推薦產品
化驗
≥99%
反應適用性
reagent type: catalyst
core: cerium
雜質
≤0.005% heavy metals (as Pb)
≤0.005% insoluble in acid
mp
130 °C (lit.)
負離子痕跡
chloride (Cl-): ≤10 mg/kg
phosphate (PO43-): ≤50 mg/kg
正離子痕跡
Fe: ≤50 mg/kg
SMILES 字串
N.N.N.N.O.O.[Ce+4].OS([O-])(=O)=O.OS([O-])(=O)=O.OS([O-])(=O)=O.OS([O-])(=O)=O
InChI
1S/Ce.4H3N.4H2O4S.2H2O/c;;;;;4*1-5(2,3)4;;/h;4*1H3;4*(H2,1,2,3,4);2*1H2/q+4;;;;;;;;;;/p-4
InChI 密鑰
VCNAMBGKEDPVGQ-UHFFFAOYSA-J
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一般說明
Ammonium cerium(IV) sulfate dihydrate (tetraammonium cerium(IV) sulphate dihydrate) is commonly employed as starting material for various organic syntheses. It is widely employed as oxidizing agent. Its thermal decomposition and thermal characteristics have been reported.
應用
Ammonium cerium(IV) sulfate may be used for the determination of urinary iodine by ammonium persulfate digestion on microplate (APDM) method and colorimetric method.
Ammonium cerium(IV) sulfate was used in thin-layer chromatography for the detection of anti-depreβant drugs in human blood and urine samples.
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。
Clinical chemistry, 43(3), 498-504 (1997-03-01)
We evaluated the clinical utility of an automated HPLC system (Remedi, Bio-Rad) for identification of drugs and metabolites in biological fluids. Serum or urine or both from 354 consecutive cases of poisoning were analyzed by the system and by a
Fast colorimetric method for measuring urinary iodine.
Clinical chemistry, 49(1), 186-188 (2003-01-01)
Clinical chemistry, 46(4), 529-536 (2000-04-12)
Urinary iodine is a good biochemical marker for control of iodine deficiency disorders. Our aim was to develop and validate a simple, rapid, and quantitative method based on the Sandell-Kolthoff reaction, incorporating both the reaction and the digestion process into
Thermal behaviour of sulphato and nitrato complexes of cerium (IV).
J. Therm. Anal., 42(2-3), 343-359 (1994)
Amino acids, 34(2), 315-320 (2006-11-07)
An assessment of the potential of proline to scavenge free radicals was made in a couple of in vitro assay systems, namely graft co-polymerization and autooxidation of pyrogallol. Both these assays are essentially dependent upon free radical mechanisms. Graft co-polymerization
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