N-Hydroxysulfosuccinimide sodium salt

98%

Reagent Code: #65726
label
Alias Thiohydroxysuccinimide; Sodium N-Hydroxybutylene Sulfonate; Sodium N-Hydroxysuccinimide Sulfonate; N-Hydroxysulfosuccinimide; N-Hydroxysulfosuccinimide sodium salt
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CAS Number 106627-54-7

science Other reagents with same CAS 106627-54-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.13 g/mol
Formula C₄H₄NNaO₆S
badge Registry Numbers
MDL Number MFCD00043100
thermostat Physical Properties
Melting Point 250 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key reagent in bioconjugation processes, it facilitates the coupling of biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. Commonly employed in the preparation of affinity chromatography resins, it helps immobilize ligands onto solid supports for protein purification. It is also utilized in the synthesis of active esters for peptide coupling reactions, enhancing the efficiency of amide bond formation. In diagnostic applications, it aids in the labeling of antibodies and proteins with fluorescent dyes or other markers for detection and imaging. Additionally, it plays a role in crosslinking reactions for studying protein-protein interactions and in the development of drug delivery systems.

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Test Parameter Specification
Purity (HPLC) 98-100%
Purity (Ion Exchange Titration) 98-105%
Water (Karl Fischer) 0-4%
Appearance White to yellow powder
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,730.00
inventory 25g
10-20 days ฿23,000.00
inventory 1g
10-20 days ฿1,020.00

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N-Hydroxysulfosuccinimide sodium salt
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Used as a key reagent in bioconjugation processes, it facilitates the coupling of biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. Commonly employed in the preparation of affinity chromatography resins, it helps immobilize ligands onto solid supports for protein purification. It is also utilized in the synthesis of active esters for peptide coupling reactions, enhancing the efficiency of amide bond formation. In diagnostic applications, it aids in the labeling of

Used as a key reagent in bioconjugation processes, it facilitates the coupling of biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. Commonly employed in the preparation of affinity chromatography resins, it helps immobilize ligands onto solid supports for protein purification. It is also utilized in the synthesis of active esters for peptide coupling reactions, enhancing the efficiency of amide bond formation. In diagnostic applications, it aids in the labeling of antibodies and proteins with fluorescent dyes or other markers for detection and imaging. Additionally, it plays a role in crosslinking reactions for studying protein-protein interactions and in the development of drug delivery systems.

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