Azidoethyl-SS-propionic NHS ester - CAS 2243566-44-9

Azidoethyl-SS-propionic NHS ester - CAS 2243566-44-9 Catalog number: BADC-01088

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Category
ADCs Linker
Product Name
Azidoethyl-SS-propionic NHS ester
CAS
2243566-44-9
Catalog Number
BADC-01088
Molecular Formula
C9H12N4O4S2
Molecular Weight
304.35
Azidoethyl-SS-propionic NHS ester

Ordering Information

Catalog Number Size Price Quantity
BADC-01088 -- $--
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Synonyms
2,5-dioxopyrrolidin-1-yl 3-[(2-azidoethyl)disulfanyl]propanoate
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)CCSSCCN=[N+]=[N-]
InChI
InChI=1S/C9H12N4O4S2/c10-12-11-4-6-19-18-5-3-9(16)17-13-7(14)1-2-8(13)15/h1-6H2
InChIKey
KEOGJOSSYXNLNK-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Purity
>98.0%
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.

Azidoethyl-SS-propionic NHS ester, a bifunctional crosslinker, finds diverse applications in biochemical and molecular biology settings. Here are four key applications of this compound, presented with high perplexity and burstiness:

Protein Crosslinking: Employing Azidoethyl-SS-propionic NHS ester, researchers forge covalent links between proteins, facilitating the exploration of intricate protein-protein interactions. By crosslinking proteins within a complex, scientists stabilize transient interactions, setting the stage for in-depth analysis. This process is paramount for unraveling interaction partners and deciphering the complexities of protein interaction networks.

Bioconjugation: Widely utilized in bioconjugation, Azidoethyl-SS-propionic NHS ester serves as a versatile tool for attaching biomolecules like peptides or antibodies to diverse surfaces or molecules. Its NHS ester group interacts with amines, enabling targeted modifications of proteins and peptides. This application plays a pivotal role in constructing functionalized surfaces for advanced biosensors and precision-targeted drug delivery systems.

Click Chemistry: A cornerstone in bioorthogonal “click” chemistry, Azidoethyl-SS-propionic NHS ester facilitates the specific and efficient conjugation of biomolecules. The azide group undergoes a copper-catalyzed alkyne-azide cycloaddition reaction, empowering the rapid labeling or immobilization of various biomolecules. This methodology is widely embraced for tagging proteins, nucleic acids, and other biomolecules, catering to diverse imaging and analytical needs.

Fluorescent Labeling: Azidoethyl-SS-propionic NHS ester emerges as a powerful tool for fluorescently labeling proteins and biomolecules, enhancing their visualization in various biological contexts. By introducing azide groups onto biomolecules, researchers can subsequently affix fluorescent probes through click chemistry. This strategy enables real-time tracking and visualization of biomolecules in live cells and in vitro assays, offering valuable insights into dynamic biological processes.

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

Historical Records: Azidoethyl-SS-propionic NHS ester
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