2,5-Dimethylfuran (English Wikipedia)

Patrick L. Brezonik. Chemical Kinetics and Process Dynamics in Aquatic Systems. CRC Press, 1994, p. 671. [1] Archived 2020-07-24 at the Wayback Machine
Peter Arlien-Søborg. Solvent Neurotoxicity. CRC Press, 1992. ISBN 0-8493-6234-2. [2] Archived 2021-02-21 at the Wayback Machine
Donald Shopland. Cigars: Health Effects and Trends. DIANE Publishing, 1998. [3] Archived 2020-07-24 at the Wayback Machine

chemexper.com

"ChemExper chemical directory - Catalog of chemicals and suppliers". Archived from the original on 2011-09-27. Retrieved 2011-03-17.

chemicalbook.com

"2,5-Dimethylfuran(625-86-5)". Chemical Book. Archived from the original on 2017-05-04. Retrieved 2017-07-21.

doi.org

Yuriy Román-Leshkov; Christopher J. Barrett; Zhen Y. Liu; James A. Dumesic (2007). "Production of dimethylfuran for liquid fuels from biomass-derived carbohydrates". Nature. 447 (7147): 982–5. Bibcode:2007Natur.447..982R. doi:10.1038/nature05923. PMID 17581580. S2CID 4366510.
Haibo Zhao; Johnathan E. Holladay; Heather Brown; Z. Conrad Zhang (June 15, 2007). "Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural". Science. 316 (5831): 1597–1600. Bibcode:2007Sci...316.1597Z. doi:10.1126/science.1141199. PMID 17569858. S2CID 39295324.
S. W. Gerritz; A. M. Sefler (2000). "2,5-Dimethylfuran (DMFu): An Internal Standard for the "Traceless" Quantitation of Unknown Samples via 1H NMR". J. Comb. Chem. 2 (1): 39–41. doi:10.1021/cc990041v. PMID 10813883.
W.D. Powrie; C.H. Wu; V.P. Molund (1986). "Browning reaction systems as sources of mutagens and antimutagens". Environmental Health Perspectives. 67: 47–54. doi:10.2307/3430317. JSTOR 3430317. PMC 1474410. PMID 3757959.
Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.

ecofriendlymag.com

"Direct-Injection Engine Study Finds That DMF Is a Promising Biofuel, With Combustion Performance and Regulated Emissions Comparable to Gasoline | Eco Friendly". Archived from the original on 2013-01-21.

equivashellmsds.com

"Equiva Services - MSDS". Archived from the original on 2011-07-10.

fishersci.com

"Safety Data Sheet: 2,5-Dimethylfuran". Thermo Fisher Scientific. Archived from the original on 2014-03-07. Retrieved 2014-03-07.

greencarcongress.com

"Green Car Congress: Direct-Injection Engine Study Finds That DMF Is a Promising Biofuel, With Combustion Performance and Regulated Emissions Comparable to Gasoline". Archived from the original on 2011-12-24. Retrieved 2011-03-17.

harvard.edu

ui.adsabs.harvard.edu

Yuriy Román-Leshkov; Christopher J. Barrett; Zhen Y. Liu; James A. Dumesic (2007). "Production of dimethylfuran for liquid fuels from biomass-derived carbohydrates". Nature. 447 (7147): 982–5. Bibcode:2007Natur.447..982R. doi:10.1038/nature05923. PMID 17581580. S2CID 4366510.
Haibo Zhao; Johnathan E. Holladay; Heather Brown; Z. Conrad Zhang (June 15, 2007). "Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural". Science. 316 (5831): 1597–1600. Bibcode:2007Sci...316.1597Z. doi:10.1126/science.1141199. PMID 17569858. S2CID 39295324.
Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.

jstor.org

W.D. Powrie; C.H. Wu; V.P. Molund (1986). "Browning reaction systems as sources of mutagens and antimutagens". Environmental Health Perspectives. 67: 47–54. doi:10.2307/3430317. JSTOR 3430317. PMC 1474410. PMID 3757959.

nih.gov

pubmed.ncbi.nlm.nih.gov

Yuriy Román-Leshkov; Christopher J. Barrett; Zhen Y. Liu; James A. Dumesic (2007). "Production of dimethylfuran for liquid fuels from biomass-derived carbohydrates". Nature. 447 (7147): 982–5. Bibcode:2007Natur.447..982R. doi:10.1038/nature05923. PMID 17581580. S2CID 4366510.
Haibo Zhao; Johnathan E. Holladay; Heather Brown; Z. Conrad Zhang (June 15, 2007). "Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural". Science. 316 (5831): 1597–1600. Bibcode:2007Sci...316.1597Z. doi:10.1126/science.1141199. PMID 17569858. S2CID 39295324.
S. W. Gerritz; A. M. Sefler (2000). "2,5-Dimethylfuran (DMFu): An Internal Standard for the "Traceless" Quantitation of Unknown Samples via 1H NMR". J. Comb. Chem. 2 (1): 39–41. doi:10.1021/cc990041v. PMID 10813883.
W.D. Powrie; C.H. Wu; V.P. Molund (1986). "Browning reaction systems as sources of mutagens and antimutagens". Environmental Health Perspectives. 67: 47–54. doi:10.2307/3430317. JSTOR 3430317. PMC 1474410. PMID 3757959.
Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.

ncbi.nlm.nih.gov

W.D. Powrie; C.H. Wu; V.P. Molund (1986). "Browning reaction systems as sources of mutagens and antimutagens". Environmental Health Perspectives. 67: 47–54. doi:10.2307/3430317. JSTOR 3430317. PMC 1474410. PMID 3757959.

pnl.gov

"Plastic that grows on trees". Pacific Northwest National Laboratory. 2007-06-21. Archived from the original (press release) on 13 July 2007. Retrieved 2007-06-22.

semanticscholar.org

api.semanticscholar.org

Yuriy Román-Leshkov; Christopher J. Barrett; Zhen Y. Liu; James A. Dumesic (2007). "Production of dimethylfuran for liquid fuels from biomass-derived carbohydrates". Nature. 447 (7147): 982–5. Bibcode:2007Natur.447..982R. doi:10.1038/nature05923. PMID 17581580. S2CID 4366510.
Haibo Zhao; Johnathan E. Holladay; Heather Brown; Z. Conrad Zhang (June 15, 2007). "Metal Chlorides in Ionic Liquid Solvents Convert Sugars to 5-Hydroxymethylfurfural". Science. 316 (5831): 1597–1600. Bibcode:2007Sci...316.1597Z. doi:10.1126/science.1141199. PMID 17569858. S2CID 39295324.
Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.

t3db.ca

"Material Safety Data Sheet 2,5-Dimethylfuran" (PDF). 6 January 2012. Archived (PDF) from the original on 4 August 2022.

web.archive.org

"ChemExper chemical directory - Catalog of chemicals and suppliers". Archived from the original on 2011-09-27. Retrieved 2011-03-17.
Matt McGrath (2007-06-21). "Fruit could make 'powerful fuel'". BBC News. Archived from the original on 2007-08-17. Retrieved 2007-06-22.
"Plastic that grows on trees". Pacific Northwest National Laboratory. 2007-06-21. Archived from the original (press release) on 13 July 2007. Retrieved 2007-06-22.
James Beal (2007-06-20). "Engineers develop higher-energy liquid-transportation fuel from sugar" (press release). University of Wisconsin-Madison. Archived from the original on 1 July 2007. Retrieved 2007-06-22.
"Green Car Congress: Direct-Injection Engine Study Finds That DMF Is a Promising Biofuel, With Combustion Performance and Regulated Emissions Comparable to Gasoline". Archived from the original on 2011-12-24. Retrieved 2011-03-17.
Patrick L. Brezonik. Chemical Kinetics and Process Dynamics in Aquatic Systems. CRC Press, 1994, p. 671. [1] Archived 2020-07-24 at the Wayback Machine
Peter Arlien-Søborg. Solvent Neurotoxicity. CRC Press, 1992. ISBN 0-8493-6234-2. [2] Archived 2021-02-21 at the Wayback Machine
Donald Shopland. Cigars: Health Effects and Trends. DIANE Publishing, 1998. [3] Archived 2020-07-24 at the Wayback Machine
Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.
"Safety Data Sheet: 2,5-Dimethylfuran". Thermo Fisher Scientific. Archived from the original on 2014-03-07. Retrieved 2014-03-07.
"2,5-Dimethylfuran(625-86-5)". Chemical Book. Archived from the original on 2017-05-04. Retrieved 2017-07-21.
"Material Safety Data Sheet 2,5-Dimethylfuran" (PDF). 6 January 2012. Archived (PDF) from the original on 4 August 2022.
"Equiva Services - MSDS". Archived from the original on 2011-07-10.
"hazard.com". Archived from the original on 2011-07-11. Retrieved 2010-12-27.{{cite web}}: CS1 maint: unfit URL (link)
"hazard.com". Archived from the original on 2011-07-11. Retrieved 2010-12-27.{{cite web}}: CS1 maint: unfit URL (link)

wisc.edu

news.wisc.edu

James Beal (2007-06-20). "Engineers develop higher-energy liquid-transportation fuel from sugar" (press release). University of Wisconsin-Madison. Archived from the original on 1 July 2007. Retrieved 2007-06-22.

zenodo.org

Ashley, D. L.; Bonin, M. A.; Hamar, B.; McGeehin, M. (1996). "Using the blood concentration of 2,5-dimethylfuran as a marker for smoking". International Archives of Occupational and Environmental Health. 68 (3): 183–7. Bibcode:1996IAOEH..68..183A. doi:10.1007/BF00381629. PMID 8919847. S2CID 22233967. Archived from the original on 2021-02-21. Retrieved 2020-09-12.