Hydroquinone (English Wikipedia)

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

refsWebsite
Global rank English rank
2nd place
2nd place
4th place
4th place
1st place
1st place
11th place
8th place
1,047th place
1,015th place
5th place
5th place
218th place
212th place
3,912th place
2,496th place
447th place
338th place
4,334th place
4,154th place
low place
low place
441st place
311th place
120th place
125th place
68th place
117th place
low place
low place
low place
low place
low place
low place
3rd place
3rd place

beskinformed.com

books.google.com

cdc.gov

clincalc.com

docs.google.com

doi.org

  • "Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 691. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  • Lander, John J.; Svirbely, John J. Lander, W. J. (1945). "The Dipole Moments of Catechol, Resorcinol and Hydroquinone". Journal of the American Chemical Society. 67 (2): 322–324. doi:10.1021/ja01218a051.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Phillip M. Hudnall "Hydroquinone" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. 2005 Wiley-VCH, Weinheim. doi:10.1002/14356007.a13_499.
  • Gerhard Franz, Roger A. Sheldon "Oxidation" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2000 doi:10.1002/14356007.a18_261
  • Reppe, Walter; Kutepow, N; Magin, A (1969). "Cyclization of Acetylenic Compounds". Angewandte Chemie International Edition in English. 8 (10): 727–733. doi:10.1002/anie.196907271.
  • Shi Y, Xia Y, Xu G, Wen L, Gao G, Zong B (28 October 2021). "Hydrogen peroxide and applications in green hydrocarbon nitridation and oxidation". Chinese Journal of Chemical Engineering (Review article). 41: 145–161. doi:10.1016/j.cjche.2021.09.030. S2CID 240248911.
  • Shi Y, Xia Y, Xu G, Wen L, Gao G, Zong B (28 October 2021). "Hydrogen peroxide and applications in green hydrocarbon nitridation and oxidation". Chinese Journal of Chemical Engineering (Review article). 41: 145–161. doi:10.1016/j.cjche.2021.09.030. S2CID 240248911.
  • Olumide, YM; Akinkugbe, AO; Altraide, D; Mohammed, T; Ahamefule, N; Ayanlowo, S; Onyekonwu, C; Essen, N (April 2008). "Complications of chronic use of skin lightening cosmetics". International Journal of Dermatology. 47 (4): 344–53. doi:10.1111/j.1365-4632.2008.02719.x. PMID 18377596. S2CID 8159382.
  • Draelos, Zoe Diana (1 September 2007). "Skin lightening preparations and the hydroquinone controversy". Dermatologic Therapy. 20 (5): 308–313. doi:10.1111/j.1529-8019.2007.00144.x. ISSN 1529-8019. PMID 18045355. S2CID 24913995.
  • Bandyopadhyay, Debabrata (1 January 2009). "Topical treatment of melasma". Indian Journal of Dermatology. 54 (4): 303–309. doi:10.4103/0019-5154.57602. ISSN 0019-5154. PMC 2807702. PMID 20101327.
  • Mazurek, Klaudia; Pierzchała, Ewa (1 September 2016). "Comparison of efficacy of products containing azelaic acid in melasma treatment". Journal of Cosmetic Dermatology. 15 (3): 269–282. doi:10.1111/jocd.12217. ISSN 1473-2165. PMID 27028014. S2CID 25303091.
  • Mansouri, P.; Farshi, S.; Hashemi, Z.; Kasraee, B. (1 July 2015). "Evaluation of the efficacy of cysteamine 5% cream in the treatment of epidermal melasma: a randomized double-blind placebo-controlled trial". The British Journal of Dermatology. 173 (1): 209–217. doi:10.1111/bjd.13424. ISSN 1365-2133. PMID 25251767. S2CID 21618233.
  • Joval, E; Kroeger, P; N (April 1996). "Hydroquinone: the toxic compound of Agaricus hondensis". Planta Medica. 62 (2): 185. doi:10.1055/s-2006-957852. PMID 17252436. S2CID 260249338.
  • Burdock, G.A. (1998). "Review of the biological properties and toxicity of bee propolis (propolis)". Food and Chemical Toxicology. 36 (4): 347–363. doi:10.1016/S0278-6915(97)00145-2. PMID 9651052.

europa.eu

eur-lex.europa.eu

fda.gov

hathitrust.org

babel.hathitrust.org

  • F. Wöhler (1844) "Untersuchungen über das Chinon" (Investigations of quinone), Annalen der Chemie und Pharmacie, 51 : 145-163. From page 146: "Das so erhaltene Destillat … enthält … einen neuen, krystallisierenden Körper, den ich unter dem Namen farbloses Hydrochinon weiter unten näher beschreiben werde." (The distillate so obtained … contains … a new, crystallizable substance, that I will describe, under the name of colorless hydroquinone, further below in more detail.) [Note: Wöhler's empirical formula for hydroquinone (p. 152) is incorrect because (1) he attributed 25 (instead of 24) carbon atoms to the molecule, and (2) as many chemists at the time did, he used the wrong atomic masses for carbon (6 instead of 12) and oxygen (8 instead of 16). With these corrections, his empirical formula becomes: C12H12O4. Dividing the subscripts by 2, the result is: C6H6O2, which is correct.]

inchem.org

jdsupra.com

nih.gov

pubmed.ncbi.nlm.nih.gov

ntp.niehs.nih.gov

ncbi.nlm.nih.gov

openstudy.com

assets.openstudy.com

researchgate.net

safecosmetics.org

semanticscholar.org

api.semanticscholar.org

web.archive.org

worldcat.org

search.worldcat.org