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Key Documents

24-5160

Sigma-Aldrich

Potassium permanganate solution

0.2 M

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About This Item

Empirical Formula (Hill Notation):
KMnO4
CAS Number:
Molecular Weight:
158.03
MDL number:
UNSPSC Code:
12352312
PubChem Substance ID:

form

liquid

reaction suitability

reagent type: oxidant

availability

available only in Japan

concentration

0.2 M
1 N

SMILES string

[K][Mn](=O)(=O)(=O)=O

InChI

1S/K.Mn.4O/q+1;;;;;-1

InChI key

VZJVWSHVAAUDKD-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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(-)
Ming Yang et al.
Nature communications, 6, 6445-6445 (2015-03-12)
Clostrubin is a potent antibiotic against methicillin- and vancomycin-resistant bacteria that was isolated from a strictly anaerobic bacterium Clostridium beijerinckii in 2014. This polyphenol possesses a fully substituted arene moiety on its pentacyclic scaffold, which poses a considerable challenge for
Zhanchao Meng et al.
Nature communications, 6, 6096-6096 (2015-02-05)
Indolosesquiterpenoids are a growing class of natural products that exhibit a wide range of biological activities. Here, we report the total syntheses of xiamycin A and oridamycins A and B, indolosesquiterpenoids isolated from Streptomyces. Two parallel strategies were exploited to

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