Adipic acid (English Wikipedia)

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

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acs.org

American Chemical Society (9 February 2015). "Molecule of the Week: Adipic Acid".

books.google.com

Ince, Walter (1895). "Preparation of adipic acid and some of its derivatives". Journal of the Chemical Society, Transactions. 67: 155–159. doi:10.1039/CT8956700155.

doi.org

Mac Gillavry, C. H. (2010). "The crystal structure of adipic acid". Recueil des Travaux Chimiques des Pays-Bas. 60 (8): 605–617. doi:10.1002/recl.19410600805.
Musser, M. T. (2005). "Adipic Acid". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_269. ISBN 3527306730.
Parmon, V. N.; Panov, G. I.; Uriarte, A.; Noskov, A. S. (2005). "Nitrous oxide in oxidation chemistry and catalysis application and production". Catalysis Today. 100 (2005): 115–131. doi:10.1016/j.cattod.2004.12.012.
Sato, K.; Aoki, M.; Noyori, R. (1998). "A "Green" route to adipic acid: direct oxidation of cyclohexenes with 30 percent hydrogen peroxide". Science. 281 (5383): 1646–47. Bibcode:1998Sci...281.1646S. doi:10.1126/science.281.5383.1646. PMID 9733504.
Ince, Walter (1895). "Preparation of adipic acid and some of its derivatives". Journal of the Chemical Society, Transactions. 67: 155–159. doi:10.1039/CT8956700155.
Cornils, Boy; Lappe, Peter (2000). "Dicarboxylic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_523. ISBN 978-3527306732.
Reimer, R. A.; Slaten, C. S.; Seapan, M.; Koch, T. A.; Triner, V. G. (2000). "Adipic Acid Industry — N₂O Abatement". Non-CO₂ Greenhouse Gases: Scientific Understanding, Control and Implementation. Netherlands: Springer. pp. 347–358. doi:10.1007/978-94-015-9343-4_56. ISBN 978-94-015-9343-4.

epa.gov

US EPA (12 August 2013). "U.S. Greenhouse Gas Inventory Report, Chapter 4. Industrial Processes" (PDF). Retrieved 2013-11-29.

harvard.edu

ui.adsabs.harvard.edu

Sato, K.; Aoki, M.; Noyori, R. (1998). "A "Green" route to adipic acid: direct oxidation of cyclohexenes with 30 percent hydrogen peroxide". Science. 281 (5383): 1646–47. Bibcode:1998Sci...281.1646S. doi:10.1126/science.281.5383.1646. PMID 9733504.

kraftbrands.com

"Cherry Jell-O Nutrition Facts". Kraft Foods. Archived from the original on 24 September 2019. Retrieved 21 Mar 2012.

nih.gov

pubmed.ncbi.nlm.nih.gov

Sato, K.; Aoki, M.; Noyori, R. (1998). "A "Green" route to adipic acid: direct oxidation of cyclohexenes with 30 percent hydrogen peroxide". Science. 281 (5383): 1646–47. Bibcode:1998Sci...281.1646S. doi:10.1126/science.281.5383.1646. PMID 9733504.

orgsyn.org

Ellis, B. A. (1925). "Adipic Acid". Organic Syntheses. 5: 9; Collected Volumes, vol. 1, p. 560.
Thorpe, J. F.; Kon, G. A. R. (1925). "Cyclopentanone". Organic Syntheses. 5: 37; Collected Volumes, vol. 1, p. 192.

pcinylon.com

"Adipic Acid". Archived from the original on 2015-05-18. Retrieved 2015-05-09. PCI abstract for adipic acid

rsc.org

"Adipic Acid". The Merck Index. Royal Society of Chemistry. 2013. Retrieved 2 March 2017.

sciencedirect.com

"Polyvinylchloride - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2023-11-10.

web.archive.org

"Adipic Acid". Archived from the original on 2015-05-18. Retrieved 2015-05-09. PCI abstract for adipic acid
"Cherry Jell-O Nutrition Facts". Kraft Foods. Archived from the original on 24 September 2019. Retrieved 21 Mar 2012.