2,5-Dioxopyrrolidin-1-yl docosanoate

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Reagent Code: #40896
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CAS Number 58047-86-2

science Other reagents with same CAS 58047-86-2

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Weight 437.6557 g/mol
Formula C₂₆H₄₇NO₄
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2,5-Dioxopyrrolidin-1-yl docosanoate is the N-hydroxysuccinimide (NHS) ester of docosanoic acid (behenic acid), a reactive lipid reagent. It is primarily used in bioconjugation chemistry to covalently attach a C22 alkyl chain to primary amines on proteins, peptides, antibodies, and other biomolecules. This lipidation increases hydrophobicity, enables membrane anchoring, and enhances stability in liposomal or nanoparticle formulations. Key applications include targeted drug delivery systems, improving solubility, bioavailability, and efficacy of therapeutics. Its biocompatibility and selective reactivity make it ideal for biomedical research and pharmaceutical development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,177.00

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2,5-Dioxopyrrolidin-1-yl docosanoate
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2,5-Dioxopyrrolidin-1-yl docosanoate is the N-hydroxysuccinimide (NHS) ester of docosanoic acid (behenic acid), a reactive lipid reagent. It is primarily used in bioconjugation chemistry to covalently attach a C22 alkyl chain to primary amines on proteins, peptides, antibodies, and other biomolecules. This lipidation increases hydrophobicity, enables membrane anchoring, and enhances stability in liposomal or nanoparticle formulations. Key applications include targeted drug delivery systems, improving sol

2,5-Dioxopyrrolidin-1-yl docosanoate is the N-hydroxysuccinimide (NHS) ester of docosanoic acid (behenic acid), a reactive lipid reagent. It is primarily used in bioconjugation chemistry to covalently attach a C22 alkyl chain to primary amines on proteins, peptides, antibodies, and other biomolecules. This lipidation increases hydrophobicity, enables membrane anchoring, and enhances stability in liposomal or nanoparticle formulations. Key applications include targeted drug delivery systems, improving solubility, bioavailability, and efficacy of therapeutics. Its biocompatibility and selective reactivity make it ideal for biomedical research and pharmaceutical development.

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