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3-Methoxysulphanilic acid, also known as 3-Methoxybenzenesulfonic acid, is a chemical compound with the molecular formula C7H9NO4S. It is a white to light yellow crystalline powder that is commonly used in the production of dyes and pigments, as well as in the synthesis of pharmaceuticals and other organic compounds. This versatile chemical also serves as a reagent in chemical reactions and a corrosion inhibitor. However, it is important to handle 3-methoxysulphanilic acid with care, as it is harmful if swallowed, inhaled, or absorbed through the skin, and may cause irritation to the respiratory system and skin.

6472-58-8

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6472-58-8 Usage

Uses

Used in Dye and Pigment Production:
3-Methoxysulphanilic acid is used as a key intermediate in the production of dyes and pigments, contributing to the coloration and stability of these substances in various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 3-Methoxysulphanilic acid is utilized as a building block for the synthesis of various drugs, playing a crucial role in the development of new medications.
Used as a Reagent in Chemical Reactions:
3-Methoxysulphanilic acid serves as a reagent in a wide range of chemical reactions, facilitating the synthesis of different organic compounds and contributing to the advancement of chemical research and development.
Used as a Corrosion Inhibitor:
3-Methoxysulphanilic acid is employed as a corrosion inhibitor, protecting materials from the damaging effects of corrosion and extending their service life in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6472-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6472-58:
(6*6)+(5*4)+(4*7)+(3*2)+(2*5)+(1*8)=108
108 % 10 = 8
So 6472-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO4S/c1-12-7-4-5(13(9,10)11)2-3-6(7)8/h2-4H,8H2,1H3,(H,9,10,11)

6472-58-8SDS

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 4-amino-3-methoxybenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 3-Methoxysulfanilic 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:6472-58-8 SDS

6472-58-8Upstream product

6472-58-8Downstream Products

6472-58-8Relevant academic research and scientific papers

Solid state synthesis of ring-substituted aminobenzenesulphonic acids

Kapoor, Inder Pal Singh,Kapoor, Manisha,Singh, Gurdip

experimental part, p. 1556 - 1560 (2011/02/23)

Treatment of 2-methoxyaniline and 3,5-dichloroaniline with conc.H 2SO4 in 2:1 molar ratio at RT affords the corresponding sulphate salts. These salts have been characterized by X-ray diffraction and spectral analyses. Both these salts are found to form ring substituted aminobenzenesulphonic acids in solid state, via proton transfer, under thermal and microwave irradiations.

A study on the sulfonation of aromatic amines with sulfuric acid under microwave irradiation

Li, Hui-Zhang,Xiao, Li-Wei,Li, Hong-Ya,Wang, Kai-Fang,Li, Xu

, p. 493 - 494 (2007/10/03)

The sulfonation of aromatic amines with high yields, simple operations and short reaction time has been studied under microwave irradiation in solvent-free conditions.

Sulfonation of arylamines Part 9 - Solid state synthesis of di-ortho ring substituted aminobenzenesulfonic acids

Singh, Gurdip,Kapoor, Inder Pal Singh,Singh, Jyotsna

, p. 1114 - 1117 (2007/10/03)

Di-ortho ring substituted arylammonium sulfates (Di-o-RSAS) have been prepared from the corresponding arylamines by treatment with conc. H2SO4 and characterized by elemental, gravimetric and spectral analyses. These sulfates yield the corresponding ring substituted aminobenzenesulfonic acids (RSABSA) when subjected to thermal energy. Non-isothermal gravimetric studies on di-o-RSAS support the formation of RSABSA. It is observed that most of the salts undergo transformation to acid in solid state via proton transfer reaction prior to sulfonation.

Alkanol substituted disazo orange dye for nylon

-

, (2008/06/13)

The specification describes a new group of alkanol substituted disazo compounds that are useful in dyeing polyamide textile fibers in orange hues. The new compounds are compatible with several acid blue dyes and several acid red dyes that are commercially important as dyes for nylon. The new compounds are particularly well suited for use as the "yellow" component in trichromatic systems for dying polyamide carpeting and other textiles. The new compounds are relatively inexpensive to make and have outstanding application and fastness properties. Other aspects of the specification are concerned with a method of making the new compounds and with a method of dyeing polyamides with said compounds and to the novel dyed polyamides resulting from the use of the new group of compounds as dyes.

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