Catalog Number
ACM401916618-3
Product Name
O-[2-(3-Mercaptopropionylamino)ethyl]-O'-methylpolyethylene glycol
Category
Poly(ethylene glycol) and Poly(ethylene oxide)
Synonyms
PEG-thiol, 'Mercaptopolyethylene glycol monomethyl ether'
Description
Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation.
IUPAC Name
2-methoxyethanol;2-(2-sulfanylethoxy)ethanol
Molecular Weight
198.28g/mol
Molecular Formula
C7H18O4S
Canonical SMILES
COCCO.C(COCCS)O
InChI
InChI=1S/C4H10O2S.C3H8O2/c5-1-2-6-3-4-7;1-5-3-2-4/h5,7H,1-4H2;4H,2-3H2,1H3
InChI Key
PVYJAAVBEMPGMU-UHFFFAOYSA-N
Application
Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity.
Covalently-Bonded Unit Count
2
Features And Benefits
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3. Additional products can be ordered, please contact us for details
Monoisotopic Mass
198.09258g/mol