3238-40-2

  • Product Name:2,5-Furandicarboxylic acid
  • Molecular Formula:C6H4O5
  • Purity:99%
  • Molecular Weight:156.095
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Product Details;

CasNo: 3238-40-2

Molecular Formula: C6H4O5

Appearance: White powder

factory and supplier 3238-40-2 2,5-Furandicarboxylic acid in stock

  • Molecular Formula:C6H4O5
  • Molecular Weight:156.095
  • Appearance/Colour:White powder 
  • Vapor Pressure:8.9E-08mmHg at 25°C 
  • Melting Point:>310°C (dec.) 
  • Refractive Index:1.58 
  • Boiling Point:419.2 °C at 760 mmHg 
  • PKA:2.28±0.10(Predicted) 
  • Flash Point:207.3 °C 
  • PSA:87.74000 
  • Density:1.604 g/cm3 
  • LogP:0.67600 

2,5-Furandicarboxylic acid(Cas 3238-40-2) Usage

Preparation

2,5-Furandicarboxylic acid (FDCA) can be produced from biomass or its derived sugars or platform chemicals, and has demonstrated to be a very promising substitute for petroleum-derived polymer products.Chapter 5 - Advances in the synthesis and application of 2,5-furandicarboxylic acid

Synthesis Reference(s)

Tetrahedron Letters, 26, p. 1777, 1985 DOI: 10.1016/S0040-4039(00)98336-9

Flammability and Explosibility

Notclassified

Solubility in organics

2,5-Furandicarboxylic acid (FDCA) serves as a monomer in various polyesters and is often obtained through the oxidation of 5-hydroxymethylfurfural. In pure solvents and binary mixtures, the solubility of FDCA increased with the increasing temperature. The order from largest to smallest solubility in pure solvents was as follows: methanol, 1-butanol, isobutanol, acetic acid, water, MIBK, ethyl acetate, and acetonitrile.https://doi.org/10.1021/acs.jced.7b00927

Definition

ChEBI: A member of the class of furans carrying two carboxy substituents at positions 2 and 5.

Application

2,5-Furandicarboxylic acid (FDCA) is a renewable, greener substitute for terephthalate in the production of polyesters. It is widely used as a precursor for the synthesis of bio-based polyesters and various other polymers.Applications of FDCA in the synthesis of several metal-organic frameworks (MOFs) have also been reported.

InChI:InChI=1/C6H4O5/c7-5(8)3-1-2-4(11-3)6(9)10/h1-2H,(H,7,8)(H,9,10)

3238-40-2 Relevant articles

Tunable mixed oxides based on CeO2 for the selective aerobic oxidation of 5-(hydroxymethyl)furfural to FDCA in water

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A one pot-two step procedure for the syn...

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The development of efficient encapsulati...

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The catalytic promiscuity of hemoglobin ...

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Mixed noblility: We show that the modifi...

Selective Aerobic Oxidation of 5-(Hydroxymethyl)furfural over Heterogeneous Silver-Gold Nanoparticle Catalysts

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Supported gold- and silver-based catalysts for the selective aerobic oxidation of 5-(hydroxymethyl)furfural to 2,5-furandicarboxylic acid and 5-hydroxymethyl-2-furancarboxylic acid

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Efficient synthesis of 2,5-furandicarboxylic acid from biomass-derived 5-hydroxymethylfurfural in 1,4-dioxane/H2O mixture

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Electrocatalytic conversion of biomass-d...

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Herein, a one-dimensional hollow nanofib...

3238-40-2 Process route

bromine
7726-95-6

bromine

cis-2H,5H-dihydrofuran-2,5-dicarboxylic acid
2043-98-3

cis-2H,5H-dihydrofuran-2,5-dicarboxylic acid

furan-2,5-dicarboxylic acid
3238-40-2

furan-2,5-dicarboxylic acid

hydrogen bromide
10035-10-6,12258-64-9

hydrogen bromide

Conditions
Conditions Yield
at 140 ℃; im geschlossenen Rohr;
potassium furan-2-carboxylate
20842-02-8

potassium furan-2-carboxylate

furan-2,5-dicarboxylic acid
3238-40-2

furan-2,5-dicarboxylic acid

2,4-furan dicarboxylic acid
4282-28-4

2,4-furan dicarboxylic acid

Conditions
Conditions Yield
With cadmium(II) iodide; at 265 ℃; for 4h; Reagent/catalyst; Temperature; Overall yield = 89 %; Inert atmosphere; Dean-Stark; Cooling with acetone-dry ice;
60.9%

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    5-hydroxymethyl-2-furfuraldehyde

3238-40-2 Downstream products

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    15719-64-9

    methylammonium carbonate

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