tert-Butyl (6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexyl)carbamate

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Reagent Code: #87832
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CAS Number 124529-64-2

science Other reagents with same CAS 124529-64-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.36 g/mol
Formula C₁₅H₂₄N₂O₄
badge Registry Numbers
MDL Number MFCD22683316
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used in the field of bioconjugation and protein modification. It serves as a linker or spacer molecule in the synthesis of peptide and protein conjugates. The presence of the reactive pyrrole dione group allows it to form stable covalent bonds with thiol groups in proteins, making it valuable for labeling or functionalizing biomolecules. It is often employed in the development of antibody-drug conjugates (ADCs), where it helps connect therapeutic agents to antibodies for targeted drug delivery. Additionally, it is utilized in the preparation of biomaterials and hydrogels for applications in tissue engineering and drug delivery systems. Its stability and reactivity make it a versatile tool in biochemical research and pharmaceutical development.

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inventory 1g
10-20 days ฿23,778.00

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tert-Butyl (6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexyl)carbamate
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This chemical is primarily used in the field of bioconjugation and protein modification. It serves as a linker or spacer molecule in the synthesis of peptide and protein conjugates. The presence of the reactive pyrrole dione group allows it to form stable covalent bonds with thiol groups in proteins, making it valuable for labeling or functionalizing biomolecules. It is often employed in the development of antibody-drug conjugates (ADCs), where it helps connect therapeutic agents to antibodies for target

This chemical is primarily used in the field of bioconjugation and protein modification. It serves as a linker or spacer molecule in the synthesis of peptide and protein conjugates. The presence of the reactive pyrrole dione group allows it to form stable covalent bonds with thiol groups in proteins, making it valuable for labeling or functionalizing biomolecules. It is often employed in the development of antibody-drug conjugates (ADCs), where it helps connect therapeutic agents to antibodies for targeted drug delivery. Additionally, it is utilized in the preparation of biomaterials and hydrogels for applications in tissue engineering and drug delivery systems. Its stability and reactivity make it a versatile tool in biochemical research and pharmaceutical development.

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