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Benzoic acid, 4-methyl-, copper(1+) salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79580-25-9

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79580-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79580-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,8 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79580-25:
(7*7)+(6*9)+(5*5)+(4*8)+(3*0)+(2*2)+(1*5)=169
169 % 10 = 9
So 79580-25-9 is a valid CAS Registry Number.

79580-25-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name copper(II) para-methylbenzoate

1.2 Other means of identification

Product number -
Other names copper(II) para-toluate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79580-25-9 SDS

79580-25-9Relevant academic research and scientific papers

Synthesis, magnetic and spectroscopic characterization of copper(II) toluate complexes with substituted piperazines

Manhas,Sardana,Kalia

, p. 171 - 179 (2005)

New copper(II) toluate complexes with the saturated heterocyclic bases [(L-L) having the tendency to coordinate through both 1 and 4 nitrogen atoms] 1-methylpiperazine, 1,4-dimethylpiperazine, 2,6-dimethylpiperazine and 1-phenylpiperazine have been prepared and characterized by physico-chemical and spectroscopic methods. All of the complexes were found to be antiferromagnetic with stoichiometries of the type Cu(OOCR)2(L-L)n (n = 1 or 0.5, R = 2-, 3-or 4-CH3C6H4) except Cu(OOCC6H4CH3-4)2(L-L) (where L-L = 2,6-dimethylpiperazine), which is magnetically dilute. The spin exchange parameter, -2J, for two of the antiferromagnetic complexes has been evaluated from magnetic susceptibility measurements at different temperatures. Binuclear copper(II) acetate monohydrate-like structure for the antiferromagnetic complexes of 1:1 stoichiometry and polymeric structure of the type Cu(OOCH) 2(dioxan)0.5 for the complexes of 1:0.5 stoichiometry have been proposed. The magnetically dilute complex has been assigned a polynuclear trans-pseudo-octahedral or polymeric square pyramidal structure. Copyright

Synthesis, crystal structure, and DNA-binding properties of a new copper (II) complex containing mixed-ligands of 2,2′-bipyridine and p-methylbenzoate

Liu, Fa Qian,Wang, Qing Xiang,Jiao, Kui,Jian, Fang Fang,Liu, Guang Ye,Li, Rong Xun

, p. 1524 - 1530 (2008/10/09)

A novel copper complex of [Cu(bpy)(pba)2·H 2O]·0.5H2O (bpy = 2,2′-bipyridine, pba = p-methylbenzoate) was synthesized. The interaction of the complex to native fish sperm DNA was investigated through electrochemistry, electronic absorption spectroscopy and viscosity experiments. In the X-ray crystallography structure, the copper (II) ion is coordinated by two oxygen atoms of two p-methylbenzoate groups, two nitrogen atoms of 2,2′-bipyridine and one water molecule. The observed changes in the physicochemical features of the copper (II) complex on binding to DNA suggested that the complex bind to DNA with intercalation mode via 2,2′-bipyridine ring into DNA base pairs. Electrochemical studies revealed that the complex prefer to bind to DNA in Cu(I) form rather than Cu(II) oxidation state form. Additionally, the nuclease activity of the title complex was assessed by gel electrophoresis assay and the results shown that the copper complex can cleave pBR322 DNA effectively in the presence of ascorbic acid.

Effects of Methyl Substituent on Solvent Extraction of Copper(II) with o-, m-, and p-Methylbenzoic Acids.

Yamada, Hiromichi,Horikawa, Shiho,Fujii, Yukio,Mizuta, Masateru

, p. 835 - 840 (2007/10/02)

The extraction of copper(II) with o-, m-, and p-methylbenzoic acids in 1-octanol was carried out at 25 deg C and aqueous ionic strength of 0.1 mol dm-3 (NaClO4).In contrast to the extraction with benzoic acid, in which only the monomeric copper(II) benzoate is extracted, the dimeric copper(II) species is also responsible for the extraction of copper(II) with o- and m-methylbenzoic acids in 1-octanol together with the monomeric one.On the other hand, p-methylbenzoic acid has a poorer extracting capability than o- and m-methylbenzoic acids and only the monomeric copper(II) species is responsible for the extraction.

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