10294-54-9O=S(=O)([O-])[O-].[Cs+].[Cs+]FLJPGEWQYJVDPF-UHFFFAOYSA-Lused in forming density gradients
10294-54-9DTXSID10883109Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
This chemical does not meet GHS hazard criteria for 18.5% (33 of 178) of reports.
Warning
H302 (81.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P203, P260, P264, P270, P280, P301+P317, P318, P319, P330, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 178 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Chemical: Sulfuric acid, dicesium salt
REACH registered substance: Caesium sulphate (EC: 233-662-6)
Sulfuric acid, dicaesium salt: Does not have an individual approval but may be used under an appropriate group standard
DescriptionCesium sulfate is used for equilibrium density gradient centrifugation, one of the most useful tools for fractionation and characterization of macromolecules, such as DNA. Cesium sulfate can be used as catalyst, e.g. catalyst of cesium sulfate/vanadium pentoxide is used in abiabatic multibed reactors to lower inlet temperature and catalyst cesium sulfate/zeolite is used in a pilot plant scale process to synthesize 4-methyl thiazol.
UsesCesium sulfate is used to prepare dense aqueous solutions for use in isopycnic centrifugation. It is also used for crystal growing purposes.
UsesCesium sulfate is the basic raw material for the preparation of various cesium salts, and can be used in trace analysis of aluminum and berkelium analysis reagent. It is often used as a liquid medium for density gradient centrifugation to separate and extract nucleic acids, suborganelles and plasmids [4].
UsesWith V or V2O5 as catalyst for SO2 oxidation.
PreparationLepidolite is an important mineral resource for the preparation of lithium, rubidium and cesium[5]. And cesium can be collected from the leaching solution by the process of crystallization, roasting, dissolution and solvent extraction. After the leaching solution is cooled from 85 °C to 35 °C. The mixture is calcined at 900 °C after most of Cs+ is precipitated as CsAl(SO4)2.XH2O, and the calcined product is dissolved in water to obtain Cs+ mixed sulfuric acid solution[6]. After four-stage countercurrent extraction, obtain the mixed sulfuric acid solutionis. Cs+ (99.20%) was extracted and purified by 4-tert-butyl-2-(α-methylbenzyl) phenol (t-BAMBP). The organic phase dissolved with CS+ was scrubbing and stripped with sulfuric acid, and cesium sulfate products were obtained after crystallization.
No reaction records under the current filter.
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