4-(N-Succinimidylcarboxy)benzophenone

98%,LC&N

Reagent Code: #217376
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CAS Number 91990-88-4

science Other reagents with same CAS 91990-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.3 g/mol
Formula C₁₈H₁₃NO₅
badge Registry Numbers
MDL Number MFCD00058572
thermostat Physical Properties
Melting Point 205-206°C
Boiling Point 501.5°C
inventory_2 Storage & Handling
Density 1.4g/cm3
Storage -20°C, inert gas environment

description Product Description

Used primarily as a photoactivatable crosslinking agent in biochemical and biophysical research. It enables covalent bonding between biomolecules such as proteins, peptides, and nucleic acids upon exposure to UV light. The compound is especially valuable in studying molecular interactions, as it can capture transient or weak interactions in complex biological systems. Commonly conjugated to amine-containing molecules via its NHS ester group, it allows for site-specific labeling and immobilization on surfaces or within matrices. Widely applied in proteomics, receptor-ligand studies, and the development of biosensors and diagnostic assays.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿790.00
100mg
10-20 days ฿1,200.00
250mg
10-20 days ฿2,160.00
1g
10-20 days ฿7,800.00
4-(N-Succinimidylcarboxy)benzophenone
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Used primarily as a photoactivatable crosslinking agent in biochemical and biophysical research. It enables covalent bonding between biomolecules such as proteins, peptides, and nucleic acids upon exposure to UV light. The compound is especially valuable in studying molecular interactions, as it can capture transient or weak interactions in complex biological systems. Commonly conjugated to amine-containing molecules via its NHS ester group, it allows for site-specific labeling and immobilization on surf

Used primarily as a photoactivatable crosslinking agent in biochemical and biophysical research. It enables covalent bonding between biomolecules such as proteins, peptides, and nucleic acids upon exposure to UV light. The compound is especially valuable in studying molecular interactions, as it can capture transient or weak interactions in complex biological systems. Commonly conjugated to amine-containing molecules via its NHS ester group, it allows for site-specific labeling and immobilization on surfaces or within matrices. Widely applied in proteomics, receptor-ligand studies, and the development of biosensors and diagnostic assays.

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