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Dimethylsulfonazo III (DMSA) is a chemical compound widely used as a colorimetric reagent for the determination of trace metal ions, particularly copper, in various samples such as water, soil, and biological tissues. It forms a stable, water-soluble complex with copper ions, which can be easily detected and quantified using spectrophotometry. DMSA is also known for its chelating properties, which enable it to bind to metal ions and facilitate their removal from the body, making it a potential therapeutic agent for heavy metal poisoning. However, it is important to note that DMSA is not approved for clinical use in humans, and its safety and efficacy as a chelator are still subjects of ongoing research.

1479-11-4

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1479-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1479-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1479-11:
(6*1)+(5*4)+(4*7)+(3*9)+(2*1)+(1*1)=84
84 % 10 = 4
So 1479-11-4 is a valid CAS Registry Number.

1479-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name DIMETHYLSULFONAZO III

1.2 Other means of identification

Product number -
Other names 2,7-BIS[(4-METHYL-2-SULFOPHENYL)AZO]-1,8-DIHYDROXYNAPHTHALENE-3,6-DISULFONIC ACID

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:1479-11-4 SDS

1479-11-4Relevant academic research and scientific papers

Action of metal and organometallic halides and pseudohalides towards stannoxanes

Singhal, Kiran,Chaudhary, Subhas Kumar,Prakash, Om

, p. 9020 - 9022 (2013/11/19)

Interactions of HgX2 (X = Cl, Br, I, SCN, CN, NCO), SbCl3, TeCl4 and PhTeCl3 with (p-FC6H 4)3Sn-O-Sn(p-FC6H4)3 at room temperature have been found to procee

THE PREPARATION OF PHENYL SUBSTITUTED ANTIMONY(III) AND ANTIMONY(V) CHLORIDES AND BROMIDES

Nunn, Michael,Sowerby, D. Bryan,Wesolek, Denise M.

, p. C45 - C46 (2007/10/02)

In the absence of solvent, the redistribution of 2/1 and 1/2 molar mixtures of Ph3Sb and SbX3, where X = Cl or Br, is rapid giving quantitative yields of Ph2SbX and PhSbX2, respectively.

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