Hexa(-amido-dPEG®11-MAL)dipentaerythritol, product number 11436, is a maleimide-functionalized click chemistry reagent designed to crosslink up to six molecules via a thiol-maleimide reaction. Built around a dipentaerythritol core, each arm of this six-branched molecule consists of a single molecular weight, discrete polyethylene glycol (dPEG®) spacer functionalized with a maleimidopropyl group. Each of the six (6) equal-length dPEG®11 arms are 43 atoms long (47.4 Å) from the dipentaerythritol core to the reactive site on the maleimide. The molecular weight of this product is 4,753 Daltons. Applications for this product include (1) crosslinking of proteins, peptides, or small molecules containing free sulfhydryl groups and (2) dendrimer construction with thiol-functionalized branched compounds.
Traditional polyethylene glycol (PEG) is a disperse polymer. Any given size PEG consists of a multiplicity of different PEG chain lengths, each with a different molecular weight. The stated size of a traditional PEG is an average molecular weight for that mixture. By contrast, Quanta BioDesign’s dPEG® products are not disperse polymers. Each dPEG® product contains a single molecular weight of PEG with a discrete chain length, hence the dPEG® name. For more information on our dPEG® technology, please click this link. For answers to our frequently asked questions, please click here.
Hexa(-amido-dPEG®11-MAL)dipentaerythritol showcases the value of dPEG® in constructing useful products. Each of the six dPEG® arms extending from the dipentaerythritol core is the same length. All six arms are constructed and functionalized identically. Analysis of the product is simplified. This product would not be possible with traditional, disperse PEG.
The thiol-maleimide reaction, also known as the thiol-Michael addition, is a popular, powerful click chemistry reaction. At pH 6.5 – 7.5, the reaction between a sulfhydryl and a maleimide is chemoselective. The maleimide group can react with free amines (for example, lysine) when the pH is greater than 7.5. For more information about the thiol-maleimide reaction, please see Maleimide Reaction Chemistry.
If you need bulk product in a larger package size than our standard sizes, please contact us for a quote. Our commercial capabilities permit us to manufacture this product at any scale that you need.
Hermanson, G. T. Chapter 2, Functional Targets for Bioconjugation. Bioconjugate Techniques, 3rd edition. Academic Press: New York, 2013, 127-228. Want to learn more about Greg’s book? Click here now for a review of Greg’s book and a link to purchase it.
Hermanson, G. T. Chapter 3, The Reactions of Bioconjugation. Bioconjugate Techniques, 3rd edition. Academic Press: New York, 2013, 229-258, specifically page 241, discussing maleimide reactions.
Hermanson, G. T. Chapter 8, Dendrimers and Dendrons. Bioconjugate Techniques, 3rd edition. Academic Press: New York, 2013, 351-386.
Hermanson, G. T. Chapter 18, PEGylation and Synthetic Polymer Modification. Bioconjugate Techniques, 3rd edition. Academic Press: New York, 2013, 787-838.
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