EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

3-hydroxytetrahydrofuran
3-furanol, tetrahydro-

Supplier Sponsors

CAS Number: 453-20-3Picture of molecule3D/inchi
Other(deleted CASRN):84921-89-1
ECHA EINECS - REACH Pre-Reg:207-219-2
FDA UNII: Search
Nikkaji Web:J196.153E
Beilstein Number:0102545
MDL:MFCD00005374
XlogP3-AA:-0.40 (est)
Molecular Weight:88.10616000
Formula:C4 H8 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
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)
 water, 1e+006 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
3-Hydroxytetrahydrofuran 97.0%
Matrix Scientific
For experimental / research use only.
3-Hydroxytetrahydrofuran, >95%
sds
Santa Cruz Biotechnology
For experimental / research use only.
3-Hydroxytetrahydrofuran
Sigma-Aldrich: Aldrich
For experimental / research use only.
3-Hydroxytetrahydrofuran ReagentPlus®, 98%
sds
TCI AMERICA
For experimental / research use only.
3-Hydroxytetrahydrofuran >97.0%(GC)
sds
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intravenous-mouse LD50 3850 mg/kg
BEHAVIORAL: ATAXIA BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Journal of Pharmacy and Pharmacology. Vol. 22, Pg. 694, 1970.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
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.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):453-20-3
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :9960
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
oxolan-3-ol
Chemidplus:0000453203
RTECS:LU3450050 for cas# 453-20-3
 
References:
 oxolan-3-ol
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):9960
Pubchem (sid):134975487
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2932.19.5000
ChemSpider:View
Wikipedia:View
EFSA Update of results on the monitoring of furan levels in food:Read Report
EFSA Previous report: Results on the monitoring of furan levels in food:Read Report
EFSA Report of the CONTAM Panel on provisional findings on furan in food:Read Report
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
3-furanol, tetrahydro-
 oxolan-3-ol
 tetrahydro-3-furanol
 

Articles:

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.
 
Notes:
None found
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