2,5-furan dimethanol
[5-(hydroxymethyl)-2-furyl]methan-1-ol
Identification
| Name | 2,5-furan dimethanol |
| IUPAC | [5-(hydroxymethyl)furan-2-yl]methanol |
| CAS Number | 1883-75-6 |
| EINECS | 217-544-1 |
| FDA UNII | Search |
| Molecular Formula | C6 H8 O3 |
| Molecular Weight | 128.12736000 |
| MDL Number | MFCD00003253 |
| Nikkaji Number | J199.705J |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 275.00 to 276.00 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.002000 mmHg @ 25.00 °C. (est) |
| Flash Point | 249.00 °F. TCC ( 120.30 °C. ) (est) |
| logP (o/w) | -1.326 (est) |
| Soluble in | alcohol |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | information only not used for fragrances or flavors |
| Recommendation for 2,5-furan dimethanol usage levels up to | not for fragrance use. |
| Recommendation for 2,5-furan dimethanol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2,5-
dihydroxymethylfuran
furan-2,5-diyldimethanol
2,5-
furandimethanol
furfuryl alcohol, 5-hydroxymethyl-
(5-
hydroxymethyl-furan-2-yl)-methanol
[5-(
hydroxymethyl)-2-furyl]methan-1-ol
2,5-bis(
hydroxymethyl)furan
[5-(
hydroxymethyl)furan-2-yl]methanol
5-(
hydroxymethyl)furfuryl alcohol
PubMed:
Tunable and Selective Conversion of 5-HMF to 2,5-Furandimethanol and 2,5-Dimethylfuran over Copper-Doped Porous Metal Oxides.
PubMed:
Enzymatic synthesis of biobased polyesters using 2,5-bis(hydroxymethyl)furan as the building block.
PubMed:
Biphasic catalytic conversion of fructose by continuous hydrogenation of HMF over a hydrophobic ruthenium catalyst.
PubMed:
[Effect of acetic acid, furfural and 5-hydroxymethylfurfural on production of 2,3-butanediol by Klebsiella oxytoca].
PubMed:
Toxic hazard and chemical analysis of leachates from furfurylated wood.
PubMed:
Furan oligomers and beta-carbolines from terrestrial streptomycetes.
PubMed:
Adaptive response of yeasts to furfural and 5-hydroxymethylfurfural and new chemical evidence for HMF conversion to 2,5-bis-hydroxymethylfuran.
PubMed:
Xylaramide, a new antifungal compound, and other secondary metabolites from Xylaria longipes.
PubMed:
Some prevalent biomolecules as defenses against singlet oxygen damage.