Hidroquinona (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hidroquinona" in Galician language version.

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12doi.org

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8nih.gov

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6docs.google.com

1,047^th place

632^nd place

5web.archive.org

1^st place

5worldcat.org

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2cdc.gov

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2fda.gov

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2archive.org

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1inchem.org

4,334^th place

1,590^th place

1hathitrust.org

441^st place

975^th place

1researchgate.net

120^th place

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1europa.eu

68^th place

75^th place

1beskinformed.com

low place

1jdsupra.com

low place

1safecosmetics.org

low place

1books.google.com

3^rd place

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archive.org

Olumide, YM; Akinkugbe, AO; Altraide, D; Mohammed, T; Ahamefule, N; Ayanlowo, S; Onyekonwu, C; Essen, N (abril de 2008). "Complications of chronic use of skin lightening cosmetics". International Journal of Dermatology 47 (4): 344–53. PMID 18377596. doi:10.1111/j.1365-4632.2008.02719.x.
Burdock, G.A. (1998). "Review of the biological properties and toxicity of bee propolis (propolis)". Food and Chemical Toxicology 36 (4): 347–363. PMID 9651052. doi:10.1016/S0278-6915(97)00145-2.

beskinformed.com

"Clear N Smooth Skin Toning Cream recalled". 2011-10-04. Consultado o 4 de abril de 2018.

books.google.com

The Beaver: Its Life and Impact. Dietland Muller-Schwarze, 2003, page 43 (libro en Google books)

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0338". National Institute for Occupational Safety and Health (NIOSH).
"Hydroquinone". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).

docs.google.com

Hubel, Karl; Braye, Henri (1960). Process for the preparation of substituted cyclic compounds and products resulting therefrom US3149138 A (PDF). Union Carbide Corp.
Pino, Piero; Braca, Giuseppe; Sbrana, Glauco (1964). Preparation of hydroquinone US3355503 A (PDF). Lonza Ag.
Walter, Reppe; Magin, August (1966). Production of hydroquinones US3394193 A (PDF). Basf Ag.
Piero, Pino; Giuseppe, Braca; Frediano, Settimo; Glauco, Sbrana (1967). Preparation of hydroquinone US3459812 A (PDF). Lonza Ag.
Holmes, J.; Hagemeyer, H. (1971). Process for the production of hydroquinone US 3742071 A (PDF). Eastman Kodak Co.
Holmes, J.; Hagemeyer, H. (1971). Process for the production of hydroquinone US 3742071 A (PDF). Eastman Kodak Co.

doi.org

dx.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. ISBN 978-0-85404-182-4. doi:10.1039/9781849733069-FP001.
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.
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.
Olumide, YM; Akinkugbe, AO; Altraide, D; Mohammed, T; Ahamefule, N; Ayanlowo, S; Onyekonwu, C; Essen, N (abril de 2008). "Complications of chronic use of skin lightening cosmetics". International Journal of Dermatology 47 (4): 344–53. PMID 18377596. doi:10.1111/j.1365-4632.2008.02719.x.
Draelos, Zoe Diana (2007-09-01). "Skin lightening preparations and the hydroquinone controversy". Dermatologic Therapy 20 (5): 308–313. ISSN 1529-8019. PMID 18045355. doi:10.1111/j.1529-8019.2007.00144.x.
Bandyopadhyay, Debabrata (2009-01-01). "Topical treatment of melasma". Indian Journal of Dermatology 54 (4): 303–309. ISSN 0019-5154. PMC 2807702. PMID 20101327. doi:10.4103/0019-5154.57602.
Mazurek, Klaudia; Pierzchała, Ewa (2016-09-01). "Comparison of efficacy of products containing azelaic acid in melasma treatment". Journal of Cosmetic Dermatology 15 (3): 269–282. ISSN 1473-2165. PMID 27028014. doi:10.1111/jocd.12217.
Mansouri, P.; Farshi, S.; Hashemi, Z.; Kasraee, B. (2015-07-01). "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. ISSN 1365-2133. PMID 25251767. doi:10.1111/bjd.13424.
Joval, E; Kroeger, P; N (abril de 1996). "Hydroquinone: the toxic compound of Agaricus hondensis". Planta Medica 62 (2): 185. PMID 17252436. doi:10.1055/s-2006-957852.
Burdock, G.A. (1998). "Review of the biological properties and toxicity of bee propolis (propolis)". Food and Chemical Toxicology 36 (4): 347–363. PMID 9651052. doi:10.1016/S0278-6915(97)00145-2.

europa.eu

eur-lex.europa.eu

76/768/EEC:1976 Council Directive 76/768/EEC of 27 de xullo de 1976 on the approximation of the laws of the Member States relating to cosmetic products : http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CELEX:31976L0768:EN:HTML

fda.gov

United States Food and Drug Administration (2006). Skin Bleaching Drug Products for Over-the-Counter Product Use; Proposed Rule (PDF) (Informe). 1978N-0065. Arquivado dende o orixinal (PDF) o 2011-05-16.
Research, Center for Drug Evaluation and. "About the Center for Drug Evaluation and Research - Hydroquinone Studies Under The National Toxicology Program (NTP)". www.fda.gov (en inglés). Arquivado dende o orixinal o 2017-01-22. Consultado o 2017-02-12.

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." (O destilado así obtido … contén … unha nova substancia cristalizable que describirei, co nome hidroquinona incolora, máis abaixo en maior detalle.) [Nota: a fórmula empírica de Wöhler para a hidroquinona (p. 152) é incorrecta porque (1) el atribuíulle á molécula 25 (en vez de 24) átomos de carbono, e (2) como facían moitos químicos daquel tempo, usaba masas atómicas incorrectas para o carbono (6 en vez de 12) e o oxíxeno (8 en vez de 16). Con estas correccións, a súa fórmula empírica queda así: C₁₂H₁₂O₄. Dividindo os subíndices por 2, o resultado é: C₆H₆O₂, que é correcto.]

inchem.org

"Hydroquinone" (PDF). OECD SIDS. UNEP Publications. Arquivado dende o orixinal (PDF) o 2016-10-20. Consultado o 2018-09-17.

jdsupra.com

"Congress Enacts OTC Monograph Reform". JD Supra (en inglés). Consultado o 2021-12-19.

nih.gov

ncbi.nlm.nih.gov

Olumide, YM; Akinkugbe, AO; Altraide, D; Mohammed, T; Ahamefule, N; Ayanlowo, S; Onyekonwu, C; Essen, N (abril de 2008). "Complications of chronic use of skin lightening cosmetics". International Journal of Dermatology 47 (4): 344–53. PMID 18377596. doi:10.1111/j.1365-4632.2008.02719.x.
Draelos, Zoe Diana (2007-09-01). "Skin lightening preparations and the hydroquinone controversy". Dermatologic Therapy 20 (5): 308–313. ISSN 1529-8019. PMID 18045355. doi:10.1111/j.1529-8019.2007.00144.x.
Bandyopadhyay, Debabrata (2009-01-01). "Topical treatment of melasma". Indian Journal of Dermatology 54 (4): 303–309. ISSN 0019-5154. PMC 2807702. PMID 20101327. doi:10.4103/0019-5154.57602.
Mazurek, Klaudia; Pierzchała, Ewa (2016-09-01). "Comparison of efficacy of products containing azelaic acid in melasma treatment". Journal of Cosmetic Dermatology 15 (3): 269–282. ISSN 1473-2165. PMID 27028014. doi:10.1111/jocd.12217.
Mansouri, P.; Farshi, S.; Hashemi, Z.; Kasraee, B. (2015-07-01). "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. ISSN 1365-2133. PMID 25251767. doi:10.1111/bjd.13424.
Joval, E; Kroeger, P; N (abril de 1996). "Hydroquinone: the toxic compound of Agaricus hondensis". Planta Medica 62 (2): 185. PMID 17252436. doi:10.1055/s-2006-957852.
Burdock, G.A. (1998). "Review of the biological properties and toxicity of bee propolis (propolis)". Food and Chemical Toxicology 36 (4): 347–363. PMID 9651052. doi:10.1016/S0278-6915(97)00145-2.

ntp.niehs.nih.gov

"Hydroquinone 10022-H". ntp.niehs.nih.gov (en inglés). Arquivado dende o orixinal o 2017-10-01. Consultado o 2017-02-12.

researchgate.net

Additive manufacturing of ceramics from preceramic polymers Additive manufacturing 2019 vol. 27. pp 80-90

safecosmetics.org

Campaign For Safe Cosmetics - Hydroquinone Arquivado 2010-11-27 en Wayback Machine.

web.archive.org

"Hydroquinone" (PDF). OECD SIDS. UNEP Publications. Arquivado dende o orixinal (PDF) o 2016-10-20. Consultado o 2018-09-17.
United States Food and Drug Administration (2006). Skin Bleaching Drug Products for Over-the-Counter Product Use; Proposed Rule (PDF) (Informe). 1978N-0065. Arquivado dende o orixinal (PDF) o 2011-05-16.
Research, Center for Drug Evaluation and. "About the Center for Drug Evaluation and Research - Hydroquinone Studies Under The National Toxicology Program (NTP)". www.fda.gov (en inglés). Arquivado dende o orixinal o 2017-01-22. Consultado o 2017-02-12.
Campaign For Safe Cosmetics - Hydroquinone Arquivado 2010-11-27 en Wayback Machine.
"Hydroquinone 10022-H". ntp.niehs.nih.gov (en inglés). Arquivado dende o orixinal o 2017-10-01. Consultado o 2017-02-12.

worldcat.org

Streitwieser, Andrew (1992). Introduction to organic chemistry. Heathcock, Clayton H., 1936-, Kosower, Edward M. (4th ed.). Upper Saddle River, N.J.: Prentice Hall. ISBN 978-0139738500. OCLC 52836313.
Draelos, Zoe Diana (2007-09-01). "Skin lightening preparations and the hydroquinone controversy". Dermatologic Therapy 20 (5): 308–313. ISSN 1529-8019. PMID 18045355. doi:10.1111/j.1529-8019.2007.00144.x.
Bandyopadhyay, Debabrata (2009-01-01). "Topical treatment of melasma". Indian Journal of Dermatology 54 (4): 303–309. ISSN 0019-5154. PMC 2807702. PMID 20101327. doi:10.4103/0019-5154.57602.
Mazurek, Klaudia; Pierzchała, Ewa (2016-09-01). "Comparison of efficacy of products containing azelaic acid in melasma treatment". Journal of Cosmetic Dermatology 15 (3): 269–282. ISSN 1473-2165. PMID 27028014. doi:10.1111/jocd.12217.
Mansouri, P.; Farshi, S.; Hashemi, Z.; Kasraee, B. (2015-07-01). "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. ISSN 1365-2133. PMID 25251767. doi:10.1111/bjd.13424.