Tetra(-amido-dPEG®11-MAL)pentaerythritol, product number 11435, is a maleimide-functionalized click chemistry reagent designed to crosslink up to four molecules via a thiol-maleimide reaction. Built around a pentaerythritol core, each arm of this four-branched molecule consists of a single molecular weight, discrete polyethylene glycol (dPEG®) spacer functionalized with a maleimidopropyl group. Each of the four (4) equal-length dPEG®11 arms are from the pentaerythritol core to the reactive site on the maleimide. 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 mixture 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. Our What is dPEG®? page provides more information on our technology. For answers to our frequently asked questions, please click here.
Tetra(-amido-dPEG®11-MAL)pentaerythritol showcases the value of dPEG® in constructing useful products. Each of the four dPEG® arms extending from the pentaerythritol core is the same length. All four 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 our Maleimide Reaction Chemistry page.
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.
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.