1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oic acid

98%

Reagent Code: #119726
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CAS Number 557756-85-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 487.54 g/mol
Formula C₂₆H₃₃NO₈
badge Registry Numbers
MDL Number MFCD06656472
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups or biomolecules to solid supports or other molecules. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable, yet cleavable, connections in complex chemical assemblies. This is especially valuable in the development of targeted drug delivery systems, where precise control over the release of active compounds is crucial. Additionally, it finds application in the synthesis of peptide-based therapeutics, where it aids in the efficient and selective modification of peptide chains, enhancing their stability and bioavailability.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to yellow liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days $60.90
inventory 100mg
10-20 days $32.24
inventory 1g
10-20 days $102.30
inventory 5g
10-20 days $438.25
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oic acid
This compound is primarily utilized in the field of bioconjugation and peptide synthesis. It serves as a versatile linker molecule, enabling the attachment of various functional groups or biomolecules to solid supports or other molecules. Its structure, featuring a fluorenyl group and multiple ether linkages, makes it particularly useful for creating stable, yet cleavable, connections in complex chemical assemblies. This is especially valuable in the development of targeted drug delivery systems, where precise control over the release of active compounds is crucial. Additionally, it finds application in the synthesis of peptide-based therapeutics, where it aids in the efficient and selective modification of peptide chains, enhancing their stability and bioavailability.
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