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

98%

  • Product Code: 119726
  CAS:    557756-85-1
Molecular Weight: 487.54 g./mol Molecular Formula: C₂₆H₃₃NO₈
EC Number: MDL Number: MFCD06656472
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry and sealed
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.
Product Specification:
Test Specification
Appearance Colorless To Yellow Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿810.00
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0.250 10-20 days ฿1,530.00
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1.000 10-20 days ฿2,570.00
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5.000 10-20 days ฿11,010.00
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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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