4,4-Bis(4-hydroxyphenyl)valeric acid

98.0 %

Reagent Code: #143384
label
Alias Bisphenolate 4,4-bis(4-hydroxyphenyl)pentanoic acid
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CAS Number 126-00-1

science Other reagents with same CAS 126-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.32 g/mol
Formula C₁₇H₁₈O₄
badge Registry Numbers
EC Number 204-763-2
MDL Number MFCD00002800
thermostat Physical Properties
Melting Point 167-170 °C(lit.)
inventory_2 Storage & Handling
Density 1.30
Storage Room temperature

description Product Description

Used as a monomer in the synthesis of high-performance polymers, particularly polycarbonates and epoxy resins, due to its ability to impart thermal stability and mechanical strength. Its bulky aromatic structure enhances the glass transition temperature and improves resistance to heat and oxidation. Also explored in the development of bisphenol-free alternatives for coatings, adhesives, and engineering plastics where reduced endocrine-disrupting potential is desired. Shows potential in specialty applications requiring durability and chemical resistance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿280.00
inventory 500g
10-20 days ฿3,600.00
inventory 2.5kg
10-20 days ฿17,980.00
inventory 100g
10-20 days ฿730.00

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4,4-Bis(4-hydroxyphenyl)valeric acid
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Used as a monomer in the synthesis of high-performance polymers, particularly polycarbonates and epoxy resins, due to its ability to impart thermal stability and mechanical strength. Its bulky aromatic structure enhances the glass transition temperature and improves resistance to heat and oxidation. Also explored in the development of bisphenol-free alternatives for coatings, adhesives, and engineering plastics where reduced endocrine-disrupting potential is desired. Shows potential in specialty applicat

Used as a monomer in the synthesis of high-performance polymers, particularly polycarbonates and epoxy resins, due to its ability to impart thermal stability and mechanical strength. Its bulky aromatic structure enhances the glass transition temperature and improves resistance to heat and oxidation. Also explored in the development of bisphenol-free alternatives for coatings, adhesives, and engineering plastics where reduced endocrine-disrupting potential is desired. Shows potential in specialty applications requiring durability and chemical resistance.

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