N-(Tos-peg4)-n-bis(peg4-t-butyl ester)

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Reagent Code: #55271
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CAS Number 2112737-74-1

science Other reagents with same CAS 2112737-74-1

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scatter_plot Molecular Information
Weight 956.1900000000001 g/mol
Formula C₄₅H₈₁NO₁₈S
badge Registry Numbers
MDL Number MFCD30828699
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical, N-(Tos-PEG4)-N-bis(PEG4-t-butyl ester), is a branched PEG linker primarily utilized in bioconjugation and drug delivery systems. Its structure features a central nitrogen atom connected to one tosyl-activated PEG4 chain and two PEG4 chains terminated with t-butyl ester groups. The PEG chains enhance solubility, stability, and biocompatibility, while the tosyl group serves as a reactive leaving group for selective and efficient conjugation reactions with nucleophiles like thiols or amines on biomolecules such as proteins, peptides, or antibodies. The t-butyl ester groups act as protected carboxylic acids, allowing for further functionalization or deprotection in synthetic routes. It is often employed in the development of targeted therapies for precise drug delivery to specific cells or tissues. Additionally, its use in modifying surfaces or nanoparticles improves biocompatibility and reduces immunogenicity, making it valuable in biomedical research and therapeutic applications.

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inventory 1g
10-20 days ฿118,881.00

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N-(Tos-peg4)-n-bis(peg4-t-butyl ester)
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This chemical, N-(Tos-PEG4)-N-bis(PEG4-t-butyl ester), is a branched PEG linker primarily utilized in bioconjugation and drug delivery systems. Its structure features a central nitrogen atom connected to one tosyl-activated PEG4 chain and two PEG4 chains terminated with t-butyl ester groups. The PEG chains enhance solubility, stability, and biocompatibility, while the tosyl group serves as a reactive leaving group for selective and efficient conjugation reactions with nucleophiles like thiols or amines o

This chemical, N-(Tos-PEG4)-N-bis(PEG4-t-butyl ester), is a branched PEG linker primarily utilized in bioconjugation and drug delivery systems. Its structure features a central nitrogen atom connected to one tosyl-activated PEG4 chain and two PEG4 chains terminated with t-butyl ester groups. The PEG chains enhance solubility, stability, and biocompatibility, while the tosyl group serves as a reactive leaving group for selective and efficient conjugation reactions with nucleophiles like thiols or amines on biomolecules such as proteins, peptides, or antibodies. The t-butyl ester groups act as protected carboxylic acids, allowing for further functionalization or deprotection in synthetic routes. It is often employed in the development of targeted therapies for precise drug delivery to specific cells or tissues. Additionally, its use in modifying surfaces or nanoparticles improves biocompatibility and reduces immunogenicity, making it valuable in biomedical research and therapeutic applications.

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