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14494-37-2

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14494-37-2 Usage

Uses

Copper(II)-protoporphyrin IX is a biocompatible polymeric micro and nanocapsules and is used as antimalaric.

Check Digit Verification of cas no

The CAS Registry Mumber 14494-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,9 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14494-37:
(7*1)+(6*4)+(5*4)+(4*9)+(3*4)+(2*3)+(1*7)=112
112 % 10 = 2
So 14494-37-2 is a valid CAS Registry Number.

14494-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(1Z,4Z,10Z,14Z)-18-(2-carboxyethyl)-7,12-bis(ethenyl)-3,8,13,17-tetramethylporphyrin-21,22,23,24-tetraid-2-yl]propanoic acid,copper

1.2 Other means of identification

Product number -
Other names copper protoporphyrin IX

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:14494-37-2 SDS

14494-37-2Downstream Products

14494-37-2Relevant articles and documents

Reactions of Copper(I) with Micellar Porphyrins and Hemes. Spectroscopic Evidence for Copper(I)-Heme Binuclear Ion Formation

Deardorff, Eugene A.,Carr, Paulette A. G.,Hurst, James K.

, p. 6611 - 6616 (1981)

Addition of cuprous ion to sodium dodecyl sulfate solubilized porphyrins and ferrihemes containing olefinic substituent groups gives rise to spectral perturbations diagnostic of Cu(I) ? complexation.The hemes undergo slow subsequent demetalation in acidic solution, forming porphyrin dications; in the presence of high concentrations of Cu(II) ion the corresponding cupriporphyrins are also formed.For ferriprotoporphyrin IX, the rate of product formation is inversely dependent upon the Cu(II) ion concentration; the data are interpreted in terms of a reaction mechanism, the central feature of which is a dynamic equilibrium between oxidized and reduced hemes, i.e., FeIIIPPIX-CuI + Cu(I) = FeIIPPIX-CuI + Cu(II).This interpretation is supported by the observation that the hemes containing electron-withdrawing substituents in β-pyrrolic positions are extensively reduced to the ferro state by copper(I), but hemes lacking these groups remain primarily ferric when mixed with the cuprous reagent.The reduced Fe(II)-Cu(I) and mixed-valent Fe(III)-Cu(I) binuclear ions are discussed as potential structural models for the oxygen-binding site in cytochrome oxidase.

Impact of metal ions in porphyrin-based applied materials for visible-light photocatalysis: Key information from ultrafast electronic spectroscopy

Kar, Prasenjit,Sardar, Samim,Alarousu, Erkki,Sun, Jingya,Seddigi, Zaki S.,Ahmed, Saleh A.,Danish, Ekram Y.,Mohammed, Omar F.,Pal, Samir Kumar

, p. 10475 - 10483 (2014/08/18)

ProtoporphyrinIX-zinc oxide (PP-ZnO) nanohybrids have been synthesized for applications in photocatalytic devices. High-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and steady-state infrared, absorption, and emission spect

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