N-(4-Nitrophenyl)maleimide

≥98%

Reagent Code: #121396
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CAS Number 4338-06-1

science Other reagents with same CAS 4338-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.17 g/mol
Formula C₁₀H₆N₂O₄
badge Registry Numbers
MDL Number MFCD00022576
thermostat Physical Properties
Melting Point 169-172°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

N-(4-Nitrophenyl)maleimide is widely used in organic synthesis as a building block for creating complex molecules. Its maleimide group reacts with thiols, making it useful for forming thioether linkages in peptides and proteins. In polymer chemistry, it acts as a crosslinking agent to improve the mechanical and thermal properties of polymers. It is also employed in bioconjugation to attach labels or functional groups to biomolecules for biochemical assays and diagnostics. In material science, it introduces nitro groups into polymers or other materials for use in sensors or coatings. Additionally, it serves as a reagent in research studies to investigate reaction mechanisms involving maleimide and nitro group chemistry.

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Test Parameter Specification
APPEARANCE White to Light yellow to Green powder to crystal
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿2,277.00

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N-(4-Nitrophenyl)maleimide
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N-(4-Nitrophenyl)maleimide is widely used in organic synthesis as a building block for creating complex molecules. Its maleimide group reacts with thiols, making it useful for forming thioether linkages in peptides and proteins. In polymer chemistry, it acts as a crosslinking agent to improve the mechanical and thermal properties of polymers. It is also employed in bioconjugation to attach labels or functional groups to biomolecules for biochemical assays and diagnostics. In material science, it introduc

N-(4-Nitrophenyl)maleimide is widely used in organic synthesis as a building block for creating complex molecules. Its maleimide group reacts with thiols, making it useful for forming thioether linkages in peptides and proteins. In polymer chemistry, it acts as a crosslinking agent to improve the mechanical and thermal properties of polymers. It is also employed in bioconjugation to attach labels or functional groups to biomolecules for biochemical assays and diagnostics. In material science, it introduces nitro groups into polymers or other materials for use in sensors or coatings. Additionally, it serves as a reagent in research studies to investigate reaction mechanisms involving maleimide and nitro group chemistry.

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