Propargyl-PEG5-amine
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Category | Small-molecule Heterobifunctional PEG |
Catalog NO. | BPG-1869 |
Product Name | Propargyl-PEG5-amine |
CAS | 1589522-46-2 |
Molecular Formula | C13H25NO5 |
Molecular Weight | 275.34 |
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Description | Propargyl-PEG5-amine is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Propargyl-PEG5-amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. |
Synonyms | Propargyl-PEG5-NH2 |
IUPAC Name | 2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethanamine |
Canonical SMILES | C#CCOCCOCCOCCOCCOCCN |
InChI | InChI=1S/C13H25NO5/c1-2-4-15-6-8-17-10-12-19-13-11-18-9-7-16-5-3-14/h1H,3-14H2 |
InChIKey | BLBTXXAWMPTQOK-UHFFFAOYSA-N |
Boiling Point | 360.4±37.0 °C at 760 mmHg |
Flash Point | 166.5±20.2 °C |
Purity | >98.0% |
Density | 1.0±0.1 g/cm3 |
Solubility | 10 mm in DMSO |
Appearance | Colorless Liquid |
Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
Storage | Store at -5°C,keep in dry and avoid sunlight. |
Vapor Pressure | 0.0±0.8 mmHg at 25°C |
LogP | -1.54 |
Propargyl-PEG5-amine, a versatile bifunctional reagent, plays a pivotal role in biochemical research and pharmaceutical development. Here are four key applications of Propargyl-PEG5-amine presented with high perplexity and burstiness: Bioorthogonal Chemistry: Acting as a cornerstone in bioorthogonal reactions like copper-catalyzed azide-alkyne cycloaddition (CuAAC), Propargyl-PEG5-amine enables the selective conjugation of biomolecules within intricate mixtures, preserving the integrity of native biological processes. This chemistry is indispensable for labeling and tracing biomolecules within the dynamic milieu of live cells and organisms. Drug Delivery Systems: Embraced in drug formulation, Propargyl-PEG5-amine serves as a linchpin in creating prodrug conjugates and sophisticated drug delivery systems. Through PEGylation, which bolsters solubility, stability, and bioavailability of therapeutic agents, researchers can engineer drug-PEG5-amine conjugates via click chemistry, elevating pharmacokinetics and dampening immunogenicity of medicinal compounds. Surface Modification: Employed for the surface alteration of nanoparticles, biosensors, and medical devices, Propargyl-PEG5-amine combines the advantages of the PEG moiety for biocompatibility and the alkyne group for further functionalization through click chemistry. This application is instrumental in crafting cutting-edge diagnostic instruments and ensuring the compatibility of implantable medical devices with biological systems. Proteomics and Glycomics: In the intricate realms of proteomics and glycomics, Propargyl-PEG5-amine stands as a linchpin for targeted tagging of proteins and glycans. By anchoring this reagent to specific functional groups, researchers can meticulously extract and characterize biomolecules from complex samples, offering invaluable insights into protein interactions, glycosylation dynamics, and biomarker discovery. |
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Resources
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Technical Information
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Industry News
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