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3-Sulphophthalic acid, also known as 3-Sulfophthalic acid, is a chemical compound with the molecular formula C8H6O7S. It is a sulfonated derivative of phthalic acid, characterized by a benzene ring with a sulfonic acid group attached at the 3-position. 3-Sulphophthalic acid is soluble in water and exhibits strong acidic properties due to its sulfonic acid group, which makes it suitable for a variety of industrial applications.

67892-43-7

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67892-43-7 Usage

Uses

Used in Dye and Pigment Synthesis:
3-Sulphophthalic acid is used as a key intermediate in the synthesis of dyes and pigments for various applications, including textiles, plastics, and paints. Its strong acidic properties and solubility in water contribute to the stability and color intensity of the resulting dyes and pigments.
Used in Specialty Polymer Production:
In the polymer industry, 3-Sulphophthalic acid serves as a building block for the production of specialty polymers with unique properties, such as high thermal stability, chemical resistance, and enhanced mechanical strength. These polymers find applications in various sectors, including automotive, aerospace, and electronics.
Used as a Corrosion Inhibitor:
3-Sulphophthalic acid is utilized as a corrosion inhibitor in various industrial settings, such as oil and gas pipelines, storage tanks, and cooling systems. Its strong acidic nature helps to prevent metal corrosion by forming a protective layer on the metal surface, thereby extending the service life of the equipment and reducing maintenance costs.
Used in Cleaning and Detergent Formulations:
3-Sulphophthalic acid is incorporated into cleaning and detergent formulations due to its strong acidic properties and water solubility. It enhances the cleaning efficiency of these products by breaking down and removing stubborn stains, grease, and dirt from various surfaces, making it suitable for use in household and industrial cleaning applications.

Check Digit Verification of cas no

The CAS Registry Mumber 67892-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67892-43:
(7*6)+(6*7)+(5*8)+(4*9)+(3*2)+(2*4)+(1*3)=177
177 % 10 = 7
So 67892-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O7S/c9-7(10)4-2-1-3-5(16(13,14)15)6(4)8(11)12/h1-3H,(H,9,10)(H,11,12)(H,13,14,15)

67892-43-7SDS

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 3-sulfophthalic acid

1.2 Other means of identification

Product number -
Other names 3-Sulfo-phthalsaeure

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:67892-43-7 SDS

67892-43-7Synthetic route

phthalic anhydride
85-44-9

phthalic anhydride

A

4-sulfophthalic acid
89-08-7

4-sulfophthalic acid

B

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Conditions
ConditionsYield
With sulfuric acid; sulfur trioxide
phthalic anhydride
85-44-9

phthalic anhydride

sulfuric acid
7664-93-9

sulfuric acid

A

4-sulfophthalic acid
89-08-7

4-sulfophthalic acid

B

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

α-naphthalenesulfamide

α-naphthalenesulfamide

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Conditions
ConditionsYield
With potassium permanganate; water Man dampft die filtrierte Loesung auf ca.1/4 l ein, saeuert mit Salzsaeure an und entfernt die beigemengte Phthalsaeure durch Ausaethern;
3-hydroxy-5-sulfo-[2]naphthoic acid
86-64-6

3-hydroxy-5-sulfo-[2]naphthoic acid

KMnO4

KMnO4

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

phthalic acid sulfinide

phthalic acid sulfinide

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Conditions
ConditionsYield
With hydrogenchloride at 150℃;
indan-4-sulfonic acid
40809-55-0

indan-4-sulfonic acid

potassium permanganate

potassium permanganate

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

hydrogenchloride
7647-01-0

hydrogenchloride

1,1,3-trioxo-2,3-dihydro-1λ6-benz[d]isothiazole-4-carboxylic acid ; N potassium salt

1,1,3-trioxo-2,3-dihydro-1λ6-benz[d]isothiazole-4-carboxylic acid ; N potassium salt

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Conditions
ConditionsYield
at 150℃;
2C8H6O7S*3C10H8N2*C10H8*2H2O4S

2C8H6O7S*3C10H8N2*C10H8*2H2O4S

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Conditions
ConditionsYield
Stage #1: 2C8H6O7S*3C10H8N2*C10H8*2H2O4S With sodium hydroxide In water
Stage #2: With hydrogenchloride In water pH=2;
azorubine
3567-69-9

azorubine

A

3-hydroxyphthalic acid
601-97-8

3-hydroxyphthalic acid

B

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

C

benzene-1,2-dicarboxylic acid
88-99-3

benzene-1,2-dicarboxylic acid

Conditions
ConditionsYield
Stage #1: azorubine With titanium(IV) oxide In water at 50℃; for 2h;
Stage #2: With dihydrogen peroxide In water Catalytic behavior;
1,10-Phenanthroline
66-71-7

1,10-Phenanthroline

zinc uranyl acetate heptahydrate

zinc uranyl acetate heptahydrate

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

Zn(1,10-phenanthroline)3(UO2)2(3-sulfoisophthalate)2

Zn(1,10-phenanthroline)3(UO2)2(3-sulfoisophthalate)2

Conditions
ConditionsYield
In water at 160℃; for 48h; pH=1.5; Autoclave; High pressure;39%
3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

3-sulfophthalimide
115953-80-5

3-sulfophthalimide

Conditions
ConditionsYield
Stage #1: 3-sulfophthalic acid at 150℃; for 3h;
Stage #2: With urea at 130℃;
2.5%
4-sulfophthalic acid
89-08-7

4-sulfophthalic acid

3-sulfophthalic acid
67892-43-7

3-sulfophthalic acid

3-Carboxyphenol
99-06-9

3-Carboxyphenol

Conditions
ConditionsYield
With sodium hydroxide In water; nickel

67892-43-7Downstream Products

67892-43-7Relevant academic research and scientific papers

Separation of isomers of sulfophthalic acid by guest induced host framework formation with 4,4′-bipyridine

Mahata, Goutam,Roy, Sandipan,Biradha, Kumar

, p. 6614 - 6616 (2011)

The selective inclusion of aromatic guest molecules in host frameworks formed by 3-sulfophthalic acid or 4-sulfophthalic acid and 4,4′-bipyridine has been effectively utilized for the separation of sulfophthalic acid isomers.

Ti(iv) oxalate complex-derived hierarchical hollow TiO2 materials with dye degradation properties in water

Zhang, Ye,Qiao, Zhen-An,Liu, Junmin,Wang, Xue,Yao, Shuo,Wang, Tao,Liu, Bing,Ma, Yali,Liu, Yunling,Huo, Qisheng

, p. 265 - 270 (2015/12/24)

Ti(iv)-based complexes have been demonstrated as candidates for preparing hybrid and functional materials, and have received considerable attention. In this paper, hierarchical hollow titania materials with different surface nanostructures were synthesized successfully using a hydrothermal process via the transformation of a Ti(iv) oxalate complex as a precursor. Different concentrations of ammonia were used to adjust the morphologies and crystalline forms of the hydrothermal products. The hierarchical hollow anatase titania materials, HHTM-1 (cal) and HHTM-2 (cal), have high surface areas of up to 132 m2 g-1 and 84 m2 g-1, respectively, and show superior performance for dye degradation in water.

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