Rujukan Toluena

  1. ↑ "Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. m/s. 139. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. Toluene and xylene are preferred IUPAC names, but are not freely substitutable; toluene is substitutable under certain conditions, but only for general nomenclature (see P-15.1.8 for a general substitution rules for retained names). 
  2. 1 2 3 4 5 6 Templat:GESTIS
  3. 1 2 3 4 5 6 NIOSH Pocket Guide to Chemical Hazards. "#0619" (dalam bahasa Inggeris). National Institute for Occupational Safety and Health (NIOSH). 
  4. ↑ "toluene_msds". 
  5. ↑ Templat:IDLH
  6. ↑ New Environment, Inc. "New Environment Inc. - NFPA Chemicals". 
  7. ↑ McKeown, Nathanael J (Feb 1, 2015). Tarabar, Asim, penyunting. "Toluene Toxicity , Background, Pathophysiology, Epidemiology". WebMD Health Professional Network. 
  8. ↑ Devathasan, G.; Low, D.; Teoh, P. C.; Wan, S. H.; Wong, P. K. (1984). "Complications of chronic glue (toluene) abuse in adolescents". Aust N Z J Med. 14 (1): 39–43. doi:10.1111/j.1445-5994.1984.tb03583.x. PMID 6087782. 

Rujukan

WikiPedia: Toluena http://www.drugbank.ca/drugs/DB01900 http://www.chemspider.com/Chemical-Structure.1108.... http://www.jtbaker.com/msds/englishhtml/t3913.htm http://emedicine.medscape.com/article/818939-overv... http://www.newenv.com/resources/nfpa_chemicals http://chemapps.stolaf.edu/jmol/jmol.php?model=Cc1... http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=... http://pubchem.ncbi.nlm.nih.gov/summary/summary.cg... //www.ncbi.nlm.nih.gov/pubmed/6087782 http://www.kegg.jp/entry/C01455