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443964 Aldrich

Lithium iodate

97%

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Description

Packaging

100 g in poly bottle

Price and Availability


Ultra-high Purity Salts

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Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Hazard Codes (Europe) 
O,T
Risk Statements (Europe) 
Safety Statements (Europe) 
53-17-22-36/37/39-45
RIDADR 
UN 1479 5.1 / PGII
WGK Germany 
3

Documents

Certificate of Analysis

Certificate of Origin

Protocols & Articles

Peer-Reviewed Papers

References

Set your institution to view full text papers.

Colour reactions of iodic acid as reagent for identifying drugs by thin-layer chromatography. Cavazzutti G, Gagliardi L, Amato A, et al. J. Chromatogr. A 268(3), 528-34, (1983)

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[Correlation between ERPF and retention function on 131I-OIH renogram]. Maeda M, Hasegawa R, and Yoshida H Kaku Igaku. 21(10), 1285-92, (1984)

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Multiwalled carbon nanotubes dispersed in carminic acid for the development of catalase based biosensor for selective amperometric determination of H(2)O(2) and iodate. Periasamy AP, Ho YH, and Chen SM Biosens. Bioelectron. 29(1), 151-8, (2011)

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Accounting for changes in particle charge, dry mass and composition occurring during studies of single levitated particles. Haddrell AE, Davies JF, Yabushita A, et al. J. Phys. Chem. A 116(40), 9941-53, (2012)

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A novel synthesis of 3,5-diiodotyrosine with iodic acid. Liu W, Zhou J, and Wong JT Anal. Biochem. 120(1), 204-7, (1982)

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Structural characterization of the first hydroxo-bridged plutonium compound, (PuO(2))(2)(IO(3))(mu(2)-OH)(3). Bean AC, Abney K, Scott BL, et al. Inorg. Chem. 44(15), 5209-11, (2005)

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Determination of some aminobenzoic acid derivatives: glafenine and metoclopramide. Moussa BA J. Pharm. Biomed. Anal. 23(6), 1045-55, (2000)

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Reactive liposomes encapsulating a glucose oxidase-peroxidase system with antibacterial activity. Hill KJ, Kaszuba M, Creeth JE, et al. Biochim. Biophys. Acta 1326(1), 37-46, (1997)

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Oxidative stress of human erythrocytes by iodate and periodate. Reversible formation of aqueous membrane pores due to SH-group oxidation. Heller KB, Poser B, Haest CW, et al. Biochim. Biophys. Acta 777(1), 107-16, (1984)

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An aromatic iodination method, with iodic acid used as the only iodinating reagent. Krassowska-Swiebocka B, Prokopienko G, and Skulski L Molecules 10(2), 394-400, (2005)

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