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alpha,beta,gamma,delta-tetrakis(4-N-trimethylaminophenyl)porphine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69458-19-1

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69458-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69458-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,5 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69458-19:
(7*6)+(6*9)+(5*4)+(4*5)+(3*8)+(2*1)+(1*9)=171
171 % 10 = 1
So 69458-19-1 is a valid CAS Registry Number.

69458-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[4-[10,15,20-tris[4-(trimethylazaniumyl)phenyl]-21,22-dihydroporphyrin-5-yl]phenyl]azanium

1.2 Other means of identification

Product number -
Other names TTAP

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:69458-19-1 SDS

69458-19-1Relevant articles and documents

Ionic interactions of anionic thiacalix[4]arene with cationic porphyrins

Garg, Bhaskar,Bisht, Tanuja,Chauhan, Shive Murat Singh

experimental part, p. 161 - 178 (2010/09/11)

A facile synthesis of 25,26,27,28-tetrakis(alkyloxy)-2,8,14,20- tetrathiacalix[4]arene-5,11,17,23-tetrasulfonate via ipso substitution of p-tert-butylthiacalix[4]arene tetraalkyl ether with sulfuric acid is described. Ionic interaction of anionic thiacalix[4]arene and cationic porphyrins were quantitatively studied by UV-vis, fluorescence, 1H NMR and ESI-MS spectrometry. Binding constants were in the range of 10 8 M -1. Binding with axial ligands was investigated and formation of ternary complexes was recognized with pyridine, 4-methylpyridine and Nmethylimidazole. The factors affecting the interaction process including pH, solvents and salts were also examined in detail. The results indicated that the neutral medium (pH = 7) is most favorable for electrostatic interactions. ARKAT USA, Inc.

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