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Sigma-Aldrich

Copper(II) perchlorate hexahydrate

98%

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Synonym(s):
Cupric perchlorate hexahydrate
Linear Formula:
Cu(ClO4)2 · 6H2O
CAS Number:
10294-46-9
Molecular Weight:
370.54
EC Number:
237-391-4
MDL number:
MFCD00149666
UNSPSC Code:
12352302
PubChem Substance ID:
24852890
NACRES:
NA.23

Quality Level

100

Assay

98%

form

crystalline

reaction suitability

reagent type: oxidant

density

2.225 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

O.O.O.O.O.O.[Cu++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O

InChI

1S/2ClHO4.Cu.6H2O/c2*2-1(3,4)5;;;;;;;/h2*(H,2,3,4,5);;6*1H2/q;;+2;;;;;;/p-2

InChI key

NHELIHXBJRANPL-UHFFFAOYSA-L

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General description

The monoclinic structure of copper perchlorate hexahydrate was analyzed by X-ray diffraction. The product may be used as a catalyst during the reaction of 5-methylisophthalaldehyde with 1,3-diaminopropane. Benzaldehyde semicarbazones, reacted with copper perchlorate hexahydrate in acetonitrile, may yield corresponding 1,2,4-triazolin-5-ones.

Application

  • Methanol[1-(methoxymethanimidoyl)-2-(pyridin-2-ylmethyl)guanidine]bis(perchlorato)copper(II).: This study reports the synthesis and crystal structure of a new copper(II) complex with potential applications in materials science and catalysis. The research focuses on the structural characterization of the complex, which is crucial for understanding its reactivity and potential uses in various chemical processes (Meenongwa et al., 2012).
  • Oxidative cleavage of DNA by a dipyridoquinoxaline copper(II) complex in the presence of ascorbic acid.: This research explores the catalytic activity of a copper(II) complex in oxidative DNA cleavage. The findings demonstrate the complex′s potential application in biochemical studies and the development of new catalytic processes for DNA manipulation and analysis (Santra et al., 2002).

Pictograms

Flame over circleExclamation mark
GHS03,GHS07

Signal Word

Danger

Hazard Statements

H272,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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)

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Natural flavonoids such as quercetin, (+)catechin and rutin as well as four methoxylated derivatives of quercetin used as models were investigated to elucidate their impact on the oxidant and antioxidant status of human red blood cells (RBCs). The impact of
Sze-Wing Ng et al.
Molecules (Basel, Switzerland), 25(9) (2020-05-01)
A new tetradentate mixed aza-thioether macrocyclic ligand 2,6-dithia[7](2,9)-1,10-phenanthrolinophane ([13]ane(phenN2)S2) was successfully synthesized. Reacting metal precursors [Fe(CH3CN)2(OTf)2], Ni(ClO4)2·6H2O, and Cu(ClO4)2·6H2O with one equivalent of [13]ane(phenN2)S2 afforded [Fe([13]ane(phenN2)S2)(OTf)2] (1), [Ni([13]ane(phenN2)S2)](ClO4)2 (2(ClO4)2), and [Cu([13]ane(phenN2)S2)(OH2)](ClO4)2 (3(ClO4)2), respectively. The structures of [13]ane(phenN2)S2 and all of
The crystal structure of copper perchlorate hexahydrate, Cu (ClO4) 2? 6 H20.
Mani NV and Ramaseshan S
Zeitschrift fur Kristallographie, 115(1-6), 97-109 (1961)
A study of the mechanism of the oxidative cyclization of benzaldehyde semicarbazones induced by cupric perchlorate in acetonitrile
Noto R, et al.
Journal of Heterocyclic Chemistry, 32(4), 1277-1282 (1995)
Complexes of binucleating ligands. III. Novel complexes of a macrocyclic binucleating ligand.
Pilkington NH and Robson R
Australian Journal of Chemistry, 23(11), 2225-2236 (1970)
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