3-hydroxytetrahydrofuran
3-furanol, tetrahydro-
Identification
| Name | 3-hydroxytetrahydrofuran |
| CAS Number | 453-20-3 |
| EINECS | 207-219-2 |
| FDA UNII | Search |
| Molecular Formula | C4 H8 O2 |
| Molecular Weight | 88.10616000 |
| MDL Number | MFCD00005374 |
| Nikkaji Number | J196.153E |
| Beilstein | 0102545 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Specific Gravity | 1.10300 to 1.10700 @ 20.00 °C. |
| Pounds per Gallon - (est). | 9.189 to 9.222 |
| Refractive Index | 1.44700 to 1.45200 @ 20.00 °C. |
| Boiling Point | 181.00 °C. @ 760.00 mm Hg |
| Vapor Pressure | 0.300000 mmHg @ 25.00 °C. (est) |
| Flash Point | 178.00 °F. TCC ( 81.11 °C. ) |
| logP (o/w) | -0.830 (est) |
| Soluble in | water, 1.00E+06 mg/L @ 25 °C (exp) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | intravenous-mouse LD50 3850 mg/kg |
| 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 3-hydroxytetrahydrofuran usage levels up to | not for fragrance use. |
| Recommendation for 3-hydroxytetrahydrofuran flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
3-
furanol, tetrahydro-
oxolan-3-ol
tetrahydro-3-furanol
PubMed:
Selective hydrodeoxygenation of cyclic vicinal diols to cyclic alcohols over tungsten oxide-palladium catalysts.
PubMed:
Step-by-step mechanism of DNA damage recognition by human 8-oxoguanine DNA glycosylase.
PubMed:
Lys98 substitution in human AP endonuclease 1 affects the kinetic mechanism of enzyme action in base excision and nucleotide incision repair pathways.
PubMed:
Electron impact ionization of furanose alcohols.
PubMed:
Alpha,gamma-cyclic peptide ensembles with a hydroxylated cavity.
PubMed:
Total dissociative electron attachment cross sections for molecular constituents of DNA.
PubMed:
Excitation, ionization, and fragmentation of chiral molecules in asymmetric microenvironments: a mass-resolved R2PI spectroscopic study.
PubMed:
Angle-resolved photoelectron spectroscopy of randomly oriented 3-hydroxytetrahydrofuran enantiomers.
PubMed:
Xylopyranoside-based agonists of D-myo-inositol 1,4,5-trisphosphate receptors: synthesis and effect of stereochemistry on biological activity.
PubMed:
Ricin A-chain inhibitors resembling the oxacarbenium ion transition state.
PubMed:
Rotational Spectroscopy and Ring-Puckering Conformation of 3-Hydroxytetrahydrofuran.
PubMed:
Simplification of adenophostin A defines a minimal structure for potent glucopyranoside-based mimics of D-myo-inositol 1,4,5-trisphosphate.
PubMed:
UV photoelectron and ab initio quantum mechanical characterization of valence electrons in Na(+)-water-2'-deoxyguanosine 5'-phosphate clusters: electronic influences on DNA alkylation by methylating and ethylating carcinogens.
PubMed:
UV photoelectron and theoretical characterization of 2'-deoxyguanosine-5'-phosphate valence electronic properties: changes in structure associated with the B to Z-DNA conformational transition.
PubMed:
Structure and conformation of pseudouridine analogues.
PubMed:
Synthesis and biological activities of ftorafur metabolites. 3'- and 4'-hydroxyftorafur.