Fmoc-NH-ethyl-SS-propionic NHS ester - CAS 2128735-23-7

Fmoc-NH-ethyl-SS-propionic NHS ester - CAS 2128735-23-7 Catalog number: BADC-01071

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Category
ADCs Linker
Product Name
Fmoc-NH-ethyl-SS-propionic NHS ester
CAS
2128735-23-7
Catalog Number
BADC-01071
Molecular Formula
C24H24N2O6S2
Molecular Weight
500.59
Purity
>98.0%

Ordering Information

Catalog Number Size Price Quantity
BADC-01071 -- $-- Inquiry
Synonyms
2,5-dioxopyrrolidin-1-yl 3-((2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)ethyl)disulfanyl)propanoate
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)CCSSCCNC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
InChI
InChI=1S/C24H24N2O6S2/c27-21-9-10-22(28)26(21)32-23(29)11-13-33-34-14-12-25-24(30)31-15-20-18-7-3-1-5-16(18)17-6-2-4-8-19(17)20/h1-8,20H,9-15H2,(H,25,30)
InChIKey
XTOJUNPXMJPADI-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -20 °C, keep in dry and avoid sunlight.

Fmoc-NH-ethyl-SS-propionic NHS ester, a versatile reagent in peptide synthesis and conjugation chemistry, finds wide-ranging applications. Here are four key uses:

Peptide Synthesis: Playing a pivotal role in solid-phase peptide synthesis, Fmoc-NH-ethyl-SS-propionic NHS ester is crucial for safeguarding and activating amino groups. This compound ensures the stable attachment of amino acids while mitigating undesired side reactions. Its gentle cleavage conditions preserve the integrity of the synthesized peptide, allowing for the precise construction of peptide sequences with high efficiency.

Protein Conjugation: In the realm of protein modification, this NHS ester emerges as a versatile tool for conjugating proteins with diverse functional groups, including fluorescent dyes, drugs, or other biomolecules. Through its reaction with primary amines on proteins, it forms robust amide bonds, facilitating the generation of bioconjugates for applications spanning imaging, diagnostics, and targeted therapies.

Surface Modification: Stepping into the domain of surface functionalization, Fmoc-NH-ethyl-SS-propionic NHS ester acts as a potent agent for attaching bioactive molecules to surfaces. By binding to amine groups on substrates, this reagent enables the modification of surfaces with peptides, antibodies, or polymers. This application holds substantial value for crafting biosensors, biomaterials, and tissue engineering scaffolds, offering a versatile platform for tailored surface engineering solutions.

Nucleic Acid Labeling: Transitioning to nucleic acid labeling, this compound proves instrumental in labeling nucleic acids by binding to amino-modified oligonucleotides or nucleotides. The resultant labeled nucleic acids find diverse applications in molecular biology, including hybridization assays, sequencing, and fluorescence-based detection methods. This labeling strategy enhances the sensitivity and specificity of nucleic acid-based techniques, empowering researchers with powerful tools for molecular analysis and manipulation.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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