Ditionito de sodio (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ditionito de sodio" in Spanish language version.

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125px.com

«Kodak Direct Positive Film 5246». 125px.com. Kodak. Consultado el 6 de noviembre de 2019.

acs.org

pubs.acs.org

J. Org. Chem., 1980, 45 (21), pp 4126–4129, http://pubs.acs.org/doi/abs/10.1021/jo01309a011

archive.org

Catherine E. Housecroft; Alan G. Sharpe (2008). «Chapter 16: The group 16 elements». Inorganic Chemistry, 3rd Edition. Pearson. p. 520. ISBN 978-0-13-175553-6.

doi.org

dx.doi.org

Weinrach, J. B.; Meyer, D. R.; Guy, J. T.; Michalski, P. E.; Carter, K. L.; Grubisha, D. S.; Bennett, D. W. (1992). «A structural study of sodium dithionite and its ephemeral dihydrate: A new conformation for the dithionite ion». Journal of Crystallographic and Spectroscopic Research 22 (3): 291-301. doi:10.1007/BF01199531.
José Jiménez Barberá; Adolf Metzger; Manfred Wolf (15 de junio de 2000). «Sulfites, Thiosulfates, and Dithionites». Ullmann's Encyclopedia of Industrial Chemistry. Wiley Online Library. ISBN 978-3527306732. doi:10.1002/14356007.a25_477.
Mayhew, S. G. (2008). «The Redox Potential of Dithionite and SO−2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase». European Journal of Biochemistry 85 (2): 535-547. PMID 648533. doi:10.1111/j.1432-1033.1978.tb12269.x.
Božič, Mojca; Kokol, Vanja (2008). «Ecological alternatives to the reduction and oxidation processes in dyeing with vat and sulphur dyes». Dyes and Pigments 76 (2): 299-309. doi:10.1016/j.dyepig.2006.05.041.
MAYHEW, Stephen G. (1978). «The Redox Potential of Dithionite and SO-2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase». European Journal of Biochemistry 85 (2): 535-547. ISSN 0014-2956. PMID 648533. doi:10.1111/j.1432-1033.1978.tb12269.x.
Kenneth L. Williamson "Reduction of Indigo: Sodium Hydrosulfite as a Reducing Agent" J. Chem. Educ., 1989, volume 66, p 359. doi 10.1021/ed066p359.2
Knight, David W. (15 de septiembre de 2006). 1-Hydroxypyridine-2(1H)-thione. «1-Hydroxypyridine-2(1H)-thione». Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. ISBN 978-0471936237. doi:10.1002/047084289X.rh067.pub2.

inchem.org

«Sodium dithionite - ipcs inchem». www.inchem.org. Berliln, Germany. 2004. Archivado desde el original el 17 de abril de 2018. Consultado el 15 de junio de 2018.

issn.org

portal.issn.org

MAYHEW, Stephen G. (1978). «The Redox Potential of Dithionite and SO-2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase». European Journal of Biochemistry 85 (2): 535-547. ISSN 0014-2956. PMID 648533. doi:10.1111/j.1432-1033.1978.tb12269.x.

nih.gov

ncbi.nlm.nih.gov

Mayhew, S. G. (2008). «The Redox Potential of Dithionite and SO−2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase». European Journal of Biochemistry 85 (2): 535-547. PMID 648533. doi:10.1111/j.1432-1033.1978.tb12269.x.
MAYHEW, Stephen G. (1978). «The Redox Potential of Dithionite and SO-2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase». European Journal of Biochemistry 85 (2): 535-547. ISSN 0014-2956. PMID 648533. doi:10.1111/j.1432-1033.1978.tb12269.x.

nist.gov

webbook.nist.gov

Número CAS

patents.google.com

«Aldehyde sulfoxylate systemic fungicides». google.com. Archivado desde el original el 27 de abril de 2018. Consultado el 27 de abril de 2018.

web.archive.org

«Aldehyde sulfoxylate systemic fungicides». google.com. Archivado desde el original el 27 de abril de 2018. Consultado el 27 de abril de 2018.
«Sodium dithionite - ipcs inchem». www.inchem.org. Berliln, Germany. 2004. Archivado desde el original el 17 de abril de 2018. Consultado el 15 de junio de 2018.