Carbamic acid, N-[(1S)-1-[[[5-(aminooxy)pentyl]amino]carbonyl]-4-[[(dimethylamino)iminomethyl]amino]butyl]-, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl ester

95%

  • Product Code: 65231
  CAS:    1609431-65-3
Molecular Weight: 792.5 g./mol Molecular Formula: C₂₄H₃₃F₁₇N₆O₄
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry, airtight
Product Description: This compound is primarily utilized in the field of biochemistry and molecular biology as a specialized reagent for protein modification. Its unique structure, featuring a perfluorinated tail, allows it to interact with hydrophobic environments, making it suitable for labeling or tagging proteins in complex biological systems. The aminooxy group enables selective conjugation with carbonyl-containing molecules, facilitating the study of protein interactions, localization, and function. Additionally, its application extends to the development of advanced diagnostic tools and targeted drug delivery systems, where precise molecular tagging is essential. The compound’s fluorinated segment also enhances its stability and compatibility with analytical techniques such as mass spectrometry and fluorescence imaging.
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Size (g) Availability Price Quantity
0.100 10-20 days €1,086.52
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Carbamic acid, N-[(1S)-1-[[[5-(aminooxy)pentyl]amino]carbonyl]-4-[[(dimethylamino)iminomethyl]amino]butyl]-, 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl ester
This compound is primarily utilized in the field of biochemistry and molecular biology as a specialized reagent for protein modification. Its unique structure, featuring a perfluorinated tail, allows it to interact with hydrophobic environments, making it suitable for labeling or tagging proteins in complex biological systems. The aminooxy group enables selective conjugation with carbonyl-containing molecules, facilitating the study of protein interactions, localization, and function. Additionally, its application extends to the development of advanced diagnostic tools and targeted drug delivery systems, where precise molecular tagging is essential. The compound’s fluorinated segment also enhances its stability and compatibility with analytical techniques such as mass spectrometry and fluorescence imaging.
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