21-[(tert-Butoxycarbonyl)amino]-4,7,10,13,16,19-hexaoxaheneicosanoic Acid

98%

Reagent Code: #78620
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CAS Number 882847-13-4

science Other reagents with same CAS 882847-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 453.53 g/mol
Formula C₂₀H₃₉NO₁₀
badge Registry Numbers
MDL Number MFCD07781255
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily used in the field of bioconjugation and peptide synthesis. It serves as a linker molecule, facilitating the attachment of various biomolecules, such as peptides or proteins, to other substrates or surfaces. Its structure, featuring both a Boc-protected amino group and a carboxylic acid group, allows for controlled and selective reactions, making it valuable in creating complex molecular architectures. Additionally, its polyethylene glycol (PEG) spacer enhances solubility and reduces steric hindrance, which is particularly useful in developing drug delivery systems and bioconjugates for therapeutic applications. It is also employed in surface modification techniques, enabling the functionalization of materials for biomedical research and diagnostics.

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Test Parameter Specification
Appearance Colorless to Light Yellow to Yellow-Brown Oil
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,015.00

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21-[(tert-Butoxycarbonyl)amino]-4,7,10,13,16,19-hexaoxaheneicosanoic Acid
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This compound is primarily used in the field of bioconjugation and peptide synthesis. It serves as a linker molecule, facilitating the attachment of various biomolecules, such as peptides or proteins, to other substrates or surfaces. Its structure, featuring both a Boc-protected amino group and a carboxylic acid group, allows for controlled and selective reactions, making it valuable in creating complex molecular architectures. Additionally, its polyethylene glycol (PEG) spacer enhances solubility and re

This compound is primarily used in the field of bioconjugation and peptide synthesis. It serves as a linker molecule, facilitating the attachment of various biomolecules, such as peptides or proteins, to other substrates or surfaces. Its structure, featuring both a Boc-protected amino group and a carboxylic acid group, allows for controlled and selective reactions, making it valuable in creating complex molecular architectures. Additionally, its polyethylene glycol (PEG) spacer enhances solubility and reduces steric hindrance, which is particularly useful in developing drug delivery systems and bioconjugates for therapeutic applications. It is also employed in surface modification techniques, enabling the functionalization of materials for biomedical research and diagnostics.

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