Rujukan Fenol

  1. ↑ "Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. m/s. 690. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. Only one name is retained, phenol, for C6H5-OH, both as a preferred name and for general nomenclature. 
  2. ↑ "Phenol_msds". 
  3. 1 2 3 4 5 NIOSH Pocket Guide to Chemical Hazards. "#0493" (dalam bahasa Inggeris). National Institute for Occupational Safety and Health (NIOSH). 
  4. ↑ Kütt, Agnes; Movchun, Valeria; Rodima, Toomas; Dansauer, Timo; Rusanov, Eduard B.; Leito, Ivo; Kaljurand, Ivari; Koppel, Juta; Pihl, Viljar; Koppel, Ivar; Ovsjannikov, Gea; Toom, Lauri; Mishima, Masaaki; Medebielle, Maurice; Lork, Enno; Röschenthaler, Gerd-Volker; Koppel, Ilmar A.; Kolomeitsev, Alexander A. (2008). "Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline". The Journal of Organic Chemistry. 73 (7): 2607–20. doi:10.1021/jo702513w. PMID 18324831. 
  5. ↑ http://omlc.ogi.edu/spectra/PhotochemCAD/html/phenol.html
  6. 1 2 3 Templat:Sigma-Aldrich
  7. 1 2 Templat:IDLH
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Rujukan

WikiPedia: Fenol http://www.drugbank.ca/drugs/DB03255 http://www.chemblink.com/MSDS/MSDSFiles/108-95-2_S... http://www.chemspider.com/Chemical-Structure.971.h... http://omlc.ogi.edu/spectra/PhotochemCAD/html/phen... http://chemapps.stolaf.edu/jmol/jmol.php?model=c1c... http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=... http://pubchem.ncbi.nlm.nih.gov/summary/summary.cg... //www.ncbi.nlm.nih.gov/pubmed/18324831 http://www.kegg.jp/entry/D06536 http://www.commonchemistry.org/ChemicalDetail.aspx...