4-[2-[2-(3-Sulfanylpropanoylamino)ethoxy]ethoxy]butanoic acid

M.w.3000

Reagent Code: #237880
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CAS Number 1220112-75-3

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.36 g/mol
Formula C₁₁H₂₁NO₅S
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of peptide-based pharmaceuticals and bioconjugates due to its bifunctional structure containing both carboxylic acid and thiol-reactive amide groups. The molecule enables controlled linker formation between biomolecules and functional payloads, such as drugs, dyes, or detection tags, especially in targeted therapies and diagnostic reagents. Its hydrophilic ethoxy spacers enhance solubility in aqueous systems, making it suitable for bioconjugation under physiological conditions. Also applied in the development of PEG-like linkers with improved metabolic stability and reduced immunogenicity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,190.00
4-[2-[2-(3-Sulfanylpropanoylamino)ethoxy]ethoxy]butanoic acid
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Used as a key intermediate in the synthesis of peptide-based pharmaceuticals and bioconjugates due to its bifunctional structure containing both carboxylic acid and thiol-reactive amide groups. The molecule enables controlled linker formation between biomolecules and functional payloads, such as drugs, dyes, or detection tags, especially in targeted therapies and diagnostic reagents. Its hydrophilic ethoxy spacers enhance solubility in aqueous systems, making it suitable for bioconjugation under physiolo

Used as a key intermediate in the synthesis of peptide-based pharmaceuticals and bioconjugates due to its bifunctional structure containing both carboxylic acid and thiol-reactive amide groups. The molecule enables controlled linker formation between biomolecules and functional payloads, such as drugs, dyes, or detection tags, especially in targeted therapies and diagnostic reagents. Its hydrophilic ethoxy spacers enhance solubility in aqueous systems, making it suitable for bioconjugation under physiological conditions. Also applied in the development of PEG-like linkers with improved metabolic stability and reduced immunogenicity.

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