N-Succinimidyl Iodoacetate

95%

Reagent Code: #218501
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Alias Succinimide iodoacetate; N-succinimide iodoacetate
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CAS Number 39028-27-8
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Properties Solubility DMF: 50 mg/mL

science Other reagents with same CAS 39028-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.02 g/mol
Formula C₆H₆INO₄
badge Registry Numbers
MDL Number MFCD00058451
thermostat Physical Properties
Melting Point 148°C
Boiling Point 315.6±44.0 °C
inventory_2 Storage & Handling
Density 2.11±0.1 g/cm3
Storage -20°C, sealed, light-proof, inert gas

description Product Description

Used in bioconjugation for site-specific labeling of cysteine residues in proteins and peptides. The iodoacetate group reacts selectively with thiol groups, forming a stable thioether bond, while the NHS ester enables coupling to primary amines. Commonly applied in preparing fluorescent or biotinylated probes for imaging, detection, and pull-down assays. Also utilized in crosslinking studies and targeted drug delivery systems where precise attachment to sulfhydryl groups is required. Stable under physiological conditions, making it suitable for labeling biomolecules in mild buffers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,320.00
inventory 100mg
10-20 days ฿3,410.00
inventory 1g
10-20 days ฿17,820.00
inventory 250mg
10-20 days ฿6,480.00
N-Succinimidyl Iodoacetate
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Used in bioconjugation for site-specific labeling of cysteine residues in proteins and peptides. The iodoacetate group reacts selectively with thiol groups, forming a stable thioether bond, while the NHS ester enables coupling to primary amines. Commonly applied in preparing fluorescent or biotinylated probes for imaging, detection, and pull-down assays. Also utilized in crosslinking studies and targeted drug delivery systems where precise attachment to sulfhydryl groups is required. Stable under physiol

Used in bioconjugation for site-specific labeling of cysteine residues in proteins and peptides. The iodoacetate group reacts selectively with thiol groups, forming a stable thioether bond, while the NHS ester enables coupling to primary amines. Commonly applied in preparing fluorescent or biotinylated probes for imaging, detection, and pull-down assays. Also utilized in crosslinking studies and targeted drug delivery systems where precise attachment to sulfhydryl groups is required. Stable under physiological conditions, making it suitable for labeling biomolecules in mild buffers.

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