Cbz-NH-PEG1-CH2CH2COOH

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Reagent Code: #106140
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CAS Number 1205751-19-4

science Other reagents with same CAS 1205751-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.28 g/mol
Formula C₁₃H₁₇NO₅
badge Registry Numbers
MDL Number MFCD14582436
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily used in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of peptides or other biomolecules to various surfaces or carriers. The Cbz (carboxybenzyl) group acts as a protective group for amines, which can be selectively removed during synthesis. The PEG (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, making it useful in drug delivery systems. The carboxyl group at the end allows for further functionalization, such as coupling with amines or other reactive groups, facilitating the creation of complex molecular structures. Its applications are particularly valuable in developing targeted therapies, diagnostic tools, and biomaterials.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿9,090.00
inventory 5mg
10-20 days ฿30,060.00

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Cbz-NH-PEG1-CH2CH2COOH
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This chemical is primarily used in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of peptides or other biomolecules to various surfaces or carriers. The Cbz (carboxybenzyl) group acts as a protective group for amines, which can be selectively removed during synthesis. The PEG (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, making it useful in drug delivery systems. The carboxyl group at the end allows for

This chemical is primarily used in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of peptides or other biomolecules to various surfaces or carriers. The Cbz (carboxybenzyl) group acts as a protective group for amines, which can be selectively removed during synthesis. The PEG (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, making it useful in drug delivery systems. The carboxyl group at the end allows for further functionalization, such as coupling with amines or other reactive groups, facilitating the creation of complex molecular structures. Its applications are particularly valuable in developing targeted therapies, diagnostic tools, and biomaterials.

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