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Safety Information

V800294

Sigma-Aldrich

Perchloric acid solution

0.1 N in acetic acid

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About This Item

Linear Formula:
HClO4
CAS Number:
Molecular Weight:
100.46
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:

product line

Vetec

form

liquid

concentration

0.1 N in acetic acid

SMILES string

OCl(=O)(=O)=O

InChI

1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)

InChI key

VLTRZXGMWDSKGL-UHFFFAOYSA-N

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Application

Perchloric acid (in acetic acid) can be used as a detosylating agent for the deprotection of the tosyl functional groups in p-methyl benzene sulfonyl derivatives of primary, secondary aryl amines, and chiral aminoketones. It can also be used in the aromatic mercuration reaction.

Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Flame over circle

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Ox. Liq. 2

Storage Class Code

5.1B - Oxidizing hazardous materials

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Perchloric Acid-Acetic Acid: A Reagent System for Detosylation
Kudav, DP, et al.
Synthetic Communications, 17(10), 1185-1187 (1987)
Perchloric Acid catalyzed aromatic mercuration in acetic acid solution. II. The Substitution Process
Kresge, A and Brennan, J
The Journal of Organic Chemistry, 32(3), 752-755 (1967)
John Greenwood et al.
ACS nano, 9(5), 5520-5535 (2015-04-22)
We shine light on the covalent modification of graphite and graphene substrates using diazonium chemistry under ambient conditions. We report on the nature of the chemical modification of these graphitic substrates, the relation between molecular structure and film morphology, and
Martin G Liebensteiner et al.
Science (New York, N.Y.), 340(6128), 85-87 (2013-04-06)
Perchlorate and chlorate anions [(per)chlorate] exist in the environment from natural and anthropogenic sources, where they can serve as electron acceptors for bacteria. We performed growth experiments combined with genomic and proteomic analyses of the hyperthermophile Archaeoglobus fulgidus that show
Dipanwita Das et al.
Journal of the American Chemical Society, 135(10), 4018-4026 (2013-02-28)
Catalytic four-electron reduction of O2 by ferrocene (Fc) and 1,1'-dimethylferrocene (Me2Fc) occurs efficiently with a dinuclear copper(II) complex [Cu(II)2(XYLO)(OH)](2+) (1), where XYLO is a m-xylene-linked bis[(2-(2-pyridyl)ethyl)amine] dinucleating ligand with copper-bridging phenolate moiety], in the presence of perchloric acid (HClO4) in

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