60467
高锰酸钾
tested according to Ph. Eur.
别名:
高锰酸钾
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关于此项目
经验公式（希尔记法）:
KMnO4
化学文摘社编号:
分子量:
158.03
UNSPSC Code:
12352300
PubChem Substance ID:
EC Number:
231-760-3
MDL number:
InChI key
VZJVWSHVAAUDKD-UHFFFAOYSA-N
InChI
1S/K.Mn.4O/q+1;;;;;-1
SMILES string
[K+].[O-][Mn](=O)(=O)=O
agency
USP/NF, tested according to Ph. Eur.
assay
99.0-100.5%
form
crystalline
reaction suitability
reagent type: oxidant
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Application
适用于非均相氧化。
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Ox. Sol. 2 - Repr. 2 - Skin Corr. 1 - STOT RE 2 Inhalation
target_organs
Brain
存储类别
5.1B - Oxidizing hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
易制毒化学品（3类）
易制爆化学品
危险化学品
此项目有
Jessica M Terry et al.
Talanta, 99, 1051-1056 (2012-09-13)
We have explored the chemiluminescence response of amino acids and related compounds (including the tripeptide glutathione, and disulfides: cystine, homocystine and glutathione disulfide) with several new adaptations of the permanganate and tris(2,2'-bipyridine)ruthenium(III) ([Ru(bipy)(3)](3+)) reagents and a recently developed colloidal manganese(IV)
Matthias V Westphal et al.
ChemMedChem, 10(3), 461-469 (2015-01-30)
The tert-butyl group is a common motif in medicinal chemistry. Its incorporation into bioactive compounds is often accompanied by unwanted property modulation, such as increased lipophilicity and decreased metabolic stability. Several alternative substituents are available for the drug discovery process.
Darryl B Jones et al.
Water research, 46(17), 5491-5498 (2012-08-15)
In this study, the impacts of three preoxidation strategies [i.e., using potassium permanganate (KMnO(4)), chlorine dioxide (ClO(2)), or hydrogen peroxide (H(2)O(2))] before preformed monochloramine (NH(2)Cl) addition on the formation and speciation of iodinated trihalomethanes (I-THMs) were evaluated at the Br(-)/I(-)
Arnaud Beduneau et al.
PloS one, 4(2), e4343-e4343 (2009-02-03)
We posit that the same mononuclear phagocytes (MP) that serve as target cells and vehicles for a host of microbial infections can be used to improve diagnostics and drug delivery. We also theorize that physical and biological processes such as
F C Holstege et al.
Methods (San Diego, Calif.), 12(3), 203-211 (1997-07-01)
Open complex formation precedes initiation of transcription by RNA polymerases. In the analysis of transcription initiation from eukaryotic class II promoters, we have used promoter DNA structures that represent intermediates in open complex formation. We describe the preparation and isolation
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