Pyridine (English Wikipedia)

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

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64doi.org

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agrochemex.net

"Pyridine's Development in China". AgroChemEx. 11 May 2010. Archived from the original on 20 September 2018. Retrieved 7 January 2011.

alfa.com

"Pyridine MSDS" (PDF). Alfa Aesar. Archived from the original (PDF) on 3 April 2015. Retrieved 3 June 2010.

archive.today

"About Vertellus". vertellus.com. Archived from the original on 18 September 2012. Retrieved 7 January 2011.

bnf.fr

gallica.bnf.fr

Chichibabin, A. E. (1924). "Über Kondensation der Aldehyde mit Ammoniak zu Pyridinebasen" [On condensation of aldehydes with ammonia to make pyridines]. Journal für Praktische Chemie. 107: 122. doi:10.1002/prac.19241070110. Archived from the original on 20 September 2018. Retrieved 7 January 2011.

books.google.com

Joule, p. 16 Joule, J. A.; Mills, K. (2010). Heterocyclic Chemistry (5th ed.). Chichester: Blackwell Publishing. ISBN 978-1-4051-3300-5.
Joule, p. 7 Joule, J. A.; Mills, K. (2010). Heterocyclic Chemistry (5th ed.). Chichester: Blackwell Publishing. ISBN 978-1-4051-3300-5.
Koerner, W. (1869). "Synthèse d'une base isomère à la toluidine" [Synthesis of a base [that is] isomeric to toluidine]. Giornale di Scienze Naturali ed Economiche (Journal of Natural Science and Economics (Palermo, Italy)) (in French). 5: 111–114.
Bansal, Raj K. (1999). Heterocyclic Chemistry. New Age International. p. 216. ISBN 81-224-1212-2.
Joule, pp. 125–141 Joule, J. A.; Mills, K. (2010). Heterocyclic Chemistry (5th ed.). Chichester: Blackwell Publishing. ISBN 978-1-4051-3300-5.
Joule, p. 126 Joule, J. A.; Mills, K. (2010). Heterocyclic Chemistry (5th ed.). Chichester: Blackwell Publishing. ISBN 978-1-4051-3300-5.
Joule, p. 133 Joule, J. A.; Mills, K. (2010). Heterocyclic Chemistry (5th ed.). Chichester: Blackwell Publishing. ISBN 978-1-4051-3300-5.
Tojo, G.; Fernandez, M. (2006). Oxidation of alcohols to aldehydes and ketones: a guide to current common practice. New York: Springer. pp. 28, 29, 86. ISBN 0-387-23607-4.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0541". National Institute for Occupational Safety and Health (NIOSH).
"Pyridine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

dguv.de

gestis.dguv.de

Record of Pyridine in the GESTIS Substance Database of the Institute for Occupational Safety and Health

doi.org

Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 141. doi:10.1039/9781849733069-FP001 (inactive 12 April 2024). ISBN 978-0-85404-182-4.{{cite book}}: CS1 maint: DOI inactive as of April 2024 (link)
Shimizu, S.; Watanabe, N.; Kataoka, T.; Shoji, T.; Abe, N.; Morishita, S.; Ichimura, H. "Pyridine and Pyridine Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_399. ISBN 978-3527306732.
Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Cox, E. (1958). "Crystal Structure of Benzene". Reviews of Modern Physics. 30 (1): 159–162. Bibcode:1958RvMP...30..159C. doi:10.1103/RevModPhys.30.159.
McCullough, J. P.; Douslin, D. R.; Messerly, J. F.; Hossenlopp, I. A.; Kincheloe, T. C.; Waddington, Guy (1957). "Pyridine: Experimental and Calculated Chemical Thermodynamic Properties between 0 and 1500 K.; a Revised Vibrational Assignment". Journal of the American Chemical Society. 79 (16): 4289. doi:10.1021/ja01573a014.
Mootz, D. (1981). "Crystal structures of pyridine and pyridine trihydrate". The Journal of Chemical Physics. 75 (3): 1517–1522. Bibcode:1981JChPh..75.1517M. doi:10.1063/1.442204.
Anderson, Thomas (1849). "On the constitution and properties of picoline, a new organic base from coal-tar". Transactions of the Royal Societies of Edinburgh University. 16 (2): 123–136. doi:10.1017/S0080456800024984. S2CID 100301190. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, T. (1849). "Producte der trocknen Destillation thierischer Materien" [Products of the dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 70: 32–38. doi:10.1002/jlac.18490700105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, Thomas (1851). "On the products of the destructive distillation of animal substances. Part II". Transactions of the Royal Society of Edinburgh. 20 (2): 247–260. doi:10.1017/S0080456800033160. S2CID 102143621. Archived from the original on 24 May 2020. Retrieved 24 September 2018. From p. 253: "Pyridine. The first of these bases, to which I give the name of pyridine, … "
Anderson, T. (1851). "Ueber die Producte der trocknen Destillation thierischer Materien" [On the products of dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 80: 44–65. doi:10.1002/jlac.18510800104. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Ladenburg, A. (1884). "Synthese des Piperidins" [Synthesis of piperidine]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 156. doi:10.1002/cber.18840170143. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ladenburg, A. (1884). "Synthese des Piperidins und seiner Homologen" [Synthesis of piperidine and its homologues]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 388–391. doi:10.1002/cber.188401701110. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ramsay, William (1876). "On picoline and its derivatives". Philosophical Magazine. 5th series. 2 (11): 269–281. doi:10.1080/14786447608639105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
"A. Henninger, aus Paris. 12. April 1877". Berichte der Deutschen Chemischen Gesellschaft (Correspondence). 10: 727–737. 1877. doi:10.1002/cber.187701001202.
Hantzsch, A. (1881). "Condensationsprodukte aus Aldehydammoniak und ketonartigen Verbindungen" [Condensation products from aldehyde ammonia and ketone-type compounds]. Berichte der Deutschen Chemischen Gesellschaft. 14 (2): 1637–1638. doi:10.1002/cber.18810140214. Archived from the original on 22 January 2021. Retrieved 6 September 2019.
Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese" [Syntheses in the pyridine series. On an extension of the Hantzsch dihydropyridine synthesis]. Berichte der Deutschen Chemischen Gesellschaft. 31: 761–767. doi:10.1002/cber.189803101157. Archived from the original on 15 January 2020. Retrieved 29 June 2019.
Chichibabin, A. E. (1924). "Über Kondensation der Aldehyde mit Ammoniak zu Pyridinebasen" [On condensation of aldehydes with ammonia to make pyridines]. Journal für Praktische Chemie. 107: 122. doi:10.1002/prac.19241070110. Archived from the original on 20 September 2018. Retrieved 7 January 2011.
Tang, Jian; Jin, Qi Zhang; Shen, Guo Hui; Ho, Chi Tang; Chang, Stephen S. (1983). "Isolation and identification of volatile compounds from fried chicken". Journal of Agricultural and Food Chemistry. 31 (6): 1287. doi:10.1021/jf00120a035.
Shibamoto, Takayuki; Kamiya, Yoko; Mihara, Satoru (1981). "Isolation and identification of volatile compounds in cooked meat: sukiyaki". Journal of Agricultural and Food Chemistry. 29: 57–63. doi:10.1021/jf00103a015.
Aeschbacher, HU; Wolleb, U; Löliger, J; Spadone, JC; Liardon, R (1989). "Contribution of coffee aroma constituents to the mutagenicity of coffee". Food and Chemical Toxicology. 27 (4): 227–232. doi:10.1016/0278-6915(89)90160-9. PMID 2659457.
Buttery, Ron G.; Seifert, Richard M.; Guadagni, Dante G.; Ling, Louisa C. (1971). "Characterization of Volatile Pyrazine and Pyridine Components of Potato Chips". Journal of Agricultural and Food Chemistry. 19 (5). Washington, DC: ACS: 969–971. doi:10.1021/jf60177a020.
Ho, Chi Tang; Lee, Ken N.; Jin, Qi Zhang (1983). "Isolation and identification of volatile flavor compounds in fried bacon". Journal of Agricultural and Food Chemistry. 31 (2): 336. doi:10.1021/jf00116a038.
Dumont, Jean Pierre; Adda, Jacques (1978). "Occurrence of sesquiterpene in mountain cheese volatiles". Journal of Agricultural and Food Chemistry. 26 (2): 364. doi:10.1021/jf60216a037.
Labows, John N. Jr.; Warren, Craig B. (1981). "Odorants as Chemical Messengers". In Moskowitz, Howard R. (ed.). Odor Quality and Chemical Structure. Washington, DC: American Chemical Society. pp. 195–210. doi:10.1021/bk-1981-0148.fw001. ISBN 9780841206076.
Vitzthum, Otto G.; Werkhoff, Peter; Hubert, Peter (1975). "New volatile constituents of black tea flavor". Journal of Agricultural and Food Chemistry. 23 (5): 999. doi:10.1021/jf60201a032.
Kostelc, J. G.; Preti, G.; Nelson, P. R.; Brauner, L.; Baehni, P. (1984). "Oral Odors in Early Experimental Gingivitis". Journal of Periodontal Research. 19 (3): 303–312. doi:10.1111/j.1600-0765.1984.tb00821.x. PMID 6235346.
Frank, R. L.; Seven, R. P. (1949). "Pyridines. IV. A Study of the Chichibabin Synthesis". Journal of the American Chemical Society. 71 (8): 2629–2635. doi:10.1021/ja01176a008.
Scott, T. A. (1967). "A method for the Degradation of Radioactive Nicotinic Acid". Biochemical Journal. 102 (1): 87–93. doi:10.1042/bj1020087. PMC 1270213. PMID 6030305.
Kroehnke, Fritz (1976). "The Specific Synthesis of Pyridines and Oligopyridines". Synthesis. 1976 (1): 1–24. doi:10.1055/s-1976-23941. S2CID 95238046..
Ciamician, G. L.; Dennstedt, M. (1881). "Ueber die Einwirkung des Chloroforms auf die Kaliumverbindung Pyrrols". Berichte der Deutschen Chemischen Gesellschaft. 14 (1): 1153–1163. doi:10.1002/cber.188101401240. ISSN 0365-9496.
Skell, P. S.; Sandler, R. S. (1958). "Reactions of 1,1-Dihalocyclopropanes with Electrophilic Reagents. Synthetic Route for Inserting a Carbon Atom Between the Atoms of a Double Bond". Journal of the American Chemical Society. 80 (8): 2024. doi:10.1021/ja01541a070.
Jones, R. L.; Rees, C. W. (1969). "Mechanism of heterocyclic ring expansions. Part III. Reaction of pyrroles with dichlorocarbene". Journal of the Chemical Society C: Organic (18): 2249. doi:10.1039/J39690002249.
Gambacorta, A.; Nicoletti, R.; Cerrini, S.; Fedeli, W.; Gavuzzo, E. (1978). "Trapping and structure determination of an intermediate in the reaction between 2-methyl-5-t-butylpyrrole and dichlorocarbene". Tetrahedron Letters. 19 (27): 2439. doi:10.1016/S0040-4039(01)94795-1.
Gattermann, L.; Skita, A. (1916). "Eine Synthese von Pyridin-Derivaten" [A synthesis of pyridine derivatives]. Chemische Berichte. 49 (1): 494–501. doi:10.1002/cber.19160490155. Archived from the original on 25 September 2020. Retrieved 29 June 2019.
Karpeiskii, Y.; Florent'ev V. L. (1969). "Condensation of Oxazoles with Dienophiles — a New Method for the Synthesis of Pyridine Bases". Russian Chemical Reviews. 38 (7): 540–546. Bibcode:1969RuCRv..38..540K. doi:10.1070/RC1969v038n07ABEH001760. S2CID 250852496.
Tarr, J. B.; Arditti, J. (1982). "Niacin Biosynthesis in Seedlings of Zea mays". Plant Physiology. 69 (3): 553–556. doi:10.1104/pp.69.3.553. PMC 426252. PMID 16662247.
Campaigne, E. (1986). "Adrien Albert and the Rationalization of Heterocyclic chemistry". J. Chem. Educ. 63 (10): 860. Bibcode:1986JChEd..63..860C. doi:10.1021/ed063p860.
Krygowski, T. M.; Szatyowicz, H.; Zachara, J. E. (2005). "How H-bonding Modifies Molecular Structure and π-Electron Delocalization in the Ring of Pyridine/Pyridinium Derivatives Involved in H-Bond Complexation". J. Org. Chem. 70 (22): 8859–8865. doi:10.1021/jo051354h. PMID 16238319.
Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Bakke, Jan M.; Hegbom, Ingrid (1994). "Dinitrogen Pentoxide-Sulfur Dioxide, a New nitrate ion system". Acta Chemica Scandinavica. 48: 181–182. doi:10.3891/acta.chem.scand.48-0181.
Ono, Noboru; Murashima, Takashi; Nishi, Keiji; Nakamoto, Ken-Ichi; Kato, Atsushi; Tamai, Ryuji; Uno, Hidemitsu (2002). "Preparation of Novel Heteroisoindoles from nitropyridines and Nitropyridones". Heterocycles. 58: 301. doi:10.3987/COM-02-S(M)22 (inactive 17 February 2024).{{cite journal}}: CS1 maint: DOI inactive as of February 2024 (link)
Duffy, Joseph L.; Laali, Kenneth K. (1991). "Aprotic Nitration (NO⁺
₂BF⁻
₄) of 2-Halo- and 2,6-Dihalopyridines and Transfer-Nitration Chemistry of Their N-Nitropyridinium Cations". The Journal of Organic Chemistry. 56 (9): 3006. doi:10.1021/jo00009a015.
Möller, Ernst Friedrich; Birkofer, Leonhard (1942). "Konstitutionsspezifität der Nicotinsäure als Wuchsstoff bei Proteus vulgaris und Streptobacterium plantarum" [Constitutional specificity of nicotinic acid as a growth factor in Proteus vulgaris and Streptobacterium plantarum]. Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 75 (9): 1108. doi:10.1002/cber.19420750912.
Mosher, H. S.; Turner, L.; Carlsmith, A. (1953). "Pyridine-N-oxide". Org. Synth. 33: 79. doi:10.15227/orgsyn.033.0079.
Campeau, Louis-Charles; Fagnou, Keith (2011). "Synthesis of 2-aryl Pyridines By Palladium-catalyzed Direct Arylation of Pyridine N-oxides". Org. Synth. 88: 22. doi:10.15227/orgsyn.088.0022.
Shreve, R. Norris; Riechers, E. H.; Rubenkoenig, Harry; Goodman, A. H. (1940). "Amination in the Heterocyclic Series by Sodium amide". Industrial & Engineering Chemistry. 32 (2): 173. doi:10.1021/ie50362a008.
Badger, G; Sasse, W (1963). "The Action of Metal Catalysts on Pyridines". Advances in Heterocyclic Chemistry Volume 2. Vol. 2. pp. 179–202. doi:10.1016/S0065-2725(08)60749-7. ISBN 9780120206025. PMID 14279523.
Sasse, W. H. F. (1966). "2,2'-bipyridine" (PDF). Organic Syntheses. 46: 5–8. doi:10.1002/0471264180.os046.02. ISBN 0471264229. Archived from the original (PDF) on 21 January 2012.
Tanner, Dennis D.; Yang, Chi Ming (1993). "On the structure and mechanism of formation of the Lansbury reagent, lithium tetrakis(N-dihydropyridyl) aluminate". The Journal of Organic Chemistry. 58 (7): 1840. doi:10.1021/jo00059a041.
De Koning, A.; Budzelaar, P. H. M.; Boersma, J.; Van Der Kerk, G. J. M. (1980). "Specific and selective reduction of aromatic nitrogen heterocycles with the bis-pyridine complexes of bis(1,4-dihydro-1-pyridyl)zinc and bis(1,4-dihydro-1-pyridyl)magnesium". Journal of Organometallic Chemistry. 199 (2): 153. doi:10.1016/S0022-328X(00)83849-8.
Ferles, M. (1959). "Studies in the pyridine series. II. Ladenburg and electrolytic reductions of pyridine bases". Collection of Czechoslovak Chemical Communications. 24 (4). Institute of Organic Chemistry & Biochemistry: 1029–1035. doi:10.1135/cccc19591029.
Donohoe, Timothy J.; McRiner, Andrew J.; Sheldrake, Peter (2000). "Partial Reduction of Electron-Deficient Pyridines". Organic Letters. 2 (24): 3861–3863. doi:10.1021/ol0065930. PMID 11101438.
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. The plots shown in this paper used older parameters. Improved E&C parameters are listed in ECW model.
Crabtree, Robert (1979). "Iridium compounds in catalysis". Accounts of Chemical Research. 12 (9): 331–337. doi:10.1021/ar50141a005.
Sherman, A. R. (2004). "Pyridine". In Paquette, L. (ed.). Encyclopedia of Reagents for Organic Synthesis. e-EROS (Encyclopedia of Reagents for Organic Synthesis). New York: J. Wiley & Sons. doi:10.1002/047084289X.rp280. ISBN 0471936235.
Junk, G. A.; Ford, C. S. (1980). "A review of organic emissions from selected combustion processes". Chemosphere. 9 (4): 187. Bibcode:1980Chmsp...9..187J. doi:10.1016/0045-6535(80)90079-X. OSTI 5295035.
Hawthorne, Steven B.; Sievers, Robert E. (1984). "Emissions of organic air pollutants from shale oil wastewaters". Environmental Science & Technology. 18 (6): 483–90. Bibcode:1984EnST...18..483H. doi:10.1021/es00124a016. PMID 22247953.
Stuermer, Daniel H.; Ng, Douglas J.; Morris, Clarence J. (1982). "Organic contaminants in groundwater near to underground coal gasification site in northeastern Wyoming". Environmental Science & Technology. 16 (9): 582–7. Bibcode:1982EnST...16..582S. doi:10.1021/es00103a009. PMID 22284199.
Sims, G. K.; O'Loughlin, E. J. (1989). "Degradation of pyridines in the environment". CRC Critical Reviews in Environmental Control. 19 (4): 309–340. doi:10.1080/10643388909388372.
Sims, G. K.; Sommers, L.E. (1986). "Biodegradation of pyridine derivatives in soil suspensions". Environmental Toxicology and Chemistry. 5 (6): 503–509. doi:10.1002/etc.5620050601.
Sims, G. K.; O'Loughlin, E.J. (1992). "Riboflavin production during growth of Micrococcus luteus on pyridine". Applied and Environmental Microbiology. 58 (10): 3423–3425. Bibcode:1992ApEnM..58.3423S. doi:10.1128/AEM.58.10.3423-3425.1992. PMC 183117. PMID 16348793.
Bi, E.; Schmidt, T. C.; Haderlein, S. B. (2006). "Sorption of heterocyclic organic compounds to reference soils: column studies for process identification". Environ Sci Technol. 40 (19): 5962–5970. Bibcode:2006EnST...40.5962B. doi:10.1021/es060470e. PMID 17051786.
O'Loughlin, E. J; Traina, S. J.; Sims, G. K. (2000). "Effects of sorption on the biodegradation of 2-methylpyridine in aqueous suspensions of reference clay minerals". Environmental Toxicology and Chemistry. 19 (9): 2168–2174. doi:10.1002/etc.5620190904. S2CID 98654832.
Powell, W. H. (1983). "Revision of the extended Hantzsch-Widman system of nomenclature for hetero mono-cycles" (PDF). Pure and Applied Chemistry. 55 (2): 409–416. doi:10.1351/pac198855020409. S2CID 4686578. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.

epa.gov

cfpub.epa.gov

"Database of the (EPA)". U.S. Environmental Protection Agency. Archived from the original on 18 September 2011. Retrieved 7 January 2011.

espacenet.com

worldwide.espacenet.com

DE patent 1917037, Swift, Graham, "Verfahren zur Herstellung von Pyridin und Methylpyridinen", issued 1968
JP patent 7039545, Nippon Kayaku, "Electrically-assisted bicycle, driving system thereof, and manufacturing method", issued 1967
BE patent 758201, Koei Chemical, "Procede de preparation de bases pyridiques", issued 1969

fda.gov

"FDA Removes 7 Synthetic Flavoring Substances from Food Additives List". 5 October 2018. Archived from the original on 7 October 2018. Retrieved 8 October 2018.

federalregister.gov

83 FR 50490

fishersci.com

fscimage.fishersci.com

"Pyridine MSDS". fishersci.com. Fisher. Archived from the original on 11 June 2010. Retrieved 2 February 2010.

harvard.edu

ui.adsabs.harvard.edu

Cox, E. (1958). "Crystal Structure of Benzene". Reviews of Modern Physics. 30 (1): 159–162. Bibcode:1958RvMP...30..159C. doi:10.1103/RevModPhys.30.159.
Mootz, D. (1981). "Crystal structures of pyridine and pyridine trihydrate". The Journal of Chemical Physics. 75 (3): 1517–1522. Bibcode:1981JChPh..75.1517M. doi:10.1063/1.442204.
Karpeiskii, Y.; Florent'ev V. L. (1969). "Condensation of Oxazoles with Dienophiles — a New Method for the Synthesis of Pyridine Bases". Russian Chemical Reviews. 38 (7): 540–546. Bibcode:1969RuCRv..38..540K. doi:10.1070/RC1969v038n07ABEH001760. S2CID 250852496.
Campaigne, E. (1986). "Adrien Albert and the Rationalization of Heterocyclic chemistry". J. Chem. Educ. 63 (10): 860. Bibcode:1986JChEd..63..860C. doi:10.1021/ed063p860.
Junk, G. A.; Ford, C. S. (1980). "A review of organic emissions from selected combustion processes". Chemosphere. 9 (4): 187. Bibcode:1980Chmsp...9..187J. doi:10.1016/0045-6535(80)90079-X. OSTI 5295035.
Hawthorne, Steven B.; Sievers, Robert E. (1984). "Emissions of organic air pollutants from shale oil wastewaters". Environmental Science & Technology. 18 (6): 483–90. Bibcode:1984EnST...18..483H. doi:10.1021/es00124a016. PMID 22247953.
Stuermer, Daniel H.; Ng, Douglas J.; Morris, Clarence J. (1982). "Organic contaminants in groundwater near to underground coal gasification site in northeastern Wyoming". Environmental Science & Technology. 16 (9): 582–7. Bibcode:1982EnST...16..582S. doi:10.1021/es00103a009. PMID 22284199.
Sims, G. K.; O'Loughlin, E.J. (1992). "Riboflavin production during growth of Micrococcus luteus on pyridine". Applied and Environmental Microbiology. 58 (10): 3423–3425. Bibcode:1992ApEnM..58.3423S. doi:10.1128/AEM.58.10.3423-3425.1992. PMC 183117. PMID 16348793.
Bi, E.; Schmidt, T. C.; Haderlein, S. B. (2006). "Sorption of heterocyclic organic compounds to reference soils: column studies for process identification". Environ Sci Technol. 40 (19): 5962–5970. Bibcode:2006EnST...40.5962B. doi:10.1021/es060470e. PMID 17051786.

hathitrust.org

babel.hathitrust.org

Anderson, Thomas (1849). "On the constitution and properties of picoline, a new organic base from coal-tar". Transactions of the Royal Societies of Edinburgh University. 16 (2): 123–136. doi:10.1017/S0080456800024984. S2CID 100301190. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, T. (1849). "Producte der trocknen Destillation thierischer Materien" [Products of the dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 70: 32–38. doi:10.1002/jlac.18490700105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, Thomas (1851). "On the products of the destructive distillation of animal substances. Part II". Transactions of the Royal Society of Edinburgh. 20 (2): 247–260. doi:10.1017/S0080456800033160. S2CID 102143621. Archived from the original on 24 May 2020. Retrieved 24 September 2018. From p. 253: "Pyridine. The first of these bases, to which I give the name of pyridine, … "
Anderson, T. (1851). "Ueber die Producte der trocknen Destillation thierischer Materien" [On the products of dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 80: 44–65. doi:10.1002/jlac.18510800104. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Dewar, James (27 January 1871). "On the oxidation products of picoline". Chemical News. 23: 38–41. Archived from the original on 24 May 2020. Retrieved 27 September 2018.
Ladenburg, A. (1884). "Synthese des Piperidins" [Synthesis of piperidine]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 156. doi:10.1002/cber.18840170143. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ladenburg, A. (1884). "Synthese des Piperidins und seiner Homologen" [Synthesis of piperidine and its homologues]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 388–391. doi:10.1002/cber.188401701110. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ramsay, William (1876). "On picoline and its derivatives". Philosophical Magazine. 5th series. 2 (11): 269–281. doi:10.1080/14786447608639105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.

iarc.fr

monographs.iarc.fr

Pyridine (PDF). Washington DC: OSHA. 1985. Archived (PDF) from the original on 4 March 2016. Retrieved 7 January 2011. {{cite book}}: |work= ignored (help)

publications.iarc.fr

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans (2019). Some chemicals that cause tumours of the urinary tract in rodents (PDF). International Agency for Research on Cancer. Lyon, France. pp. 173–198. ISBN 978-92-832-0186-1. OCLC 1086392170. Archived (PDF) from the original on 6 May 2021. Retrieved 2 June 2021.{{cite book}}: CS1 maint: location missing publisher (link)

illinois.edu

scs.illinois.edu

Rocke, Alan J. (1988). "Koerner, Dewar and the Structure of Pyridine". Bulletin for the History of Chemistry. 2: 4. Archived from the original on 24 September 2018. Retrieved 5 May 2016.

inchem.org

"Environmental and health criteria for paraquat and diquat". Geneva: World Health Organization. 1984. Archived from the original on 6 October 2018. Retrieved 7 January 2011.
International Agency for Research on Cancer (IARC) (22 August 2000). "Pyridine Summary & Evaluation". IARC Summaries & Evaluations. IPCS INCHEM. Archived from the original on 2 October 2018. Retrieved 17 January 2007.

inrs.fr

Bonnard, N.; Brondeau, M. T.; Miraval, S.; Pillière, F.; Protois, J. C.; Schneider, O. (2011). "Pyridine" (PDF). Fiche Toxicologique (in French). INRS. Archived (PDF) from the original on 2 June 2021. Retrieved 2 June 2021.

iupac.org

Powell, W. H. (1983). "Revision of the extended Hantzsch-Widman system of nomenclature for hetero mono-cycles" (PDF). Pure and Applied Chemistry. 55 (2): 409–416. doi:10.1351/pac198855020409. S2CID 4686578. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.

nih.gov

pubmed.ncbi.nlm.nih.gov

Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Aeschbacher, HU; Wolleb, U; Löliger, J; Spadone, JC; Liardon, R (1989). "Contribution of coffee aroma constituents to the mutagenicity of coffee". Food and Chemical Toxicology. 27 (4): 227–232. doi:10.1016/0278-6915(89)90160-9. PMID 2659457.
Kostelc, J. G.; Preti, G.; Nelson, P. R.; Brauner, L.; Baehni, P. (1984). "Oral Odors in Early Experimental Gingivitis". Journal of Periodontal Research. 19 (3): 303–312. doi:10.1111/j.1600-0765.1984.tb00821.x. PMID 6235346.
Scott, T. A. (1967). "A method for the Degradation of Radioactive Nicotinic Acid". Biochemical Journal. 102 (1): 87–93. doi:10.1042/bj1020087. PMC 1270213. PMID 6030305.
Tarr, J. B.; Arditti, J. (1982). "Niacin Biosynthesis in Seedlings of Zea mays". Plant Physiology. 69 (3): 553–556. doi:10.1104/pp.69.3.553. PMC 426252. PMID 16662247.
Krygowski, T. M.; Szatyowicz, H.; Zachara, J. E. (2005). "How H-bonding Modifies Molecular Structure and π-Electron Delocalization in the Ring of Pyridine/Pyridinium Derivatives Involved in H-Bond Complexation". J. Org. Chem. 70 (22): 8859–8865. doi:10.1021/jo051354h. PMID 16238319.
Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Badger, G; Sasse, W (1963). "The Action of Metal Catalysts on Pyridines". Advances in Heterocyclic Chemistry Volume 2. Vol. 2. pp. 179–202. doi:10.1016/S0065-2725(08)60749-7. ISBN 9780120206025. PMID 14279523.
Donohoe, Timothy J.; McRiner, Andrew J.; Sheldrake, Peter (2000). "Partial Reduction of Electron-Deficient Pyridines". Organic Letters. 2 (24): 3861–3863. doi:10.1021/ol0065930. PMID 11101438.
Hawthorne, Steven B.; Sievers, Robert E. (1984). "Emissions of organic air pollutants from shale oil wastewaters". Environmental Science & Technology. 18 (6): 483–90. Bibcode:1984EnST...18..483H. doi:10.1021/es00124a016. PMID 22247953.
Stuermer, Daniel H.; Ng, Douglas J.; Morris, Clarence J. (1982). "Organic contaminants in groundwater near to underground coal gasification site in northeastern Wyoming". Environmental Science & Technology. 16 (9): 582–7. Bibcode:1982EnST...16..582S. doi:10.1021/es00103a009. PMID 22284199.
Sims, G. K.; O'Loughlin, E.J. (1992). "Riboflavin production during growth of Micrococcus luteus on pyridine". Applied and Environmental Microbiology. 58 (10): 3423–3425. Bibcode:1992ApEnM..58.3423S. doi:10.1128/AEM.58.10.3423-3425.1992. PMC 183117. PMID 16348793.
Bi, E.; Schmidt, T. C.; Haderlein, S. B. (2006). "Sorption of heterocyclic organic compounds to reference soils: column studies for process identification". Environ Sci Technol. 40 (19): 5962–5970. Bibcode:2006EnST...40.5962B. doi:10.1021/es060470e. PMID 17051786.

ncbi.nlm.nih.gov

Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Scott, T. A. (1967). "A method for the Degradation of Radioactive Nicotinic Acid". Biochemical Journal. 102 (1): 87–93. doi:10.1042/bj1020087. PMC 1270213. PMID 6030305.
Tarr, J. B.; Arditti, J. (1982). "Niacin Biosynthesis in Seedlings of Zea mays". Plant Physiology. 69 (3): 553–556. doi:10.1104/pp.69.3.553. PMC 426252. PMID 16662247.
Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Sims, G. K.; O'Loughlin, E.J. (1992). "Riboflavin production during growth of Micrococcus luteus on pyridine". Applied and Environmental Microbiology. 58 (10): 3423–3425. Bibcode:1992ApEnM..58.3423S. doi:10.1128/AEM.58.10.3423-3425.1992. PMC 183117. PMID 16348793.

orgsyn.org

Sasse, W. H. F. (1966). "2,2'-bipyridine" (PDF). Organic Syntheses. 46: 5–8. doi:10.1002/0471264180.os046.02. ISBN 0471264229. Archived from the original (PDF) on 21 January 2012.

osti.gov

Junk, G. A.; Ford, C. S. (1980). "A review of organic emissions from selected combustion processes". Chemosphere. 9 (4): 187. Bibcode:1980Chmsp...9..187J. doi:10.1016/0045-6535(80)90079-X. OSTI 5295035.

sciencemadness.org

Ladenburg, Albert. Lectures on the history of the development of chemistry since the time of Lavoisier (PDF). pp. 283–287. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.

semanticscholar.org

api.semanticscholar.org

Anderson, Thomas (1849). "On the constitution and properties of picoline, a new organic base from coal-tar". Transactions of the Royal Societies of Edinburgh University. 16 (2): 123–136. doi:10.1017/S0080456800024984. S2CID 100301190. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, Thomas (1851). "On the products of the destructive distillation of animal substances. Part II". Transactions of the Royal Society of Edinburgh. 20 (2): 247–260. doi:10.1017/S0080456800033160. S2CID 102143621. Archived from the original on 24 May 2020. Retrieved 24 September 2018. From p. 253: "Pyridine. The first of these bases, to which I give the name of pyridine, … "
Kroehnke, Fritz (1976). "The Specific Synthesis of Pyridines and Oligopyridines". Synthesis. 1976 (1): 1–24. doi:10.1055/s-1976-23941. S2CID 95238046..
Karpeiskii, Y.; Florent'ev V. L. (1969). "Condensation of Oxazoles with Dienophiles — a New Method for the Synthesis of Pyridine Bases". Russian Chemical Reviews. 38 (7): 540–546. Bibcode:1969RuCRv..38..540K. doi:10.1070/RC1969v038n07ABEH001760. S2CID 250852496.
O'Loughlin, E. J; Traina, S. J.; Sims, G. K. (2000). "Effects of sorption on the biodegradation of 2-methylpyridine in aqueous suspensions of reference clay minerals". Environmental Toxicology and Chemistry. 19 (9): 2168–2174. doi:10.1002/etc.5620190904. S2CID 98654832.
Powell, W. H. (1983). "Revision of the extended Hantzsch-Widman system of nomenclature for hetero mono-cycles" (PDF). Pure and Applied Chemistry. 55 (2): 409–416. doi:10.1351/pac198855020409. S2CID 4686578. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.

ukim.edu.mk

pmf.ukim.edu.mk

"Gattermann–Skita". Institute of Chemistry, Skopje. Archived from the original on 16 June 2006.

uni-jena.de

ipc.uni-jena.de

"Wasserbestimmung mit Karl-Fischer-Titration" [Water analysis with the Karl Fischer titration] (PDF). Jena University. Archived from the original (PDF) on 19 July 2011.

vertellus.com

"About Vertellus". vertellus.com. Archived from the original on 18 September 2012. Retrieved 7 January 2011.

web.archive.org

"Pyridine MSDS". fishersci.com. Fisher. Archived from the original on 11 June 2010. Retrieved 2 February 2010.
Pyridine (PDF). Washington DC: OSHA. 1985. Archived (PDF) from the original on 4 March 2016. Retrieved 7 January 2011. {{cite book}}: |work= ignored (help)
Anderson, Thomas (1849). "On the constitution and properties of picoline, a new organic base from coal-tar". Transactions of the Royal Societies of Edinburgh University. 16 (2): 123–136. doi:10.1017/S0080456800024984. S2CID 100301190. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, T. (1849). "Producte der trocknen Destillation thierischer Materien" [Products of the dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 70: 32–38. doi:10.1002/jlac.18490700105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Anderson, Thomas (1851). "On the products of the destructive distillation of animal substances. Part II". Transactions of the Royal Society of Edinburgh. 20 (2): 247–260. doi:10.1017/S0080456800033160. S2CID 102143621. Archived from the original on 24 May 2020. Retrieved 24 September 2018. From p. 253: "Pyridine. The first of these bases, to which I give the name of pyridine, … "
Anderson, T. (1851). "Ueber die Producte der trocknen Destillation thierischer Materien" [On the products of dry distillation of animal matter]. Annalen der Chemie und Pharmacie (in German). 80: 44–65. doi:10.1002/jlac.18510800104. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Dewar, James (27 January 1871). "On the oxidation products of picoline". Chemical News. 23: 38–41. Archived from the original on 24 May 2020. Retrieved 27 September 2018.
Rocke, Alan J. (1988). "Koerner, Dewar and the Structure of Pyridine". Bulletin for the History of Chemistry. 2: 4. Archived from the original on 24 September 2018. Retrieved 5 May 2016.
Ladenburg, Albert. Lectures on the history of the development of chemistry since the time of Lavoisier (PDF). pp. 283–287. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.
Ladenburg, A. (1884). "Synthese des Piperidins" [Synthesis of piperidine]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 156. doi:10.1002/cber.18840170143. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ladenburg, A. (1884). "Synthese des Piperidins und seiner Homologen" [Synthesis of piperidine and its homologues]. Berichte der Deutschen Chemischen Gesellschaft (in German). 17: 388–391. doi:10.1002/cber.188401701110. Archived from the original on 24 May 2020. Retrieved 15 October 2018.
Ramsay, William (1876). "On picoline and its derivatives". Philosophical Magazine. 5th series. 2 (11): 269–281. doi:10.1080/14786447608639105. Archived from the original on 24 May 2020. Retrieved 24 September 2018.
Hantzsch, A. (1881). "Condensationsprodukte aus Aldehydammoniak und ketonartigen Verbindungen" [Condensation products from aldehyde ammonia and ketone-type compounds]. Berichte der Deutschen Chemischen Gesellschaft. 14 (2): 1637–1638. doi:10.1002/cber.18810140214. Archived from the original on 22 January 2021. Retrieved 6 September 2019.
Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese" [Syntheses in the pyridine series. On an extension of the Hantzsch dihydropyridine synthesis]. Berichte der Deutschen Chemischen Gesellschaft. 31: 761–767. doi:10.1002/cber.189803101157. Archived from the original on 15 January 2020. Retrieved 29 June 2019.
Chichibabin, A. E. (1924). "Über Kondensation der Aldehyde mit Ammoniak zu Pyridinebasen" [On condensation of aldehydes with ammonia to make pyridines]. Journal für Praktische Chemie. 107: 122. doi:10.1002/prac.19241070110. Archived from the original on 20 September 2018. Retrieved 7 January 2011.
"Pyridine's Development in China". AgroChemEx. 11 May 2010. Archived from the original on 20 September 2018. Retrieved 7 January 2011.
Gattermann, L.; Skita, A. (1916). "Eine Synthese von Pyridin-Derivaten" [A synthesis of pyridine derivatives]. Chemische Berichte. 49 (1): 494–501. doi:10.1002/cber.19160490155. Archived from the original on 25 September 2020. Retrieved 29 June 2019.
"Gattermann–Skita". Institute of Chemistry, Skopje. Archived from the original on 16 June 2006.
Sasse, W. H. F. (1966). "2,2'-bipyridine" (PDF). Organic Syntheses. 46: 5–8. doi:10.1002/0471264180.os046.02. ISBN 0471264229. Archived from the original (PDF) on 21 January 2012.
"Environmental and health criteria for paraquat and diquat". Geneva: World Health Organization. 1984. Archived from the original on 6 October 2018. Retrieved 7 January 2011.
"Wasserbestimmung mit Karl-Fischer-Titration" [Water analysis with the Karl Fischer titration] (PDF). Jena University. Archived from the original (PDF) on 19 July 2011.
"Pyridine MSDS" (PDF). Alfa Aesar. Archived from the original (PDF) on 3 April 2015. Retrieved 3 June 2010.
"Database of the (EPA)". U.S. Environmental Protection Agency. Archived from the original on 18 September 2011. Retrieved 7 January 2011.
International Agency for Research on Cancer (IARC) (22 August 2000). "Pyridine Summary & Evaluation". IARC Summaries & Evaluations. IPCS INCHEM. Archived from the original on 2 October 2018. Retrieved 17 January 2007.
Bonnard, N.; Brondeau, M. T.; Miraval, S.; Pillière, F.; Protois, J. C.; Schneider, O. (2011). "Pyridine" (PDF). Fiche Toxicologique (in French). INRS. Archived (PDF) from the original on 2 June 2021. Retrieved 2 June 2021.
IARC Working Group on the Evaluation of Carcinogenic Risks to Humans (2019). Some chemicals that cause tumours of the urinary tract in rodents (PDF). International Agency for Research on Cancer. Lyon, France. pp. 173–198. ISBN 978-92-832-0186-1. OCLC 1086392170. Archived (PDF) from the original on 6 May 2021. Retrieved 2 June 2021.{{cite book}}: CS1 maint: location missing publisher (link)
"FDA Removes 7 Synthetic Flavoring Substances from Food Additives List". 5 October 2018. Archived from the original on 7 October 2018. Retrieved 8 October 2018.
Powell, W. H. (1983). "Revision of the extended Hantzsch-Widman system of nomenclature for hetero mono-cycles" (PDF). Pure and Applied Chemistry. 55 (2): 409–416. doi:10.1351/pac198855020409. S2CID 4686578. Archived (PDF) from the original on 20 September 2018. Retrieved 7 January 2011.

wiley.com

onlinelibrary.wiley.com

Ciamician, G. L.; Dennstedt, M. (1881). "Ueber die Einwirkung des Chloroforms auf die Kaliumverbindung Pyrrols". Berichte der Deutschen Chemischen Gesellschaft. 14 (1): 1153–1163. doi:10.1002/cber.188101401240. ISSN 0365-9496.

worldcat.org

Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
Ciamician, G. L.; Dennstedt, M. (1881). "Ueber die Einwirkung des Chloroforms auf die Kaliumverbindung Pyrrols". Berichte der Deutschen Chemischen Gesellschaft. 14 (1): 1153–1163. doi:10.1002/cber.188101401240. ISSN 0365-9496.
Vaganova, Evgenia; Eliaz, Dror; Shimanovich, Ulyana; Leitus, Gregory; Aqad, Emad; Lokshin, Vladimir; Khodorkovsky, Vladimir (January 2021). "Light-Induced Reactions within Poly(4-vinyl pyridine)/Pyridine Gels: The 1,6-Polyazaacetylene Oligomers Formation". Molecules. 26 (22): 6925. doi:10.3390/molecules26226925. ISSN 1420-3049. PMC 8621047. PMID 34834017.
IARC Working Group on the Evaluation of Carcinogenic Risks to Humans (2019). Some chemicals that cause tumours of the urinary tract in rodents (PDF). International Agency for Research on Cancer. Lyon, France. pp. 173–198. ISBN 978-92-832-0186-1. OCLC 1086392170. Archived (PDF) from the original on 6 May 2021. Retrieved 2 June 2021.{{cite book}}: CS1 maint: location missing publisher (link)

zenodo.org

Hantzsch, A. (1881). "Condensationsprodukte aus Aldehydammoniak und ketonartigen Verbindungen" [Condensation products from aldehyde ammonia and ketone-type compounds]. Berichte der Deutschen Chemischen Gesellschaft. 14 (2): 1637–1638. doi:10.1002/cber.18810140214. Archived from the original on 22 January 2021. Retrieved 6 September 2019.
Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese" [Syntheses in the pyridine series. On an extension of the Hantzsch dihydropyridine synthesis]. Berichte der Deutschen Chemischen Gesellschaft. 31: 761–767. doi:10.1002/cber.189803101157. Archived from the original on 15 January 2020. Retrieved 29 June 2019.
Gattermann, L.; Skita, A. (1916). "Eine Synthese von Pyridin-Derivaten" [A synthesis of pyridine derivatives]. Chemische Berichte. 49 (1): 494–501. doi:10.1002/cber.19160490155. Archived from the original on 25 September 2020. Retrieved 29 June 2019.