88-90-4 Usage
Description
2,6-Dinitrotoluene-4-sulfonic acid, with the molecular formula C7H6N2O7S, is a chemical compound derived from toluene. It features two nitro groups and a sulfonic acid group, giving it unique properties and applications in various industries.
Uses
Used in Chemical Synthesis:
2,6-Dinitrotoluene-4-sulfonic acid is used as an intermediate in the synthesis of other chemicals, playing a crucial role in the production of various compounds.
Used in Dye and Pigment Production:
2,6-DINITROTOLUENE-4-SULFONIC ACID is utilized as a key component in the creation of dyes and pigments, contributing to the coloration and stability of these products.
Used in Pesticide and Herbicide Degradation:
2,6-Dinitrotoluene-4-sulfonic acid is a potential degradation product of certain pesticides and herbicides, indicating its involvement in the breakdown and environmental impact of these agricultural chemicals.
It is important to handle 2,6-dinitrotoluene-4-sulfonic acid with care, as it is a yellow to orange solid that is soluble in water and other polar solvents. Due to its potential harmful effects if ingested or inhaled, and its ability to cause skin and eye irritation, proper safety measures should be taken during its use and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 88-90-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88-90:
(4*8)+(3*8)+(2*9)+(1*0)=74
74 % 10 = 4
So 88-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O7S/c1-4-2-5(8(10)11)7(17(14,15)16)6(3-4)9(12)13/h2-3H,1H3,(H,14,15,16)
88-90-4Relevant articles and documents
Synthesis of reference substances for highly polar metabolites of nitroaromatic compounds
Schmidt, Torsten C.,Steinbach, Klaus,Buetehorn, Ulf,Heck, Kerstin,Volkwein, Ute,Stork, Gottfried
, p. 3119 - 3130 (2007/10/03)
Transformation processes of nitroaromatic compounds (NAC) lead to polar and highly hydrophilic metabolites. For the unequivocal identification of proposed metabolites reference substances are needed. Since most of them are not commercially available, their synthesis was done in our group. In many cases no satisfying synthesis schemes were found in the literature. In this communication, we therefore describe the preparation, structural elucidation and separation of 17 compounds. Many of the newly synthesized analytes were found in various water samples from a former ammunition plant.
