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Home > Products >  Diphenolic acidCAS NO.: 126-00-1

Diphenolic acidCAS NO.: 126-00-1 CAS NO.126-00-1

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Keywords

  • Diphenolic acid
  • 4,4-BIS(4-HYDROXYPHENYL)-N-VALERIC ACID
  • 4,4-BIS(P-HYDROXYPHENYL)VALERIC ACID

Quick Details

  • ProName: Diphenolic acidCAS NO.: 126-00-1
  • CasNo: 126-00-1
  • Molecular Formula: C17H18O4
  • Appearance: White solid
  • Application: Adhesive and Sealant
  • DeliveryTime: in stock
  • PackAge: Aluminium foil bag
  • Port: China main port
  • ProductionCapacity: 10000 Gram/Day
  • Purity: 99%
  • Storage: Room temperature
  • Transportation: By Sea/Air/DHL
  • LimitNum: 1 Kilogram
  • first class: 1-10

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Details

Chemical Properties Light pink solid
Uses Diphenolic acid (DPA) has been identified as a potential replacement for bisphenol A, which is one of the monomers for epoxy resins and polycarbonates. DPA also can Intermediate for surface coatings, lubricating oil additives, cosmetics, surfactants, plasticizers, textile chemicals.
Preparation Diphenolic acid (DPA) can be made by the condensation reaction of levulinic acid with phenol in the presence of acid catalysts.
Synthesis of diphenolic acid from levulinic acid
Synthesis of diphenolic acid from levulinic acid
Industrial uses Diphenolic acid, the condensation product of levulinic acid and phenol, is useful in the preparation of the modified phenol formaldehyde resins, polyether resins and as monocarboxilic acid chain stopper in alkyd resin (Bader, 1960). Further, diphenolic acid can be substituted for bis-phenol A, the primary raw material for production of epoxy resin.
Purification Methods When recrystallised from *C6H6, the crystals have 0.5 mol of *C6H6 (m 120-122o), and when recrystallised from toluene, the crystals have 0.5 mol of toluene. Purify the acid by recrystallisation from hot H2O. It is soluble in Me2CO, AcOH, EtOH, propan-2-ol, methyl ethyl ketone. It can also be recrystallised from AcOH, heptane/Et2O or Me2CO/*C6H6. It has max 225 and 279nm in EtOH. The methyl ester has m 87-89o (aqueous MeOH to give the trihydrate). [Bader & Kantowicz J Am Chem Soc 76 4465 1954, Beilstein 10 IV 1890.]

 

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