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mPEG6-azide

  CAS No.: 1043884-49-6   Cat No.: BADC-00878   Purity: ≥95% 4.5  

mPEG6-azide is a mid-length PEG ADC linker featuring azide functionality for copper-free click chemistry, improving solubility and biocompatibility in antibody-drug conjugates.

mPEG6-azide

Structure of 1043884-49-6

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Category
ADC Linker
Molecular Formula
C13H27N3O6
Molecular Weight
321.37
Shipping
Room temperature
Storage
Store at -20 °C, keep in dry and avoid sunlight.

* For research and manufacturing use only. We do not sell to patients.

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Popular Publications Citing BOC Sciences Products
Synonyms
m-PEG6-azide;19-Azido-2,5,8,11,14,17-hexaoxanonadecane; azido-mPEG6
IUPAC Name
1-azido-2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethane
Canonical SMILES
COCCOCCOCCOCCOCCOCCN=[N+]=[N-]
InChI
InChI=1S/C13H27N3O6/c1-17-4-5-19-8-9-21-12-13-22-11-10-20-7-6-18-3-2-15-16-14/h2-13H2,1H3
InChIKey
MACROZUHOZGXJL-UHFFFAOYSA-N
Solubility
10 mm in DMSO
PSA
105.13000
Appearance
Colorless Liquid
Shelf Life
-20°C 3 years powder; -80°C 2 years in solvent
Shipping
Room temperature
Storage
Store at -20 °C, keep in dry and avoid sunlight.

mPEG6-azide, a polyethylene glycol (PEG) derivative featuring an azide functional group, plays a crucial role in bioconjugation and drug delivery systems. Here are four key applications of mPEG6-azide:

Bioconjugation: Widely utilized in bioconjugation, mPEG6-azide serves as a key component in attaching biomolecules like proteins, peptides, or antibodies to diverse surfaces through copper-catalyzed azide-alkyne cycloaddition (CuAAC), also referred to as “click chemistry”. This method enables the creation of stable, specific linkages in a precise and controlled fashion. The functional versatility of mPEG6-azide renders it an optimal choice for constructing intricate nanostructures tailored for therapeutic and diagnostic purposes.

Drug Delivery Systems: Within advanced drug delivery systems, mPEG6-azide plays a pivotal role in enhancing the solubility and stability of therapeutic agents. By conjugating drugs with mPEG6-azide, researchers can enhance the pharmacokinetics of hydrophilic drugs, resulting in prolonged circulation times and targeted drug delivery.

Surface Modification: mPEG6-azide finds extensive application in surface modification, imparting hydrophilicity and restraining non-specific protein binding on diverse biomaterials. This becomes particularly crucial in the realm of medical devices and biosensors, where mitigating protein adhesion is paramount for optimal device performance and compatibility. Leveraging the azide group of mPEG6-azide enables the adoption of versatile conjugation strategies to tailor surface properties bespoke to specific biomedical requirements, amplifying the potential for innovative design configurations.

Nanoparticle Functionalization: Nanoparticles undergo functionalization with mPEG6-azide to enhance their dispersibility, biocompatibility, and functional adaptability. The presence of azide groups facilitates further functionalization with targeting ligands or imaging agents using click chemistry. This capability stands as a cornerstone for applications in targeted imaging, therapy, and diagnostics, offering enhanced precision over biodistribution and selectivity, marking a significant advancement in nanoparticle customization strategies.

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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