Furfurylalcoholresin
Product Information
Molecular Formula
C5H6O2||||C5H6O2||||C5H6O2
Molecular Weight
98.10
Description
Dark. viscous. fluid with double bonds in the polymer backbone.
Synonyms
furfuryl alcohol; 2-Furanmethanol; furan-2-ylmethanol; 2-Furylmethanol; 2-Furancarbinol; 2-Furylcarbinol; Furfural alcohol; 2-Furanylmethanol; Furfuranol; 2-Furfuryl alcohol; Furfuralcohol; Furfurylalcohol; 2-(Hydroxymethyl)furan; 5-Hydroxymethylfuran; Furyl alcohol; 2-Hydroxymethylfuran; alpha-Furylcarbinol; Furylcarbinol; Furfurol; Furan-2-yl-methanol; 2-Furfurylalkohol; Furfurylcarb; Methanol, (2-furyl)-; (2-furyl)methanol; 2-hydroxymethylfurane; Furylcarbinol (VAN); Furan-2-methanol; 2-Furane-methanol; (furan-2-yl)methanol; 2-furanemethanol; Qo furfuryl alcohol; alpha-Furylcarbinol
IUPAC Name
furan-2-ylmethanol
SMILES
C1=COC(=C1)CO
InChI
InChI=1S/C5H6O2/c6-4-5-2-1-3-7-5/h1-3,6H,4H2
InChI Key
XPFVYQJUAUNWIW-UHFFFAOYSA-N
Boiling Point
338 °F at 760 mmHg
Melting Point
-24 °F
Flash Point
167 °F
Density
1.13 at 68 °F
Solubility
greater than or equal to 100 mg/mL at 73 °F
Appearance
Colorless to yellow liquid
Application
Used as a solvent and as an intermediate in the manufacturing of resins and wetting agents; Used as a solvent for tanning agents, dyes, and resins; also used in sealants, cements, and furan and urea-formaldehyde polymers; The most important use is in making poly(furfuryl alcohol) resins to bind sand-based cores and molds in foundries and to produce plastics, cements, mortars, binders, and adhesives. Resins made from furfuryl alcohol are chemical-resistant and nonburning.
Storage
Store at room temperature
Refractive Index
n20/D 1.36
Viscosity
14.500±2500 cps
Stability
Turns amber due to autoxidation and intermolecular dehydration during storage and turns black in presence of air
LogP
log Kow= 0.28
Vapor Pressure
0.4 mmHg at 68 °F
Henry's Law Constant
7.9X10-8 atm cu m/mol at 25 °C (est)
Dissociation Constants
pKa = 9.55
Odor
Faint burning odor
Safety Information
Hazards
Irritant
Handling
Glove. chemical goggles & fume hood
Computed Properties
XLogP3
0.3
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
1
Exact Mass
98.036779430 g/mol
Monoisotopic Mass
98.036779430 g/mol
Topological Polar Surface Area
33.4Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
54
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-114163593-A | Polyether modified phenolic resin for heavy-load grinding wheel and preparation method thereof | 2022-02-15 |
| CN-114094109-A | Lithium ion battery | 2022-01-19 |
| CN-114068936-A | Lithium ion battery | 2022-01-14 |
| CN-114044509-A | Preparation method of ordered microporous carbon with precise pore diameter | 2021-12-28 |
| CN-114106510-A | Production process of environment-friendly phenol urea formaldehyde modified furan resin | 2021-12-22 |
| CN-114133368-A | Method for extracting ethyl maltol from maltol chlorination hydrolysate by direct sublimation | 2021-12-20 |
| CN-114132042-A | Production process of micro-solid plate | 2021-12-18 |
| CN-114058305-A | Novel insulating, heat-insulating and anti-seismic sealant and preparation method thereof | 2021-12-17 |
| CN-113980225-A | Hydroxypropyl distarch phosphate modified waterborne polyurethane resin and preparation method thereof | 2021-12-09 |
| CN-114100691-A | Glycosyl mesoporous zirconium-containing composite material and preparation method and application thereof | 2021-12-08 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 29908303 | 2018-10-01 | Hemoglobin adducts of furfuryl alcohol in genetically modified mouse models: Role of endogenous sulfotransferases 1a1 and 1d1 and transgenic human sulfotransferases 1A1/1A2 | Toxicology letters |
| 25370010 | 2016-01-01 | Bioactivation of food genotoxicants 5-hydroxymethylfurfural and furfuryl alcohol by sulfotransferases from human, mouse and rat: a comparative study | Archives of toxicology |
| 25053625 | 2014-10-01 | The effect of knockout of sulfotransferases 1a1 and 1d1 and of transgenic human sulfotransferases 1A1/1A2 on the formation of DNA adducts from furfuryl alcohol in mouse models | Carcinogenesis |
| 22953863 | 2012-12-01 | Quantification of furanic compounds in coated deep-fried products simulating normal preparation and consumption: optimisation of HS-SPME analytical conditions by response surface methodology | Food chemistry |
| 22938198 | 2012-10-10 | High structure sensitivity of vapor-phase furfural decarbonylation/hydrogenation reaction network as a function of size and shape of Pt nanoparticles | Nano letters |
| 23107675 | 2012-09-15 | Characterisation of bound volatile compounds of a low flavour kiwifruit species: Actinidia eriantha | Food chemistry |
| 22829466 | 2012-09-03 | Control of porosity by using isoreticular zeolitic imidazolate frameworks (IRZIFs) as a template for porous carbon synthesis | Chemistry (Weinheim an der Bergstrasse, Germany) |
| 22648683 | 2012-09-01 | In vivo detoxification of furfural during lipid production by the oleaginous yeast Trichosporon fermentans | Biotechnology letters |
| 22785445 | 2012-09-01 | Characterization of the polymerization of furfuryl alcohol during roasting of coffee | Food & function |
| 22871058 | 2012-08-29 | Furfuraldehyde hydrogenation on titanium oxide-supported platinum nanoparticles studied by sum frequency generation vibrational spectroscopy: acid-base catalysis explains the molecular origin of strong metal-support interactions | Journal of the American Chemical Society |
