6361-37-1 Usage
Description
1-naphthol-4,7-disulfonic acid is a compound that consists of naphthol and sulfonic acid groups, known for its ability to change color in response to changes in acidity.
Uses
Used in Dye Synthesis:
1-naphthol-4,7-disulfonic acid is used as a precursor in the production of azo dyes for its solubility in water and its role in dyeing processes.
Used in Textile Industry:
1-naphthol-4,7-disulfonic acid is used as a dye ingredient for coloring textiles, due to the azo dyes' variety of colors and their application in this industry.
Used in Plastics Industry:
1-naphthol-4,7-disulfonic acid is used as a coloring agent in the plastics industry, where azo dyes provide a range of color options for plastic products.
Used in Printing Industry:
1-naphthol-4,7-disulfonic acid is used as a component in ink formulations for the printing industry, taking advantage of the colorfast properties of azo dyes.
Used as a pH Indicator:
1-naphthol-4,7-disulfonic acid is used as a pH indicator due to its color-changing properties in response to acidity levels.
Used in Chemical Research and Analysis:
1-naphthol-4,7-disulfonic acid is used as a reagent or standard for calibration in chemical research and analysis, benefiting from its solubility and color-changing characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 6361-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6361-37:
(6*6)+(5*3)+(4*6)+(3*1)+(2*3)+(1*7)=91
91 % 10 = 1
So 6361-37-1 is a valid CAS Registry Number.
6361-37-1Relevant articles and documents
Sulfonation of 1- and 2-naphthol and their methanesulfonate esters with sulfur trioxide. The influence of initial sulfation on the sulfo-product composition
Ansink, Harold R. W.,Zelvelder, Erwin,Cerfontain, Hans
, p. 210 - 215 (2007/10/02)
The sulfonation of 1- and 2-naphthol with sulfur trioxide in C(2)H3NO2 has been studied by using 1H NMR. 1-Naphthol (1) yields, upon reaction with 1.0 mol-equiv of SO3, a mixture of 2- and 4-sulfonic acids (2- and 4-S); upon increasing the reaction temperature, the relative amount of 2-S increases.Upon reaction with 4.0 mol-equiv of SO3, the initially observed products are the hydrogen sulfate 1-O,2,4-S3 and some corresponding sulfonic anhydrides.After prolonged reaction times, some 1-O-4,7-S3 is formed. 2-Naphthol (3), upon reaction with 1.0 mol-equiv of SO3, yields a 85:15 mixture of 1-S and 8-S, whereas upon reaction with 2.0 mol-equiv of SO3, a 8:14:78 mixture of 5-S, 6-S and 8-S are formed.Sulfonation of 3, either by (i) reaction with 1.2 and, subsequently, an additional 2.0 mol-equiv of SO3, or (ii) by direct addition of 4.0 mol-equiv of SO3, yields a mixture of the carbyl sulfates 5-5-S and 5-6-S and the hydrogen sulfate 3-O,6,8-S3, the relative yield depending on the method used.The results are discussed in terms of initial formation of the corresponding naphthyl hydrogen sulfates and on the basis of a comparison with the reactions of 1- and 2-naphthyl methanesulfonates, the chosen model compounds for the hydrogen sulfates, with SO3.