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Azido-PEG6-amine

  CAS No.: 957486-82-7   Cat No.: BADC-01197   Purity: ≥95% 4.5  

Azido-PEG6-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG6-amine is also a non-cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Azido-PEG6-amine

Structure of 957486-82-7

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Category
ADC Linker
Molecular Formula
C14H30N4O6
Molecular Weight
350.41
Shipping
Room temperature
Shipping
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
O-(2-Aminoethyl)-O'-(2-azidoethyl)pentaethylene Glycol; N3-PEG6-CH2CH2NH2; 20-azido-3,6,9,12,15,18-hexaoxaicosan-1-amine; N3-PEG6-NH2
IUPAC Name
2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine
Canonical SMILES
C(COCCOCCOCCOCCOCCOCCN=[N+]=[N-])N
InChI
InChI=1S/C14H30N4O6/c15-1-3-19-5-7-21-9-11-23-13-14-24-12-10-22-8-6-20-4-2-17-18-16/h1-15H2
InChIKey
VCQSTKKJKNUQBI-UHFFFAOYSA-N
Solubility
Soluble in DCM, DMF, DMSO, Water
PSA
131.15000
Appearance
Pale Yellow or Colorless Oily Matter
Shipping
Room temperature
Storage
Store at -20°C, keep in dry and avoid sunlight
Pictograms
Irritant
Signal Word
Warning
Form
Solid

Azido-PEG6-amine, a versatile compound prized for its unique chemical properties, finds wide applications in bioconjugation and material science. Here are four key applications of Azido-PEG6-amine presented with high perplexity and burstiness:

Bioconjugation: Azido-PEG6-amine plays a pivotal role in linking biomolecules like proteins and peptides through a sophisticated process known as click chemistry. Its azide group selectively reacts with alkyne-modified partners, forging a robust covalent bond. This application is indispensable for advancing biotherapeutics, diagnostic tools, and imaging agents, pushing the boundaries of molecular connectivity.

Drug Delivery: In the realm of drug delivery research, Azido-PEG6-amine shines in modifying the surfaces of nanoparticles and liposomes. This modification boosts the solubility, stability, and biocompatibility of drug carriers, elevating their efficacy to new heights. Moreover, it facilitates targeted delivery to specific tissues or cells, minimizing off-target effects and maximizing therapeutic impact with surgical precision.

Surface Modification: Azido-PEG6-amine finds its niche in functionalizing surfaces in biosensors and medical devices, offering a gateway to enhanced detection and diagnostic accuracy. By anchoring the compound to a surface, researchers can immobilize diverse molecules like antibodies or enzymes, amplifying the sensitivity and specificity of analytical instruments.

Hydrogel Formation: In the realm of material science, Azido-PEG6-amine takes center stage in crafting hydrogels via a sophisticated click chemistry framework. These tailor-made hydrogels are tailored for applications in tissue engineering and regenerative medicine, boasting tunable physical properties and impeccable biocompatibility. They serve as versatile scaffolds that nurture cell growth and instigate tissue regeneration, offering a gateway to a revolutionary approach in biomedical engineering.

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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