Synonym: Ferric chloride solution, Iron(III) chloride solution
|Related Categories||1.00 g/L, AAS, AAS Concentrates, Analytical Standards, Analytical/Chromatography,|
|shelf life||(limited shelf life, expiry date on the label)|
prepared with FeCl3.6H2O, HCl and H2O
Dilute the ampule to approx. 850 mL with water. Carefully add 100 mL conc. HCl to acidify. Bring to volume with water.
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1.00 g/L, for 1L standard solution
10.00 g/L, for 1L standard solution
TraceCERT®, 1000 mg/L Fe in nitric acid
anhydrous, powder, ≥99.99% trace metals basis
reagent grade, 97%
|Precautionary statements||P273-P280-P305 + P351 + P338|
|Personal Protective Equipment||Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter|
FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: application to the total synthesis of (±)-jungianol and epi-jungianol. Dethe DH and Murhade G Org. Lett. 15(3), 429-31, (2013)
Efficient generation of ortho-naphthoquinone methides from 1,4-epoxy-1,4-dihydronaphthalenes and their annulation with allyl silanes. Sawama Y, Shishido Y, Yanase T, et al. Angew. Chem. Int. Ed. Engl. 52(5), 1515-9, (2013)
Troubleshooting the rabbit ferric chloride-induced arterial model of thrombosis to assess in vivo efficacy of antithrombotic drugs. Couture L, Richer LP, Mercier M, et al. J. Pharmacol. Toxicol. Methods 67(2), 91-7, (2013)
Intravenous ferric chloride hexahydrate supplementation induced endothelial dysfunction and increased cardiovascular risk among hemodialysis patients. Kuo KL, Hung SC, Lin YP, et al. PLoS ONE 7(12), e50295, (2012)
Changes of excitation/emission matrixes of wastewater caused by Fenton- and Fenton-like treatment and their associations with the generation of hydroxyl radicals, oxidation of effluent organic matter and degradation of trace-level organic pollutants. Li W, Nanaboina V, Zhou Q, et al. J. Hazard. Mater. 244-245, 698-708, (2013)
Tuning the reactivity of TEMPO by coordination to a Lewis acid: isolation and reactivity of MCl3(η1-TEMPO) (M = Fe, Al). Scepaniak JJ, Wright AM, Lewis RA, et al. J. Am. Chem. Soc. 134(47), 19350-3, (2012)
FeCl3-mediated Friedel-Crafts hydroarylation with electrophilic N-acetyl indoles for the synthesis of benzofuroindolines. Beaud R, Guillot R, Kouklovsky C, et al. Angew. Chem. Int. Ed. Engl. 51(50), 12546-50, (2012)
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