Naphthalene (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Naphthalene" in English language version.

refsWebsite

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14doi.org

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4harvard.edu

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abc.net.au

"New propulsion system using the key ingredient in moth balls could propel satellites through space". Australian Broadcasting Corporation. 8 December 2021. Retrieved December 11, 2021.

aip.org

pubs.aip.org

Bornmann, John A. (1962). "Semiconductivity of Naphthalene". The Journal of Chemical Physics. 36 (6): 1691–1692. Bibcode:1962JChPh..36.1691B. doi:10.1063/1.1732805. ISSN 0021-9606.

aps.org

link.aps.org

Schein, L. B.; Duke, C. B.; McGhie, A. R. (1978). "Observation of the Band-Hopping Transition for Electrons in Naphthalene". Physical Review Letters. 40 (3): 197–200. Bibcode:1978PhRvL..40..197S. doi:10.1103/PhysRevLett.40.197. ISSN 0031-9007.

archive.org

Seidell, Atherton; Linke, William F. (1919). Solubility of Inorganic and Organic Compounds (2nd ed.). New York: D. Van Nostrand Company. pp. 443–446.

bbc.co.uk

news.bbc.co.uk

"Termite 'mothball' keep insects at bay". Sci/Tech. BBC News. April 8, 1998.

books.google.com

Douglas, Bodie E.; Ho, Shih-Ming (2007). Structure and Chemistry of Crystalline Solids. New York: Springer Science+Business Media, Inc. p. 288. ISBN 978-0-387-26147-8.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0439". National Institute for Occupational Safety and Health (NIOSH).
"Naphthalene". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
"CDC - NIOSH Pocket Guide to Chemical Hazards - Naphthalene". Cdc.gov. Retrieved 6 March 2022.

chemister.ru

Anatolievich, Kiper Ruslan. "naphthalene". chemister.ru. Retrieved 2014-06-21.

ddbst.com

"Thermal Conductivity of Naphthalene". DDBST GmbH. Archived from the original on 2016-03-04. Retrieved 2014-06-21.
"Dynamic Viscosity of Naphthalene". DDBST GmbH. Archived from the original on 2016-03-04. Retrieved 2014-06-21.

doi.org

Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 13, 35, 204, 207, 221–222, 302, 457, 461, 469, 601, 650. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
Amoore JE, Hautala E (1983). "Odor as an aid to chemical safety: Odor thresholds compared with threshold limit values and volatiles for 214 industrial chemicals in air and water dilution". J Appl Toxicol. 3 (6): 272–290. doi:10.1002/jat.2550030603. PMID 6376602. S2CID 36525625.
John Kidd (1821). "Observations on Naphthalene, a peculiar substance resembling a concrete essential oil, which is produced during the decomposition of coal tar, by exposure to a red heat". Philosophical Transactions. 111: 209–221. doi:10.1098/rstl.1821.0017. S2CID 97798085.
Emil Erlenmeyer (1866). "Studien über die s. g. aromatischen Säuren". Annalen der Chemie und Pharmacie. 137 (3): 327–359. doi:10.1002/jlac.18661370309.
Cruickshank, D. W. J.; Sparks, R. A. (18 October 1960). "Experimental and Theoretical Determinations of Bond Lengths in Naphthalene, Anthracene and Other Hydrocarbons". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences. 258 (1293): 270–285. Bibcode:1960RSPSA.258..270C. doi:10.1098/rspa.1960.0187. S2CID 96765335.
Dieter Cremer; Thomas Schmidt; Charles W. Bock (1985). "Theoretical determination of molecular structure and conformation. 14. Is bicyclo[6.2.0]decapentaene aromatic or antiaromatic?". J. Org. Chem. 50 (15): 2684–2688. doi:10.1021/jo00215a018.
Bornmann, John A. (1962). "Semiconductivity of Naphthalene". The Journal of Chemical Physics. 36 (6): 1691–1692. Bibcode:1962JChPh..36.1691B. doi:10.1063/1.1732805. ISSN 0021-9606.
Schein, L. B.; Duke, C. B.; McGhie, A. R. (1978). "Observation of the Band-Hopping Transition for Electrons in Naphthalene". Physical Review Letters. 40 (3): 197–200. Bibcode:1978PhRvL..40..197S. doi:10.1103/PhysRevLett.40.197. ISSN 0031-9007.
van Soolingen J, de Lang RJ, den Besten R, et al. (1995). "A simple procedure for the preparation of 1,8-bis(diphenylphosphino)naphthalene". Synthetic Communications. 25 (11): 1741–1744. doi:10.1080/00397919508015858.
Daisy BH, Strobel GA, Castillo U, et al. (November 2002). "Naphthalene, an insect repellent, is produced by Muscodor vitigenus, a novel endophytic fungus". Microbiology. 148 (Pt 11): 3737–41. doi:10.1099/00221287-148-11-3737. PMID 12427963.
K. Komatsua; Y. Murataa; N. Sugitaa; et al. (1993). "Use of naphthalene as a solvent for selective formation of the 1:1 Diels–Alder adduct of C₆₀ with anthracene". Tetrahedron Letters. 34 (52): 8473–8476. doi:10.1016/S0040-4039(00)61362-X.
M.A. Filatov; A.V. Cheprakov (2011). "The synthesis of new tetrabenzo- and tetranaphthoporphyrins via the addition reactions of 4,7-dihydroisoindole". Tetrahedron. 67 (19): 3559–3566. doi:10.1016/j.tet.2011.01.052.
Tsifakis, Dimitrios; Charles, Christine; Boswell, Rod (2020-09-23). "Naphthalene as a Cubesat Cold Gas Thruster Propellant". Frontiers in Physics. 8: 389. Bibcode:2020FrP.....8..389T. doi:10.3389/fphy.2020.00389. hdl:1885/229663.
Santucci K, Shah B (Jan 2000). "Association of naphthalene with acute hemolytic anemia". Acad Emerg Med. 7 (1): 42–7. doi:10.1111/j.1553-2712.2000.tb01889.x. PMID 10894241.

dse.vic.gov.au

"Summary of Possum Repellent Study". Archived from the original on September 28, 2013.

environmentalhealth.ca

"Mothballs, air fresheners and cancer". Environmental Health Association of Nova Scotia. Retrieved 24 May 2013.

epa.gov

"Polycyclic Aromatic Hydrocarbons (PAHs)" (PDF). Archived (PDF) from the original on 2014-11-30. Naphthalene is a PAH that is produced commercially in the US
"Naphthalene" (PDF). Epa.gov. Archived (PDF) from the original on 2016-10-14. Retrieved 6 March 2022.

water.epa.gov

"Ambient Water Quality Criteria for Naphthalene" (PDF). United States Environmental Protection Agency. 2014-04-23. Retrieved 2014-06-21.

ghostarchive.org

Alderson, Andrew (15 Nov 2008). "Holy straight bananas – now the Eurocrats are banning moth balls". The Telegraph. Archived from the original on 2022-01-12. Retrieved 2013-11-23.

handle.net

hdl.handle.net

Tsifakis, Dimitrios; Charles, Christine; Boswell, Rod (2020-09-23). "Naphthalene as a Cubesat Cold Gas Thruster Propellant". Frontiers in Physics. 8: 389. Bibcode:2020FrP.....8..389T. doi:10.3389/fphy.2020.00389. hdl:1885/229663.

harvard.edu

ui.adsabs.harvard.edu

Cruickshank, D. W. J.; Sparks, R. A. (18 October 1960). "Experimental and Theoretical Determinations of Bond Lengths in Naphthalene, Anthracene and Other Hydrocarbons". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences. 258 (1293): 270–285. Bibcode:1960RSPSA.258..270C. doi:10.1098/rspa.1960.0187. S2CID 96765335.
Bornmann, John A. (1962). "Semiconductivity of Naphthalene". The Journal of Chemical Physics. 36 (6): 1691–1692. Bibcode:1962JChPh..36.1691B. doi:10.1063/1.1732805. ISSN 0021-9606.
Schein, L. B.; Duke, C. B.; McGhie, A. R. (1978). "Observation of the Band-Hopping Transition for Electrons in Naphthalene". Physical Review Letters. 40 (3): 197–200. Bibcode:1978PhRvL..40..197S. doi:10.1103/PhysRevLett.40.197. ISSN 0031-9007.
Tsifakis, Dimitrios; Charles, Christine; Boswell, Rod (2020-09-23). "Naphthalene as a Cubesat Cold Gas Thruster Propellant". Frontiers in Physics. 8: 389. Bibcode:2020FrP.....8..389T. doi:10.3389/fphy.2020.00389. hdl:1885/229663.

hathitrust.org

babel.hathitrust.org

C. Graebe (1869) "Ueber die Constitution des Naphthalins" (On the structure of naphthalene), Annalen der Chemie und Pharmacie, 149 : 20–28.

iarc.fr

monographs.iarc.fr

IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. ISBN 978-92-832-1282-9. Retrieved December 25, 2008. {{cite book}}: |work= ignored (help)

medlineplus.gov

MedlinePlus Encyclopedia: Naphthalene poisoning

nih.gov

pubmed.ncbi.nlm.nih.gov

Amoore JE, Hautala E (1983). "Odor as an aid to chemical safety: Odor thresholds compared with threshold limit values and volatiles for 214 industrial chemicals in air and water dilution". J Appl Toxicol. 3 (6): 272–290. doi:10.1002/jat.2550030603. PMID 6376602. S2CID 36525625.
Daisy BH, Strobel GA, Castillo U, et al. (November 2002). "Naphthalene, an insect repellent, is produced by Muscodor vitigenus, a novel endophytic fungus". Microbiology. 148 (Pt 11): 3737–41. doi:10.1099/00221287-148-11-3737. PMID 12427963.
Santucci K, Shah B (Jan 2000). "Association of naphthalene with acute hemolytic anemia". Acad Emerg Med. 7 (1): 42–7. doi:10.1111/j.1553-2712.2000.tb01889.x. PMID 10894241.

ntp.niehs.nih.gov

"NTP Technical Reports 410 and 500". NTP Technical Reports 410 and 500, available from NTP: Long-Term Abstracts & Reports. Archived from the original on October 24, 2004. Retrieved March 6, 2005.

nist.gov

webbook.nist.gov

Naphthalene in Linstrom, Peter J.; Mallard, William G. (eds.); NIST Chemistry WebBook, NIST Standard Reference Database Number 69, National Institute of Standards and Technology, Gaithersburg (MD) (retrieved 2014-05-24)

oehha.org

Proposition 65 Archived 2019-07-29 at the Wayback Machine, Office of Environmental Health Hazard Assessment

physorg.com

"Scientists May Have Solved Mystery Of Carcinogenic Mothballs", Physorg.com, June 20, 2006.

semanticscholar.org

api.semanticscholar.org

Amoore JE, Hautala E (1983). "Odor as an aid to chemical safety: Odor thresholds compared with threshold limit values and volatiles for 214 industrial chemicals in air and water dilution". J Appl Toxicol. 3 (6): 272–290. doi:10.1002/jat.2550030603. PMID 6376602. S2CID 36525625.
John Kidd (1821). "Observations on Naphthalene, a peculiar substance resembling a concrete essential oil, which is produced during the decomposition of coal tar, by exposure to a red heat". Philosophical Transactions. 111: 209–221. doi:10.1098/rstl.1821.0017. S2CID 97798085.
Cruickshank, D. W. J.; Sparks, R. A. (18 October 1960). "Experimental and Theoretical Determinations of Bond Lengths in Naphthalene, Anthracene and Other Hydrocarbons". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences. 258 (1293): 270–285. Bibcode:1960RSPSA.258..270C. doi:10.1098/rspa.1960.0187. S2CID 96765335.

sgmjournals.org

mic.sgmjournals.org

Daisy BH, Strobel GA, Castillo U, et al. (November 2002). "Naphthalene, an insect repellent, is produced by Muscodor vitigenus, a novel endophytic fungus". Microbiology. 148 (Pt 11): 3737–41. doi:10.1099/00221287-148-11-3737. PMID 12427963.

sigmaaldrich.com

Sigma-Aldrich Co., Naphthalene.

telegraph.co.uk

Alderson, Andrew (15 Nov 2008). "Holy straight bananas – now the Eurocrats are banning moth balls". The Telegraph. Archived from the original on 2022-01-12. Retrieved 2013-11-23.

web.archive.org

"Thermal Conductivity of Naphthalene". DDBST GmbH. Archived from the original on 2016-03-04. Retrieved 2014-06-21.
"Dynamic Viscosity of Naphthalene". DDBST GmbH. Archived from the original on 2016-03-04. Retrieved 2014-06-21.
"Polycyclic Aromatic Hydrocarbons (PAHs)" (PDF). Archived (PDF) from the original on 2014-11-30. Naphthalene is a PAH that is produced commercially in the US
"Summary of Possum Repellent Study". Archived from the original on September 28, 2013.
"NTP Technical Reports 410 and 500". NTP Technical Reports 410 and 500, available from NTP: Long-Term Abstracts & Reports. Archived from the original on October 24, 2004. Retrieved March 6, 2005.
Proposition 65 Archived 2019-07-29 at the Wayback Machine, Office of Environmental Health Hazard Assessment
"Naphthalene" (PDF). Epa.gov. Archived (PDF) from the original on 2016-10-14. Retrieved 6 March 2022.

worldcat.org

search.worldcat.org

Bornmann, John A. (1962). "Semiconductivity of Naphthalene". The Journal of Chemical Physics. 36 (6): 1691–1692. Bibcode:1962JChPh..36.1691B. doi:10.1063/1.1732805. ISSN 0021-9606.
Schein, L. B.; Duke, C. B.; McGhie, A. R. (1978). "Observation of the Band-Hopping Transition for Electrons in Naphthalene". Physical Review Letters. 40 (3): 197–200. Bibcode:1978PhRvL..40..197S. doi:10.1103/PhysRevLett.40.197. ISSN 0031-9007.

yourlocalguardian.co.uk

Gray, Kerrina (17 November 2013). "Council warned against use of poisonous moth balls". Your Local Guardian. Newsquest (London) Ltd. Retrieved 2012-11-23.

zenodo.org

Emil Erlenmeyer (1866). "Studien über die s. g. aromatischen Säuren". Annalen der Chemie und Pharmacie. 137 (3): 327–359. doi:10.1002/jlac.18661370309.