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118876-56-5

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118876-56-5 Usage

Physical form

white to light yellow crystalline powder

Use

reagent for the determination of trace amounts of silver, intermediate in the production of various pharmaceutical and agricultural chemicals

Potential applications

photography as a photosensitizer, synthesis of dyes and pigments

Chemical category

aromatic amine, sulfonamide

Handling precautions

potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 118876-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,7 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 118876-56:
(8*1)+(7*1)+(6*8)+(5*8)+(4*7)+(3*6)+(2*5)+(1*6)=165
165 % 10 = 5
So 118876-56-5 is a valid CAS Registry Number.

118876-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-diaminonaphthalene-1-sulfonamide

1.2 Other means of identification

Product number -
Other names 1-Naphthalenesulfonamide,5,6-diamino

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:118876-56-5 SDS

118876-56-5Downstream Products

118876-56-5Relevant articles and documents

THE POLAROGRAPHIC AND VOLTAMMETRIC DETERMINATION OF 2-AMINO-5-SULPHOAMOYLNAPHTHALENE-AZO-(2'-CHLORO-4'-NITROBENZENE)

Barek, Jiri,Balsiene, Jana,Berka, Antonin,Hauserova, Ivana,Zima, Jiri

, p. 19 - 33 (2007/10/02)

The polarographic reduction of the title azo dye was studied, a mechanism was suggested and optomal conditions were determined for analytical utilization of this process.A detection limit of 3*10-7 mol l-1 was obtained using fast scan differential pulse voltammetry and 0.7*10-7 mol l-1 using linear potential scan voltammetry at a hanging mercury drop electrode.The detection limit can be decreased by adsorptive accumulation of the determined substance on the surface of hanging mercury drop electrode, to 1*10-8 mol l-1 for fast scan differential pulse voltammetry and 0.6*10-8 mol l-1 for linear scan voltammetry.The selectivity of the determination can be improved by preliminary separation by extraction or thin-layer chromatography.

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