Aminooxy-peg4-t-butyl ester

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Reagent Code: #107619
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CAS Number 2100306-82-7

science Other reagents with same CAS 2100306-82-7

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Weight 337.41 g/mol
Formula C₁₅H₃₁NO₇
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MDL Number MFCD30730368
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Aminooxy-PEG4-t-butyl ester is widely used in bioconjugation and chemical biology research. Its primary application involves linking biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The aminooxy group reacts selectively with aldehydes or ketones, forming stable oxime bonds, while the PEG4 spacer enhances solubility and reduces steric hindrance. This makes it valuable for creating targeted drug delivery systems, diagnostic probes, and functionalized biomaterials. The t-butyl ester group provides protection during synthesis, which can be removed under specific conditions to expose a carboxylic acid for further modifications. Its versatility and efficiency make it a key reagent in developing advanced bioconjugates for therapeutic and diagnostic applications.

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inventory 1g
10-20 days ฿123,417.00

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Aminooxy-peg4-t-butyl ester
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Aminooxy-PEG4-t-butyl ester is widely used in bioconjugation and chemical biology research. Its primary application involves linking biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The aminooxy group reacts selectively with aldehydes or ketones, forming stable oxime bonds, while the PEG4 spacer enhances solubility and reduces steric hindrance. This makes it valuable for creating targeted drug delivery systems, diagnostic probes, and functionalized biomaterials. Th

Aminooxy-PEG4-t-butyl ester is widely used in bioconjugation and chemical biology research. Its primary application involves linking biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The aminooxy group reacts selectively with aldehydes or ketones, forming stable oxime bonds, while the PEG4 spacer enhances solubility and reduces steric hindrance. This makes it valuable for creating targeted drug delivery systems, diagnostic probes, and functionalized biomaterials. The t-butyl ester group provides protection during synthesis, which can be removed under specific conditions to expose a carboxylic acid for further modifications. Its versatility and efficiency make it a key reagent in developing advanced bioconjugates for therapeutic and diagnostic applications.

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