4-(4-Hydroxybutoxy)-4-oxobutanoic acid

95%

Reagent Code: #131493
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CAS Number 56149-52-1

science Other reagents with same CAS 56149-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.19 g/mol
Formula C₈H₁₄O₅
badge Registry Numbers
MDL Number MFCD00517728
thermostat Physical Properties
Boiling Point 373.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.217±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of biodegradable polymers and functionalized esters, particularly in the production of polyesters and polyurethanes with tailored degradation profiles. Its bifunctional structure, featuring both carboxylic acid and hydroxyl groups, enables cross-linking and copolymerization, making it valuable in developing environmentally friendly coatings, drug delivery systems, and tissue engineering scaffolds. Also employed in modifying surface properties of biomaterials due to its ability to introduce hydrophilic spacers in molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,960.00
inventory 250mg
10-20 days ฿13,620.00
inventory 1g
10-20 days ฿44,800.00

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4-(4-Hydroxybutoxy)-4-oxobutanoic acid
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Used as an intermediate in the synthesis of biodegradable polymers and functionalized esters, particularly in the production of polyesters and polyurethanes with tailored degradation profiles. Its bifunctional structure, featuring both carboxylic acid and hydroxyl groups, enables cross-linking and copolymerization, making it valuable in developing environmentally friendly coatings, drug delivery systems, and tissue engineering scaffolds. Also employed in modifying surface properties of biomaterials due t

Used as an intermediate in the synthesis of biodegradable polymers and functionalized esters, particularly in the production of polyesters and polyurethanes with tailored degradation profiles. Its bifunctional structure, featuring both carboxylic acid and hydroxyl groups, enables cross-linking and copolymerization, making it valuable in developing environmentally friendly coatings, drug delivery systems, and tissue engineering scaffolds. Also employed in modifying surface properties of biomaterials due to its ability to introduce hydrophilic spacers in molecular architectures.

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