Acetonitrilo (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acetonitrilo" in Galician language version.

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9doi.org

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archive.org

Karakida, Ken'ichi; Fukuyama, Tsutomu; Kuchitsu, Kozo (1974). "Molecular Structures of Hydrogen Cyanide and Acetonitrile as Studied by Gas Electron Diffraction". Bulletin of the Chemical Society of Japan 47 (2): 299–304. doi:10.1246/bcsj.47.299.
Cramer, R. E.; Bopp, T. T. (1977). "Graphical display of the enthalpies of adduct formation for Lewis acids and bases". Journal of Chemical Education 54: 612–613. doi:10.1021/ed054p612. Os gráficos mostrados neste artigo utilizan os parámetros vellos. Os parámetros E&C mellorados están listados no modelo ECW.

books.google.com

Dumas, J.-B. (1847). "Action de l'acide phosphorique anhydre sur les sels ammoniacaux" [Action of anhydrous phosphoric acid on ammonium salts]. Comptes rendus 25: 383–384.

doi.org

dx.doi.org

Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 902. ISBN 978-0-85404-182-4. doi:10.1039/9781849733069-FP001.
Karakida, Ken'ichi; Fukuyama, Tsutomu; Kuchitsu, Kozo (1974). "Molecular Structures of Hydrogen Cyanide and Acetonitrile as Studied by Gas Electron Diffraction". Bulletin of the Chemical Society of Japan 47 (2): 299–304. doi:10.1246/bcsj.47.299.
Rhimi, B.; Mhamdi, M.; Ghorbel, A.; Narayana Kalevaru, V.; Martin, A.; Perez-Cadenas, M.; Guerrero-Ruiz, A. (15 May 2016). "Ammoxidation of ethylene to acetonitrile over vanadium and molybdenum supported zeolite catalysts prepared by solid-state ion exchange". Journal of Molecular Catalysis A: Chemical 416: 127–139. doi:10.1016/j.molcata.2016.02.028.
A. Tullo (2008). "A Solvent Dries Up". Chemical & Engineering News 86 (47): 27. doi:10.1021/cen-v086n047.p027.
Caravati, E. M.; Litovitz, T. (1988). "Pediatric cyanide intoxication and death from an acetonitrile-containing cosmetic". J. Am. Med. Assoc. 260 (23): 3470–73. PMID 3062198. doi:10.1001/jama.260.23.3470.
Ahmed, A. E.; Farooqui, M. Y. H. (1982). "Comparative toxicities of aliphatic nitriles". Toxicol. Lett. 12 (2–3): 157–64. PMID 6287676. doi:10.1016/0378-4274(82)90179-5.
Pozzani, U. C.; Carpenter, C. P.; Palm, P. E.; Weil, C. S.; Nair, J. H. (1959). "An investigation of the mammalian toxicity of acetonitrile". J. Occup. Med. 1 (12): 634–642. PMID 14434606. doi:10.1097/00043764-195912000-00003.
Cramer, R. E.; Bopp, T. T. (1977). "Graphical display of the enthalpies of adduct formation for Lewis acids and bases". Journal of Chemical Education 54: 612–613. doi:10.1021/ed054p612. Os gráficos mostrados neste artigo utilizan os parámetros vellos. Os parámetros E&C mellorados están listados no modelo ECW.
Haiges, Ralf; Baxter, Amanda F.; Goetz, Nadine R.; Axhausen, Joachim A.; Soltner, Theresa; Kornath, Andreas; Christe, Kalr O. "Protonation of nitriles: isolation and characterization of alkyl- and arylnitrilium ions". doi:10.1039/C6DT01301E.

epa.gov

Greenberg, Mark (1999). Toxicological Review of Acetonitrile (PDF). Washington, DC: U.S. Environmental Protection Agency.

espacenet.com

worldwide.espacenet.com

Patente US 4179462 Arquivado 05 de abril de 2022 en Wayback Machine., Olive, G. & Olive, S., "Process for preparing acetonitrile", published 1979-12-18, assigned to Monsanto Company

europa.eu

eur-lex.europa.eu

"Twenty-Fifth Commission Directive 2000/11/EC of 10 March 2000 adapting to technical progress Annex II to Council Directive 76/768/EEC on the approximation of laws of the Member States relating to cosmetic products". Official Journal of the European Communities L65: 22–25. 2000-03-14. Arquivado dende o orixinal o 30 de maio de 2013. Consultado o 30 de agosto de 2020.

hdinresearch.com

News. Company news. Acetonitrile Market: Global Production Capacity will reach to 271,800 Tons in 2019.

inchem.org

International Programme on Chemical Safety (1993). "Environmental Health Criteria 154. Acetonitrile". Geneva: World Health Organization.

industrialchemistry.info

"Archived copy" (PDF). Ashford's Dictionary of Industrial Chemicals, Third edition. p. 76. Arquivado dende o orixinal (PDF) o 16 de maio de 2011. Consultado o 2011-03-31.

inrs.fr

Institut national de recherche et de sécurité (INRS) (2004). Fiche toxicologique no. 104 : Acétonitrile (PDF). Paris: INRS. ISBN 2-7389-1278-8. Arquivado dende o orixinal (PDF) o 28 de xullo de 2011. Consultado o 2008-08-19.

jrc.it

ecb.jrc.it

Spanish Ministry of Health (2002). Acetonitrile. Summary Risk Assessment Report (PDF). Ispra (VA), Italy: European Chemicals Bureau. Special Publication I.01.65. Arquivado dende o orixinal (PDF) o 17 de decembro de 2008. Consultado o 30 de agosto de 2020.

nih.gov

ncbi.nlm.nih.gov

Caravati, E. M.; Litovitz, T. (1988). "Pediatric cyanide intoxication and death from an acetonitrile-containing cosmetic". J. Am. Med. Assoc. 260 (23): 3470–73. PMID 3062198. doi:10.1001/jama.260.23.3470.
Ahmed, A. E.; Farooqui, M. Y. H. (1982). "Comparative toxicities of aliphatic nitriles". Toxicol. Lett. 12 (2–3): 157–64. PMID 6287676. doi:10.1016/0378-4274(82)90179-5.
Pozzani, U. C.; Carpenter, C. P.; Palm, P. E.; Weil, C. S.; Nair, J. H. (1959). "An investigation of the mammalian toxicity of acetonitrile". J. Occup. Med. 1 (12): 634–642. PMID 14434606. doi:10.1097/00043764-195912000-00003.

orgsyn.org

DiBiase, S. A.; Beadle, J. R.; Gokel, G. W. "Synthesis of α,β-Unsaturated Nitriles from Acetonitrile: Cyclohexylideneacetonitrile and Cinnamonitrile". Org. Synth. cv7p0108.

sciencedirect.com

Steiner, P. A.; Gordy, W. (1966). "Journal of Molecular Spectroscopy" 21: 291.

sciencemag.org

blogs.sciencemag.org

Lowe, Derek (2009). "Copia arquivada". Science Translational Medicine. Arquivado dende o orixinal o 26 de xullo de 2020. Consultado o 30 de agosto de 2020. |title= e |título= redundantes (Axuda); |urlarquivo= e |url-arquivo= redundantes (Axuda); |dataarquivo= e |data-arquivo= redundantes (Axuda)

tedpella.com

"Material Safety Data Sheet" (PDF). Arquivado dende o orixinal (PDF) o 17 de novembro de 2016. Consultado o 30 de agosto de 2020.

web.archive.org

"Material Safety Data Sheet" (PDF). Arquivado dende o orixinal (PDF) o 17 de novembro de 2016. Consultado o 30 de agosto de 2020.
"Archived copy" (PDF). Ashford's Dictionary of Industrial Chemicals, Third edition. p. 76. Arquivado dende o orixinal (PDF) o 16 de maio de 2011. Consultado o 2011-03-31.
Spanish Ministry of Health (2002). Acetonitrile. Summary Risk Assessment Report (PDF). Ispra (VA), Italy: European Chemicals Bureau. Special Publication I.01.65. Arquivado dende o orixinal (PDF) o 17 de decembro de 2008. Consultado o 30 de agosto de 2020.
Patente US 4179462 Arquivado 05 de abril de 2022 en Wayback Machine., Olive, G. & Olive, S., "Process for preparing acetonitrile", published 1979-12-18, assigned to Monsanto Company
Lowe, Derek (2009). "Copia arquivada". Science Translational Medicine. Arquivado dende o orixinal o 26 de xullo de 2020. Consultado o 30 de agosto de 2020. |title= e |título= redundantes (Axuda); |urlarquivo= e |url-arquivo= redundantes (Axuda); |dataarquivo= e |data-arquivo= redundantes (Axuda)
Institut national de recherche et de sécurité (INRS) (2004). Fiche toxicologique no. 104 : Acétonitrile (PDF). Paris: INRS. ISBN 2-7389-1278-8. Arquivado dende o orixinal (PDF) o 28 de xullo de 2011. Consultado o 2008-08-19.
"Twenty-Fifth Commission Directive 2000/11/EC of 10 March 2000 adapting to technical progress Annex II to Council Directive 76/768/EEC on the approximation of laws of the Member States relating to cosmetic products". Official Journal of the European Communities L65: 22–25. 2000-03-14. Arquivado dende o orixinal o 30 de maio de 2013. Consultado o 30 de agosto de 2020.

worldcat.org

Jürgen-Hinrich., Fuhrhop (2003). Organic synthesis : concepts and methods. Li, Guangtao, Dr. (3rd, completely rev. and enl. ed.). Weinheim: Wiley-VCH. p. 26. ISBN 9783527302727. OCLC 51068223.