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7781-49-9

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7781-49-9 Usage

Purification Methods

Dissolve it in boiling dioxane (20g in 300mL), add H2O (100mL) slowly, cool, filter and dry it in vacuo at 100o. Its solubility in CHCl3 is ~1%. [UV: Fox & Atkinson J Am Chem Soc 72 3629 1950, Beilstein 26 III/IV 1776.]

Check Digit Verification of cas no

The CAS Registry Mumber 7781-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7781-49:
(6*7)+(5*7)+(4*8)+(3*1)+(2*4)+(1*9)=129
129 % 10 = 9
So 7781-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H14IN5O2/c20-15-6-8-16(9-7-15)21-23-19(14-4-2-1-3-5-14)24-22-17-10-12-18(13-11-17)25(26)27/h1-13,22H/b23-21+,24-19+

7781-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-iodophenyl)imino-N'-(4-nitroanilino)benzenecarboximidamide

1.2 Other means of identification

Product number -
Other names p-IODONITROTETRAZOLIUMFORMAZAN

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:7781-49-9 SDS

7781-49-9Downstream Products

7781-49-9Relevant academic research and scientific papers

Synthesis, crystal structure and antiradical effect of copper(ii) Schiff base complexes containing five-, six- and unusual seven-membered rings

Puterova, Zita,Valentova, Jindra,Bojkova, Zuzana,Koiek, Jozef,Devinsky, Ferdinand

, p. 1484 - 1490 (2011)

The synthesis and solid-state structure of mononuclear copper(ii) complexes [Cu(SAIB)(H2O)2] (1), [Cu(SBAIB)(H2O) 2]·H2O (2) and [Cu(SGABA)(H2O) 2] (3) are described. Schiff base

In vitro studies regarding the antioxidant effects of procaine, gerovital H3 and aslavital

Gradinaru, Daniela,Margina, Denisa,Borsa, Claudia

experimental part, p. 761 - 766 (2010/09/03)

Gerovital H3 (GH3) and Aslavital are Romanian procaine based drugs used in the prophylaxis of aging for over 40 years. By the use of in vitro experimental models, the main purpose of the present study was to evaluate the antioxidant effects of these anti-aging products with regard to the superoxide radical generation in an enzymatic system, xanthine - xanthine oxidase - INT [2-(4-iodophenyl)-3-(4-nitrophenol)-5-phenyltetrazolium chloride], as well as with regard to the susceptibility of human low density lipoprotein to oxidation (oxLDL), corresponding to conjugated dienes formation. At 10 mM in reference to procaine concentration, the maximum of inhibition was exerted by Aslavital (88%) followed by GH3 (62%), whereas procaine hydrochloride had a slight inhibitory effect upon the INT reduction. We pointed out a significant inhibition of Cu2+- induced oxLDL after 20 and 60 minutes in the presence of Aslavital at all the concentrations tested (0.1; 0.5 and 1 mM, related to procaine final concentration in the reaction system), while GH3 exerted a significant decrease in oxLDL only at the highest concentration (1mM procaine).

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