Molecular Information
Weight 504.19 g/mol
Formula C₁₃H₁₀IN₂NaO₈S
badge Registry Numbers
MDL Number MFCD00054977
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in bioconjugation for crosslinking proteins and labeling biomolecules. It reacts selectively with thiol groups (cysteine residues) in proteins to form stable thioether bonds, making it ideal for preparing protein-protein conjugates or attaching fluorescent dyes, biotin, or other probes. Commonly used in preparing immunoassays, enzyme labeling, and immobilizing biomolecules on surfaces. Its iodoacetyl group ensures high reactivity and specificity toward sulfhydryls, while the sulfo-NHS ester enables water solubility and efficient coupling to primary amines under mild conditions. Suitable for applications requiring controlled, site-specific modifications in aqueous buffers at near-neutral pH.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,350.00
inventory 100mg
10-20 days ฿46,040.00
Sulfo-N-succinimidyl (N-Iodoacetyl)aminobenzoate
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Used in bioconjugation for crosslinking proteins and labeling biomolecules. It reacts selectively with thiol groups (cysteine residues) in proteins to form stable thioether bonds, making it ideal for preparing protein-protein conjugates or attaching fluorescent dyes, biotin, or other probes. Commonly used in preparing immunoassays, enzyme labeling, and immobilizing biomolecules on surfaces. Its iodoacetyl group ensures high reactivity and specificity toward sulfhydryls, while the sulfo-NHS ester enables

Used in bioconjugation for crosslinking proteins and labeling biomolecules. It reacts selectively with thiol groups (cysteine residues) in proteins to form stable thioether bonds, making it ideal for preparing protein-protein conjugates or attaching fluorescent dyes, biotin, or other probes. Commonly used in preparing immunoassays, enzyme labeling, and immobilizing biomolecules on surfaces. Its iodoacetyl group ensures high reactivity and specificity toward sulfhydryls, while the sulfo-NHS ester enables water solubility and efficient coupling to primary amines under mild conditions. Suitable for applications requiring controlled, site-specific modifications in aqueous buffers at near-neutral pH.

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