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Merck
CN

10334

Sigma-Aldrich

次硝酸铋(III)

puriss., meets analytical specification of USP, 71-74% Bi basis (calc. on dried substance)

别名:

硝酸氧化铋, 硝酸氧铋(III), 碱式硝酸铋(III)

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关于此项目

线性分子式:
Bi5O(OH)9(NO3)4
化学文摘社编号:
分子量:
1461.99
EC 号:
MDL编号:
UNSPSC代码:
12352302
PubChem化学物质编号:
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等级

puriss.

方案

71-74% Bi basis (calc. on dried substance)

质量

meets analytical specification of USP

杂质

residual solvents, complies
≤0.01% ammonium (NH4)
≤0.5% sub.not precip.b.NH4OH(SO4)

缺失

≤3% loss on drying, 105 °C

痕量阴离子

chloride (Cl-): ≤200 mg/kg
sulfate (SO42-): ≤300 mg/kg

痕量阳离子

Ag: ≤0.0025%
As: ≤2 mg/kg
Cu: ≤50 mg/kg
Pb: ≤20 mg/kg

SMILES字符串

O[Bi]=O.O[Bi](O)O[N+]([O-])=O.O[Bi](O)O[N+]([O-])=O.O[Bi](O)O[N+]([O-])=O.O[Bi](O)O[N+]([O-])=O

InChI

1S/5Bi.4NO3.9H2O.O/c;;;;;4*2-1(3)4;;;;;;;;;;/h;;;;;;;;;9*1H2;/q+1;4*+3;4*-1;;;;;;;;;;/p-9

InChI key

OAVDTZZNYFIIGB-UHFFFAOYSA-E

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储存分类代码

13 - Non Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Wesolowski
Arzneimittel-Forschung, 28(3), 372-378 (1978-01-01)
A survey is given of the pharmacopoeial preparations of inorganic Bi(III) compounds: bismuth subnitrate and bismuth subcarbonate. The use of these preparations, methods of preparation, qualitative and quantitative assays have been reviewed.
I Mori et al.
Talanta, 35(11), 879-883 (1988-11-01)
A simple and sensitive spectrophotometric determination of bismuth(III) is based on the reaction between bismuth(III) and o-hydroxyhydroquinonephthalein in the presence of Brij 58 in acidic media. The calibration graph is linear over the range 0-3.5 mug/ml bismuth(III) in the final
Selective nitration of aromatic compounds with bismuth subnitrate and thionyl chloride.
Muathen HA.
Molecules (Basel), 8(7), 593-598 (2003)
[PPI plus bismuth-based quintuple therapy].
Ken Kimura et al.
Nihon rinsho. Japanese journal of clinical medicine, 63 Suppl 11, 452-458 (2005-12-21)
Yukihiro Kondo et al.
Cancer chemotherapy and pharmacology, 53(1), 33-38 (2003-10-08)
Attenuation of the renal toxicity of cis-diamminedichloroplatinum (CDDP) is important in the use of this effective but cytotoxic anticancer agent. We have previously shown that the renal toxicity of CDDP can be efficiently reduced by the induction of metallothionein (MT)

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