Bio-based platform chemical (aldehyde derived from lignocellulosic biomass)
[2]
Key properties
Oxygen-rich furanic aldehyde
Derived from hemicellulose (xylose dehydration)
Highly reactive in C–C coupling reactions
Prone to polymerisation (humin formation) in aqueous/acidic environments
[1]
Contains reactive aldehyde (–CHO) group
Derived from renewable biomass
Limited direct polymerizability (low ceiling temperature)
Can undergo cationic copolymerization
Precursor to furan-based chemicals
[2]
Platform molecule for biofuels and biochemicals
Precursor for sustainable aviation fuel (SAF) intermediates
Substrate for aldol condensation reactions
[1]
Intermediate for biofuels and solvents
Monomer (after modification or copolymerization)
Building block for sustainable polymers
[2]
Classification by use
Chemicals used as biomass-derived platform chemicals
Chemicals used in sustainable aviation fuel production
Chemicals used in C–C coupling reactions
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[Cite:1] Light or acid? Suppressing water deactivation in SAF production via phenyl-mediated charge transfer in WOx/ZrOx-functionalised PMOs, Applied Catalysis O: Open, Volume 209, December 2025, 207078
[Cite:2] Cationic copolymerization of furfural and furfural-derived 3,4-dihydropyran: biobased and biodegradable polyacetals with high glass transition temperatures, European Polymer Journal, Volume 242, 22 January 2026, 114454