Tham khảo Axetandehit

  1. Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. tr. 908. ISBN 978-0-85404-182-4. doi:10.1039/9781849733069-FP001
  2. SciFinderScholar (accessed 4 Nov 2009). Acetaldehyde (75-07-0) Substance Detail.
  3. Molecular Pathology and Diagnostics of Cancer p.190
  4. 1 2 Stoffdaten Acetaldehyd bei Celanese Chemicals. as of December 1999.
  5. 1 2 3 “NIOSH Pocket Guide to Chemical Hazards #0001”. Viện An toàn và Sức khỏe Nghề nghiệp Quốc gia Hoa Kỳ (NIOSH). 
  6. https://pubchem.ncbi.nlm.nih.gov/compound/formaldehyde#section=Odor-Threshold
  7. “Acidity of aldehydes”. Truy cập 4 tháng 12 năm 2017. 
  8. 1 2 “Acetaldehyde”. NIOSH. Ngày 4 tháng 12 năm 2014. Truy cập ngày 12 tháng 2 năm 2015. 
  9. 1 2 3 Bản dữ liệu Axetandehit của Sigma-Aldrich, truy cập lúc {{{Datum}}} (PDF).Vorlage:Sigma-Aldrich/Vorlagenfehler
  10. Uebelacker, Michael; Lachenmeier, Dirk (ngày 13 tháng 6 năm 2011). “Quantitative Determination of Acetaldehyde in Foods Using Automated Digestion with Simulated Gastric Fluid Followed by Headspace Gas Chromatography”. Journal of Automated Methods and Management in Chemistry. PMC 3124883
  11. “Chemicals in the Environment: Acetaldehyde (CAS NO. 75-07-0)]. Office of Pollution Prevention and Toxics”. epa.gov. United States Environmental Protection Agency. Tháng 8 năm 1994. 
  12. List of IARC Group 1 carcinogens
  13. Zhou, Ying; Li, Chaoyang; Huijbregts, Mark A. J.; Mumtaz, M. Moiz (ngày 7 tháng 10 năm 2015). “Carcinogenic Air Toxics Exposure and Their Cancer-Related Health Impacts in the United States”. PLoS One 10 (10): e0140013. PMC 4596837. PMID 26444872. doi:10.1371/journal.pone.0140013
  14. Scheele, C. W. (1774) "Om Brunsten eller Magnesia nigra och dess egenskaper" (On brown-stone or black magnesia [i.e., manganese ore] and its properties), Kungliga Svenska vetenskapsakademiens handlingar (Proceedings of the Royal Swedish Academy of Sciences), 35: 89–116; 177–194. On pages 109–110, Scheele mentions that refluxing ("digesting") ethanol (Alkohol vini) with manganese dioxide (Brunsten) and either hydrochloric acid (Spirtus salis) or sulfuric acid (Spiritus Vitrioli) produces a smell like "Aether nitri" (ethanol treated with nitric acid). Later investigators realized that Scheele had produced acetaldehyde.
  15. Note:
  16. See:
  17. Liebig, Justus (1835) "Ueber die Producte der Oxydation des Alkohols" (On the products of oxidation of alcohol [i.e., ethanol]), Annalen der Chemie, 14: 133–167.
  18. Brock, William H. (1997) Justus von Liebig: The Chemical Gatekeeper. Cambridge, England: Cambridge University Press, pp. 83–84.
  19. Liebig, J. (1835) "Sur les produits de l'oxidation de l'alcool" (On the products of the oxidation of alcohol), Annales de Chimie et de Physique, 59: 289–327. From p. 290: "Je le décrirai dans ce mémoire sous le nom d'aldehyde; ce nom est formé de alcool dehydrogenatus." (I will describe it in this memoir by the name of aldehyde; this name is formed from alcohol dehydrogenatus.)
  20. The name change occurred at least as early as 1868. See, for example: Eugen F. von Gorup-Besanez, ed., Lehrbuch der organischen Chemie für den Unterricht auf Universitäten … [Textbook of Organic Chemistry for Instruction at Universities …], 3rd ed. (Braunschweig, Germany: Friedrich Vieweg und Sohn, 1868), vol. 2, p. 88.

Tài liệu tham khảo

WikiPedia: Axetandehit http://www.chemvip.com/eurprodbull-acetaldehyde-de... http://www.inclusive-science-engineering.com/aceta... http://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSP... http://www.sigmaaldrich.com/catalog/search/Product... http://chemistry.stackexchange.com/questions/12232... http://www.indiana.edu/~rcapub/v17n3/p18.html http://chemapps.stolaf.edu/jmol/jmol.php?model=CC%... http://chemapps.stolaf.edu/jmol/jmol.php?model=O%3... http://monographs.iarc.fr/ENG/Monographs/vol71/ind... http://www.epa.gov/chemfact/f_acetal.txt