Bis-Propargyl-PEG18

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Bis-Propargyl-PEG18

Bis-Propargyl-PEG18 | 124238-56-8

Catalog Number R01-0139
Category Alkynes
Molecular Formula C40H74O18
Molecular Weight 843.00
Catalog Number Size Price Quantity
R01-0139 -- $--

Product Introduction

Bis-propargyl-PEG18 is a click chemistry reagent.

Chemical Information

Synonyms Bis-propargyl-PEG14
Purity 98%
IUPAC Name 3-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]prop-1-yne
Canonical SMILES C#CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC#C
InChI InChI=1S/C40H74O18/c1-3-5-41-7-9-43-11-13-45-15-17-47-19-21-49-23-25-51-27-29-53-31-33-55-35-37-57-39-40-58-38-36-56-34-32-54-30-28-52-26-24-50-22-20-48-18-16-46-14-12-44-10-8-42-6-4-2/h1-2H,5-40H2
InChI Key HFYDCCREWNLTDR-UHFFFAOYSA-N
Solubility Water, DMSO, DCM, DMF
  • Product Specification
  • Application
Storage -20 °C

Bis-propargyl-PEG18 is a polyethylene glycol (PEG) derivative with terminal propargyl groups, making it highly versatile for various biochemical applications. Here are some key applications of Bis-propargyl-PEG18:

Click Chemistry Reactions: Bis-propargyl-PEG18 is frequently used in click chemistry for bioconjugation purposes. The propargyl groups react efficiently with azides through copper-catalyzed azide-alkyne cycloaddition. This facilitates the rapid and specific labeling of biomolecules, enabling the creation of complex molecular architectures for research and diagnostic applications.

Surface Modification: In material science, Bis-propargyl-PEG18 is employed to modify the surfaces of nanoparticles, polymers, and other substrates. By attaching PEG chains, it helps to improve biocompatibility, reduce non-specific binding, and enhance the stability of surfaces. This is particularly important for creating medical implants, drug delivery systems, and biosensors with reduced immunogenicity and improved performance.

Drug Delivery Systems: Bis-propargyl-PEG18 serves as a linker in the design of drug delivery systems, where it can be used to conjugate therapeutic agents to carrier molecules. The PEG moiety provides solubility and extended circulation times in vivo, while the propargyl groups allow for precise attachment of drugs. This results in targeted and controlled release of therapeutics, potentially improving the efficacy and safety of treatments.

Polymer Crosslinking: Bis-propargyl-PEG18 is utilized in the synthesis of crosslinked polymer networks. The terminal alkyne groups can be engaged in various crosslinking chemistries, such as click reactions or radical polymerization, to form hydrogels and other polymeric structures. These materials can be tailored for specific mechanical properties and are used in applications ranging from tissue engineering scaffolds to responsive drug delivery matrices.

Computed Properties

XLogP3 -2.2
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 18
Rotatable Bond Count 53
Exact Mass 842.48751551 g/mol
Monoisotopic Mass 842.48751551 g/mol
Topological Polar Surface Area 166Ų
Heavy Atom Count 58
Formal Charge 0
Complexity 786
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

Patents

Publication NumberTitlePriority Date
EP-4095128-A1 Tetrahydroquinoline (thq) coumpounds 2021-05-25
WO-2022248475-A1 Tetrahydroquinoline (thq) coumpounds 2021-05-25
US-2021230457-A1 Photocurable adhesion-promoting compositions and methods of use 2020-01-29
WO-2021155092-A1 Photocurable adhesion-promoting compositions and methods of use 2020-01-29
EP-4097182-A1 Photocurable adhesion-promoting compositions and methods of use 2020-01-29
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