4-((2-((4-((2-Hydroxyethoxy)carbonyl)benzoyl)oxy)ethoxy)carbonyl)benzoic acid

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Reagent Code: #131226
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CAS Number 23186-89-2

science Other reagents with same CAS 23186-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.35 g/mol
Formula C₂₀H₁₈O₉
thermostat Physical Properties
Boiling Point 628.3±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.384±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pH-sensitive and enzyme-responsive prodrugs, particularly in targeted drug delivery systems. Its carboxyl and hydroxyl functional groups allow for easy conjugation with active pharmaceutical ingredients, enabling controlled release in specific physiological environments. Commonly employed in the development of polymer-drug conjugates and biodegradable hydrogels for cancer therapy and anti-inflammatory treatments. Also utilized in the preparation of stimuli-responsive nanocarriers that degrade under acidic conditions, such as those found in tumor tissues or intracellular endosomes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿25,600.00
inventory 250mg
10-20 days ฿81,200.00

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4-((2-((4-((2-Hydroxyethoxy)carbonyl)benzoyl)oxy)ethoxy)carbonyl)benzoic acid
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Used as a key intermediate in the synthesis of pH-sensitive and enzyme-responsive prodrugs, particularly in targeted drug delivery systems. Its carboxyl and hydroxyl functional groups allow for easy conjugation with active pharmaceutical ingredients, enabling controlled release in specific physiological environments. Commonly employed in the development of polymer-drug conjugates and biodegradable hydrogels for cancer therapy and anti-inflammatory treatments. Also utilized in the preparation of stimuli-r

Used as a key intermediate in the synthesis of pH-sensitive and enzyme-responsive prodrugs, particularly in targeted drug delivery systems. Its carboxyl and hydroxyl functional groups allow for easy conjugation with active pharmaceutical ingredients, enabling controlled release in specific physiological environments. Commonly employed in the development of polymer-drug conjugates and biodegradable hydrogels for cancer therapy and anti-inflammatory treatments. Also utilized in the preparation of stimuli-responsive nanocarriers that degrade under acidic conditions, such as those found in tumor tissues or intracellular endosomes.

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