N-Boc-n-bis(peg3-nhs ester)

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Reagent Code: #55472
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CAS Number 2055042-31-2

science Other reagents with same CAS 2055042-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 719.73 g/mol
Formula C₃₁H₄₉N₃O₁₆
badge Registry Numbers
MDL Number MFCD29912756
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used extensively in bioconjugation and peptide synthesis, it serves as a linker to attach polyethylene glycol (PEG) chains to biomolecules. This modification enhances the solubility, stability, and bioavailability of therapeutic proteins, peptides, and other bioactive molecules. It is particularly valuable in drug delivery systems, where PEGylation reduces immunogenicity and prolongs circulation time in the body. Additionally, it is employed in the development of targeted therapies, enabling the precise attachment of functional groups for specific interactions with cellular targets. Its NHS ester groups facilitate efficient coupling with amine-containing compounds, making it a versatile tool in bioconjugation chemistry.

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inventory 250mg
10-20 days ฿52,542.00

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N-Boc-n-bis(peg3-nhs ester)
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Used extensively in bioconjugation and peptide synthesis, it serves as a linker to attach polyethylene glycol (PEG) chains to biomolecules. This modification enhances the solubility, stability, and bioavailability of therapeutic proteins, peptides, and other bioactive molecules. It is particularly valuable in drug delivery systems, where PEGylation reduces immunogenicity and prolongs circulation time in the body. Additionally, it is employed in the development of targeted therapies, enabling the precise

Used extensively in bioconjugation and peptide synthesis, it serves as a linker to attach polyethylene glycol (PEG) chains to biomolecules. This modification enhances the solubility, stability, and bioavailability of therapeutic proteins, peptides, and other bioactive molecules. It is particularly valuable in drug delivery systems, where PEGylation reduces immunogenicity and prolongs circulation time in the body. Additionally, it is employed in the development of targeted therapies, enabling the precise attachment of functional groups for specific interactions with cellular targets. Its NHS ester groups facilitate efficient coupling with amine-containing compounds, making it a versatile tool in bioconjugation chemistry.

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