Azido-PEG2-amine - CAS 166388-57-4

Azido-PEG2-amine - CAS 166388-57-4 Catalog number: BADC-00983

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Azido-PEG2-C2-amine (N3-PEG2-CH2CH2NH2) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG2-C2-amine is also a non-cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
Azido-PEG2-amine
CAS
166388-57-4
Catalog Number
BADC-00983
Molecular Formula
C6H14N4O2
Molecular Weight
174.20
Purity
≥95%
Azido-PEG2-amine

Ordering Information

Catalog Number Size Price Quantity
BADC-00983 -- $-- Inquiry
Description
Azido-PEG2-C2-amine (N3-PEG2-CH2CH2NH2) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Azido-PEG2-C2-amine is also a non-cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Synonyms
Azide-PEG3-Amine;2-[2-(2-Azidoethoxy)ethoxy]ethanamine; Azido-PEG2-C2-amine; N3-PEG2-CH2CH2NH2
IUPAC Name
2-[2-(2-azidoethoxy)ethoxy]ethanamine
Canonical SMILES
C(COCCOCCN=[N+]=[N-])N
InChI
InChI=1S/C6H14N4O2/c7-1-3-11-5-6-12-4-2-9-10-8/h1-7H2
InChIKey
ZHWGWSYNZIZTFL-UHFFFAOYSA-N
Solubility
Soluble in Chloroform, Dichloromethane (Slightly)
LogP
0.44166
PSA
94.23000
Appearance
Yellow Oily Matter
Shipping
Room temperature, or blue ice upon request.
Storage
Store at 2-8°C under inert atmosphere
Pictograms
Corrosive
Signal Word
Danger
Form
Liquid

Azido-PEG2-amine, a versatile compound utilized in bioconjugation and biochemistry, holds vast potential for diverse applications. Here are four key applications of Azido-PEG2-amine, conveyed with elevated levels of perplexity and burstiness:

Click Chemistry: Embraced in the realm of click chemistry, Azido-PEG2-amine serves as a linchpin for bioorthogonal labeling and conjugation reactions. The azide group intricately interacts with alkyne-containing molecules via the Huisgen cycloaddition, culminating in the formation of stable triazole linkages. This transformative chemistry enables the precise and selective attachment of biomolecules for a spectrum of uses, spanning from diagnostic imaging to therapeutic interventions.

Drug Delivery Systems: Within the realm of pharmaceutical innovation, Azido-PEG2-amine plays a pivotal role in enhancing drug delivery systems by improving solubility and biocompatibility. The integration of the PEG segment elevates the drug's pharmacokinetics by augmenting its hydrophilicity and prolonging its circulation time in the bloodstream. Leveraging the azido group for further functionalization allows for the conjugation of therapeutic agents, thereby enabling targeted and efficacious drug delivery strategies.

Protein Modification: In the dynamic domain of proteomics, Azido-PEG2-amine emerges as a key player in protein modification through site-specific labeling. By introducing the azide group into proteins using either chemical or enzymatic approaches, researchers pave the way for subsequent conjugation with alkyne-tagged probes. This methodology empowers scientists to delve into protein interactions, monitor localization, and track post-translational modifications with precision and depth.

Surface Functionalization: Azido-PEG2-amine finds its niche in the field of surface functionalization, where it contributes to enhancing the properties of nanoparticles, biosensors, and biomaterials. The strategic coupling of the azide group with alkyne-modified surfaces results in the creation of biocompatible coatings, thereby bolstering the performance of materials. This heightened functionality opens up new avenues for applications in medical devices, tissue engineering, and diagnostic tools, ushering in a wave of innovation and advancement in diverse sectors.

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: Azido-PEG2-amine
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