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Cl-PEG8-acid

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Category Cl-PEGn-acid
Catalog NO. BPG-1535
Product Name Cl-PEG8-acid
Molecular Formula C19H37ClO10
Molecular Weight 460.95
Cl-PEG8-acid
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Product Information

Synonyms Cl-PEG8-CH2CH2COOH; 1-chloro-3,6,9,12,15,18,21,24-octaoxaheptacosan-27-oic acid
IUPAC Name 3-[2-[2-[2-[2-[2-[2-[2-(2-chloroethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid
Canonical SMILES O=C(O)CCOCCOCCOCCOCCOCCOCCOCCOCCCl
InChI InChI=1S/C19H37ClO10/c20-2-4-24-6-8-26-10-12-28-14-16-30-18-17-29-15-13-27-11-9-25-7-5-23-3-1-19(21)22/h1-18H2,(H,21,22)
InChIKey LQNLLUMELGWSLE-UHFFFAOYSA-N
Purity ≥95%
Storage Store at 2-8°C

Cl-PEG8-acid, a derivatized polyethylene glycol compound with a chloride and carboxylic acid functional group, has become increasingly significant in various scientific and industrial applications. One of its primary applications is in bioconjugation. The carboxylic acid group is particularly reactive with amine groups on proteins, peptides, or other molecules, enabling the formation of stable amide bonds. This capability is crucial for developing targeted drug delivery systems where pharmaceuticals are conjugated to specific targeting moieties like antibodies or peptides. The PEG moiety, with its eight ethylene glycol units, imparts water solubility and biocompatibility, reducing immunogenicity and enhancing the pharmacokinetic properties of bioconjugates.

Another key application of Cl-PEG8-acid is in the field of surface modification, particularly for the development of anti-fouling surfaces. The PEG chains are known for their ability to resist protein adsorption and cell adhesion due to their hydrophilic nature and mobility. By creating self-assembled monolayers (SAMs) on surfaces such as glass, gold, or silicon, Cl-PEG8-acid can effectively reduce nonspecific binding in biosensor applications or medical implants. This reduces the risk of biofilm formation and enhances the reliability and lifespan of various biomedical devices. The chloride group provides a straightforward handle for functionalization on different surfaces, expanding its utility across numerous materials and applications.

In the realm of nanoparticle functionalization, Cl-PEG8-acid plays a pivotal role. Its carboxylic acid end can react with nanoparticle surfaces that have active amine groups or can be activated for other coupling chemistries. By attaching PEG chains to nanoparticles, one can significantly enhance their dispersion stability in biological media, reduce opsonization by the immune system, and prolong the circulation time of the nanoparticles in vivo. This is particularly important for applications in drug delivery, imaging, and diagnostics, where the functionalized nanoparticles can be engineered to target specific tissues or cells while avoiding rapid clearance from the body.

Furthermore, Cl-PEG8-acid is utilized in the synthesis of dendrimers and macromolecular structures. Dendrimers are highly branched, tree-like structures with numerous surface functional groups that can be used for drug delivery, gene therapy, or as catalysts. The PEG chains in Cl-PEG8-acid can help modify the outer layer of these dendrimers, enhancing their solubility and biocompatibility and providing a means to attach various functional groups including therapeutic agents or targeting ligands. This versatility enables the creation of highly specialized molecules tailored for specific therapeutic or diagnostic applications, leveraging the benefits of both PEGylation and dendrimer architecture.

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PEGylation of Peptides and Proteins

PEGylation of Peptides
and Proteins

Reduce the Immunogenicity of Peptide/Protein Drugs

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