Fmoc-NH-PEG8-CH2COOH

≥95%

Reagent Code: #106200
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CAS Number 868594-52-9

science Other reagents with same CAS 868594-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 649.73 g/mol
Formula C₃₃H₄₇NO₁₂
badge Registry Numbers
MDL Number MFCD27635163
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a linker or spacer molecule, enabling the attachment of peptides to solid supports. The Fmoc group provides protection for the amine during synthesis, while the PEG8 spacer offers flexibility and solubility, enhancing the efficiency of the reaction. The carboxylic acid group at the end allows for further conjugation or modification of the peptide. It is also employed in bioconjugation, where it facilitates the coupling of peptides or proteins to other molecules, such as drugs, dyes, or polymers, for applications in drug delivery, diagnostics, and biomaterials. Its water-soluble PEG chain improves biocompatibility and reduces immunogenicity, making it suitable for biomedical research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,591.00

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Fmoc-NH-PEG8-CH2COOH
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This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a linker or spacer molecule, enabling the attachment of peptides to solid supports. The Fmoc group provides protection for the amine during synthesis, while the PEG8 spacer offers flexibility and solubility, enhancing the efficiency of the reaction. The carboxylic acid group at the end allows for further conjugation or modification of the peptide. It is also employed in bioconjugation, wh

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a linker or spacer molecule, enabling the attachment of peptides to solid supports. The Fmoc group provides protection for the amine during synthesis, while the PEG8 spacer offers flexibility and solubility, enhancing the efficiency of the reaction. The carboxylic acid group at the end allows for further conjugation or modification of the peptide. It is also employed in bioconjugation, where it facilitates the coupling of peptides or proteins to other molecules, such as drugs, dyes, or polymers, for applications in drug delivery, diagnostics, and biomaterials. Its water-soluble PEG chain improves biocompatibility and reduces immunogenicity, making it suitable for biomedical research.

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