215392
Copper(II) perchlorate hexahydrate
98%
Synonym(s):
Cupric perchlorate hexahydrate
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About This Item
Linear Formula:
Cu(ClO4)2 · 6H2O
CAS Number:
Molecular Weight:
370.54
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
Assay:
98%
Form:
crystalline
Quality Level
Assay
98%
form
crystalline
reaction suitability
core: copper
reagent type: oxidant
density
2.225 g/mL at 25 °C (lit.)
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).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
5.1A - Strongly oxidizing hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Sabri Ahmed Cherrak et al.
PloS one, 11(10), e0165575-e0165575 (2016-10-28)
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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