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Merck

24-1060

Perchloric acid

0.1 M

Synonym(s):

PCA

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About This Item

Linear Formula:
HClO4
CAS Number:
7601-90-3
Molecular Weight:
100.46
UNSPSC Code:
12352106
PubChem Substance ID:
329752568
MDL number:
MFCD00011325
Concentration:
0.1 M
1/10 N
Form:
liquid

Key Documents

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Product Name

Perchloric acid, 0.1 M

InChI

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

SMILES string

OCl(=O)(=O)=O

InChI key

VLTRZXGMWDSKGL-UHFFFAOYSA-N

form

liquid

reaction suitability

reagent type: oxidant

availability

available only in Japan

concentration

0.1 M
1/10 N

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Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

5.1B - Oxidizing hazardous materials

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

24-1060-5-500ML-J:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
U1337
U7265
U1077
U2976
U2933

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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
Dipanwita Das et al.
Journal of the American Chemical Society, 135(7), 2825-2834 (2013-02-12)
Selective two-electron plus two-proton (2e(-)/2H(+)) reduction of O(2) to hydrogen peroxide by ferrocene (Fc) or 1,1'-dimethylferrocene (Me(2)Fc) in the presence of perchloric acid is catalyzed efficiently by a mononuclear copper(II) complex, [Cu(II)(tepa)](2+) (1; tepa = tris[2-(2-pyridyl)ethyl]amine) in acetone. The E(1/2)
Kristiina Cajanus et al.
The journal of pain : official journal of the American Pain Society, 15(12), 1248-1256 (2014-09-23)
Most clinically used opioids are mu-opioid receptor agonists. Therefore, genetic variation of the OPRM1 gene that encodes the mu-opioid receptor is of great interest for understanding pain management. A polymorphism 118A>G (rs1799971) within the OPRM1 gene results in a missense
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