Ald-Ph-PEG6-acid

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Reagent Code: #64825
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CAS Number 2055013-55-1

science Other reagents with same CAS 2055013-55-1

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Weight 485.52 g/mol
Formula C₂₃H₃₅NO₁₀
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in bioconjugation and drug delivery systems, Ald-Ph-PEG6-acid serves as a heterobifunctional linker molecule featuring an aldehyde group on a phenyl moiety and a terminal carboxylic acid connected by a PEG6 (polyethylene glycol) chain, which enhances solubility and stability. Commonly applied in the development of antibody-drug conjugates (ADCs) and targeted therapies, it facilitates the attachment of drugs or imaging agents to biomolecules like proteins or peptides. The aldehyde group allows for specific reactions with primary amines (e.g., forming Schiff bases), while the carboxylic acid can be activated (e.g., to NHS ester) for amide bond formation. Additionally, it is utilized in surface modification of nanoparticles to improve biocompatibility and reduce immunogenicity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿34,020.00

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Ald-Ph-PEG6-acid
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Used in bioconjugation and drug delivery systems, Ald-Ph-PEG6-acid serves as a heterobifunctional linker molecule featuring an aldehyde group on a phenyl moiety and a terminal carboxylic acid connected by a PEG6 (polyethylene glycol) chain, which enhances solubility and stability. Commonly applied in the development of antibody-drug conjugates (ADCs) and targeted therapies, it facilitates the attachment of drugs or imaging agents to biomolecules like proteins or peptides. The aldehyde group allows for sp

Used in bioconjugation and drug delivery systems, Ald-Ph-PEG6-acid serves as a heterobifunctional linker molecule featuring an aldehyde group on a phenyl moiety and a terminal carboxylic acid connected by a PEG6 (polyethylene glycol) chain, which enhances solubility and stability. Commonly applied in the development of antibody-drug conjugates (ADCs) and targeted therapies, it facilitates the attachment of drugs or imaging agents to biomolecules like proteins or peptides. The aldehyde group allows for specific reactions with primary amines (e.g., forming Schiff bases), while the carboxylic acid can be activated (e.g., to NHS ester) for amide bond formation. Additionally, it is utilized in surface modification of nanoparticles to improve biocompatibility and reduce immunogenicity.

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