N-Boc-N-bis(PEG2-OH)

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Reagent Code: #106377
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CAS Number 275385-03-0

science Other reagents with same CAS 275385-03-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₃H₂₇NO₆
badge Registry Numbers
MDL Number MFCD30723207
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is widely used in the field of bioconjugation and drug delivery systems. Its structure, featuring PEG (polyethylene glycol) chains and a Boc (tert-butoxycarbonyl) protecting group, makes it highly suitable for modifying peptides, proteins, and other biomolecules. The PEG chains enhance solubility and stability, while the Boc group allows for controlled deprotection during synthesis. It is particularly valuable in creating linkers for antibody-drug conjugates (ADCs) and in developing targeted therapeutic agents. Additionally, its biocompatibility and ability to reduce immunogenicity make it a preferred choice in pharmaceutical research and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿36,000.00
inventory 250mg
10-20 days ฿55,800.00

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N-Boc-N-bis(PEG2-OH)
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This chemical is widely used in the field of bioconjugation and drug delivery systems. Its structure, featuring PEG (polyethylene glycol) chains and a Boc (tert-butoxycarbonyl) protecting group, makes it highly suitable for modifying peptides, proteins, and other biomolecules. The PEG chains enhance solubility and stability, while the Boc group allows for controlled deprotection during synthesis. It is particularly valuable in creating linkers for antibody-drug conjugates (ADCs) and in developing targete

This chemical is widely used in the field of bioconjugation and drug delivery systems. Its structure, featuring PEG (polyethylene glycol) chains and a Boc (tert-butoxycarbonyl) protecting group, makes it highly suitable for modifying peptides, proteins, and other biomolecules. The PEG chains enhance solubility and stability, while the Boc group allows for controlled deprotection during synthesis. It is particularly valuable in creating linkers for antibody-drug conjugates (ADCs) and in developing targeted therapeutic agents. Additionally, its biocompatibility and ability to reduce immunogenicity make it a preferred choice in pharmaceutical research and development.

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