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Hydrochinon (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hydrochinon" in German language version.

refsWebsite
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21doi.org
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7nih.gov
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5europa.eu
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3google.de
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1dguv.de
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1reach-clp-biozid-helpdesk.de
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1suva.ch
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1archive.org
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1mpg.de
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1deutsche-apotheker-zeitung.de
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1cas.org
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archive.org

cas.org

commonchemistry.cas.org

  • National Toxicology Program: NTP Toxicology and Carcinogenesis Studies of Hydroquinone (CAS No. 123-31-9) in F344/N Rats and B6C3F1 Mice (Gavage Studies). In: National Toxicology Program Technical Report Series. Band 366, Oktober 1989, S. 1–248, PMID 12692638.

deutsche-apotheker-zeitung.de

dguv.de

gestis.dguv.de

doi.org

  • S. C. Wallwork, H. M. Powell: The crystal structure of the α form of quinol. In: J. Chem. Soc. Perkin Trans. Band 2, 1980, S. 641–646, doi:10.1039/P29800000641.
  • K. Maartmann-Moe: The crystal structure of γ-hydroquinone. In: Acta Cryst. Band 21, 1966, S. 979–982, doi:10.1107/S0365110X66004286.
  • H. Schildknecht, K. Holoubekal: Die Bombardierkäfer und ihre Explosionschemie. In: Angewandte Chemie. 73 (1), 1961, S. 1–7. doi:10.1002/ange.19610730102.
  • K. Elbs: Ueber Nitrohydrochinon. In: J. Prakt. Chem. 48, 1893, S. 179–185. doi:10.1002/prac.18930480123.
  • W. A. Caspari: The crystal structure of quinol. Part I. In: J. Chem. Soc. 1926, S. 2944–2248. doi:10.1039/JR9262902944.
  • W. A. Caspari: The crystal structure of quinol. Part II. In: J. Chem. Soc. 1927, S. 1093–1095. doi:10.1039/JR9270001093.
  • M. Naoki, T. Yoshizawa, N. Fukushima, M. Ogiso, M. Yoshino: A New Phase of Hydroquinone and Its Thermodynamic Properties. In: J. Phys. Chem. B 103, 1999, S. 6309–6313. doi:10.1021/jp990480k.
  • D. E. Palin, H. M. Powell: Hydrogen Bond Linking of Quinol Molecules. In: Nature. Band 156, 1948, S. 334. doi:10.1038/156334a0.
  • D. E. Palin, H. M. Powell: The structure of molecular compounds. Part III. Crystal structure of addition complexes of quinol with certain volatile compounds. In: J. Chem. Soc. 1947, S. 208–221. doi:10.1039/JR9470000208.
  • D. E. Palin, H. M. Powell: The structure of molecular compounds. Part VI. The β-type clathrate compounds of quinol. In: J. Chem. Soc. 1948, S. 815–821. doi:10.1039/JR9480000815.
  • M. Kohn, L. W. Guttmann: Zur Kenntnis der Bromsubstitionsprodukte des Hydrochinons. In: Monatshefte für Chemie. 45 (10), 1924, S. 573–588. doi:10.1007/BF01524599.
  • Masa-Aki Shibata, Masao Hirose, Hikaru Tanaka, Emiko Asakawa, Tomoyuki Shirai: Induction of Renal Cell Tumors in Rats and Mice, and Enhancement of Hepatocellular Tumor Development in Mice after Long-term Hydroquinone Treatment. In: Japanese Journal of Cancer Research. Band 82, Nr. 11, 1991, S. 1211–1219, doi:10.1111/j.1349-7006.1991.tb01783.x, PMID 1752780, PMC 5918322 (freier Volltext).
  • A. Barbaud, P. Modiano, M. Cocciale, S. Reichert, J.-L. Schmutz: The topical application of resorcinol can provoke a systemic allergic reaction. In: British Journal of Dermatology. Band 135, Nr. 6, 1996, S. 1014–1015, doi:10.1046/j.1365-2133.1996.d01-1121.x.
  • J. W. Pifer, F. T. Hearne, F. A. Swanson, J. L. O’Donoghue: Mortality study of employees engaged in the manufacture and use of hydroquinone. In: International Archives of Occupational and Environmental Health. Band 67, Nr. 4, 1995, S. 267–280, doi:10.1007/BF00409409, PMID 7591188.
  • Bd Carlton, H Shah: Re: "Malignant melanoma among lithographers" by H Nielsen, L Henriksen, JH Olsen. Scand J Work Environ Health 1996;22:108--11. In: Scandinavian Journal of Work, Environment & Health. Band 23, Nr. 4, August 1997, S. 308, doi:10.5271/sjweh.224.
  • U. Stenius, M. Warholm, A. Rannug, S. Walles, I. Lundberg: The role of GSH depletion and toxicity in hydroquinone-induced development of enzyme-altered foci. In: Carcinogenesis. Band 10, Nr. 3, März 1989, S. 593–599, doi:10.1093/carcin/10.3.593, PMID 2564322.
  • Junzo Suzuki, Yuichiro Inoue, Shizuo Suzuki: Changes in the urinary excretion level of 8-hydroxyguanine by exposure to reactive oxygen-generating substances. In: Free Radical Biology and Medicine. Band 18, Nr. 3, 1. März 1995, S. 431–436, doi:10.1016/0891-5849(94)00152-A.
  • G. Lévay, W. J. Bodell: Role of hydrogen peroxide in the formation of DNA adducts in HL-60 cells treated with benzene metabolites. In: Biochemical and Biophysical Research Communications. Band 222, Nr. 1, 6. Mai 1996, S. 44–49, doi:10.1006/bbrc.1996.0695, PMID 8630072.
  • G. Levay, K. Pongracz, W. J. Bodell: Detection of DNA adducts in HL-60 cells treated with hydroquinone and p-benzoquinone by 32P-postlabeling. In: Carcinogenesis. Band 12, Nr. 7, Juli 1991, S. 1181–1186, doi:10.1093/carcin/12.7.1181, PMID 2070482.
  • B. A. Hill, H. E. Kleiner, E. A. Ryan, D. M. Dulik, T. J. Monks: Identification of multi-S-substituted conjugates of hydroquinone by HPLC-coulometric electrode array analysis and mass spectroscopy. In: Chemical Research in Toxicology. Band 6, Nr. 4, Juli 1993, S. 459–469, doi:10.1021/tx00034a012, PMID 8374043.
  • Vangala V. Subrahmanyam, Prema Kolachana, Martyn T. Smith: Metabolism of hydroquinone by human myeloperoxidase: Mechanisms of stimulation by other phenolic compounds. In: Archives of Biochemistry and Biophysics. Band 286, Nr. 1, 1. April 1991, S. 76–84, doi:10.1016/0003-9861(91)90010-G.

europa.eu

echa.europa.eu

ec.europa.eu

google.de

books.google.de

mpg.de

zfn.mpdl.mpg.de

  • H. Bock, S. Nick, C. Näther, J. W. Bats: Dinatrium- und Dikalium-Nitranilate: Die Cyanin-Verzerrung der Kohlenstoff-Sechsringe. In: Zeitschrift für Naturforschung B. 49, 1994, S. 1021–1030 (PDF, freier Volltext).

nih.gov

ncbi.nlm.nih.gov

  • National Toxicology Program: NTP Toxicology and Carcinogenesis Studies of Hydroquinone (CAS No. 123-31-9) in F344/N Rats and B6C3F1 Mice (Gavage Studies). In: National Toxicology Program Technical Report Series. Band 366, Oktober 1989, S. 1–248, PMID 12692638.
  • Masa-Aki Shibata, Masao Hirose, Hikaru Tanaka, Emiko Asakawa, Tomoyuki Shirai: Induction of Renal Cell Tumors in Rats and Mice, and Enhancement of Hepatocellular Tumor Development in Mice after Long-term Hydroquinone Treatment. In: Japanese Journal of Cancer Research. Band 82, Nr. 11, 1991, S. 1211–1219, doi:10.1111/j.1349-7006.1991.tb01783.x, PMID 1752780, PMC 5918322 (freier Volltext).
  • J. W. Pifer, F. T. Hearne, F. A. Swanson, J. L. O’Donoghue: Mortality study of employees engaged in the manufacture and use of hydroquinone. In: International Archives of Occupational and Environmental Health. Band 67, Nr. 4, 1995, S. 267–280, doi:10.1007/BF00409409, PMID 7591188.
  • U. Stenius, M. Warholm, A. Rannug, S. Walles, I. Lundberg: The role of GSH depletion and toxicity in hydroquinone-induced development of enzyme-altered foci. In: Carcinogenesis. Band 10, Nr. 3, März 1989, S. 593–599, doi:10.1093/carcin/10.3.593, PMID 2564322.
  • G. Lévay, W. J. Bodell: Role of hydrogen peroxide in the formation of DNA adducts in HL-60 cells treated with benzene metabolites. In: Biochemical and Biophysical Research Communications. Band 222, Nr. 1, 6. Mai 1996, S. 44–49, doi:10.1006/bbrc.1996.0695, PMID 8630072.
  • G. Levay, K. Pongracz, W. J. Bodell: Detection of DNA adducts in HL-60 cells treated with hydroquinone and p-benzoquinone by 32P-postlabeling. In: Carcinogenesis. Band 12, Nr. 7, Juli 1991, S. 1181–1186, doi:10.1093/carcin/12.7.1181, PMID 2070482.
  • B. A. Hill, H. E. Kleiner, E. A. Ryan, D. M. Dulik, T. J. Monks: Identification of multi-S-substituted conjugates of hydroquinone by HPLC-coulometric electrode array analysis and mass spectroscopy. In: Chemical Research in Toxicology. Band 6, Nr. 4, Juli 1993, S. 459–469, doi:10.1021/tx00034a012, PMID 8374043.

reach-clp-biozid-helpdesk.de

suva.ch