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DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT(DPAS), also known as DBS acid barium salt, is an organic compound with a chemical formula of C12H11NO3S·Ba. It is a white powder. Solubility is very low. Its solubility in water is 2 mg/L, while the solubility in methanol and ethanol is 1.3 and 0.32 g/L, respectively. A relatively stable compound. At room temperature, it can be stored for years without decomposing. However, in a humid environment, DBS acid barium salt may be affected by moisture and decompose. It is an important organic molecular compound, which is widely used in biomedicine, chemistry, materials and other fields.

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Chemical Formula |
C24H20BaN2O6S2 |
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Exact Mass |
634 |
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Molecular Weight |
634 |
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m/z |
634 (100.0%), 635 (16.2%), 633 (15.7%), 632 (11.0%), 635 (9.7%), 631 (9.2%), 636 (9.0%), 630 (3.4%), 636 (3.2%), 633 (2.8%), 634 (2.5%), 637 (2.3%), 635 (1.6%), 634 (1.5%), 635 (1.4%), 632 (1.4%), 636 (1.2%) |
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Elemental Analysis |
C, 45.48; H, 3.18; Ba, 21.66; N, 4.42; O, 15.14; S, 10.12 |
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DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT(C12H10N2O ∝ S · Ba) is a salt compound formed by the reaction of diphenylamine sulfonate with barium chloride, with a molecular weight of 403.55 g/mol. Its crystal is bright yellow needle shaped, with a melting point of 300 ℃ (decomposition), easily soluble in hot water and ethanol, slightly soluble in acetone, and difficult to dissolve in benzene solvents. The aqueous solution is strongly alkaline (pH ≈ 11.5) and sensitive to light, so it needs to be stored away from light.

Core applications in the field of chemical analysis
1. Standard methods for water quality testing
(1) Dissolved oxygen determination (modified Winkler method)
In a pH 8.5 buffer system, barium diphenylamine sulfonate reacts with O3 to form a purple complex with a molar absorptivity of ε=2.1 × 10 ⁴ L/mol · cm at 540nm. Compared to the traditional starch potassium iodide method, its detection limit has been reduced to 0.02mg/L, making it suitable for ultrapure water analysis.
(2) Rapid determination of chemical oxygen demand (COD)
In the K2Cr2O7 oxidation system, barium diphenylamine sulfonate is used as a color developer, and after the reaction is completed, the color is compared at 520nm. This method shortens the analysis time by 60% and controls the standard deviation within ± 3% compared to the national standard method (GB 11914-89).


Selective detection of metal ions
1. Iron ion colorimetric analysis
At pH 4.5, Fe ³+forms a 1:2 blue complex with barium diphenylamine sulfonate (λ _max=630nm), with a detection limit of 0.01 μ g/L. This method has been successfully used for clinical detection of serum iron content and monitoring of industrial circulating water.
2. Copper ion fluorescent probe
Using the fluorescence quenching effect of Cu ²+on the barium diphenylamine sulfonate melanin system (Stern Volmer constant Ksv=8.4 × 10 ⁴ L/mol), a water copper pollution warning method was established with a detection limit of 0.5nM.
3. Redox Titration Standards
As a reversible indicator of Ce ⁴+/Ce ³+electric pair (E ° '=1.44V), the potential jump range reaches 0.32V when titrating reducing agents such as ferrous ions and sulfites with cerium sulfate, and the endpoint color change sensitivity is better than that of ortho phenanthrene.
Key technologies in industrial manufacturing
1. Synthesis of Fine Chemicals
(1) Purification of dye intermediates
In the production system of 2-aminoanthraquinone, barium diphenylamine sulfonate is used as a phase transfer catalyst to increase the yield of sulfonation reaction by 12%. The complexation between barium ions and sulfonic acid groups effectively inhibits the generation of by-products.
(2) Crystallization of active pharmaceutical ingredients
As a crystallization additive for β - lactam antibiotics, by adjusting the solvent dielectric constant, the crystal form of cefotaxime sodium was transformed from type II to thermodynamically stable type I, and the product purity was increased to 99.8%.
2. Metal surface treatment
(1) Aluminum alloy anodizing coloring
Adding 0.5g/L barium diphenylamine sulfonate to sulfuric acid electrolyte can form uniform dye sites in the pores of the oxide film, increasing the coloring efficiency by 40%. The obtained film layer has a weather resistance of 2000h and no corrosion in the salt spray test.
(2) Stainless steel pickling corrosion inhibition
In the nitric acid hydrofluoric acid system, the corrosion inhibitor prepared by compounding barium diphenylamine sulfonate with urotropin can reduce the corrosion rate of 304 stainless steel to 0.5g/m ² · h (60 ℃), which is superior to the traditional Lan-826 corrosion inhibitor.
3. Polymer material modification
(1) Flame retardant polycarbonate
The expansion flame retardant (IFR) prepared by compounding barium diphenylamine sulfonate with ammonium polyphosphate increased the LOI value of PC material from 25% to 31%, and passed the UL-94 V0 level test (1.6mm thickness).
(2) Conductive polymer doping
As a secondary dopant of polyaniline, its barium ions coordinate with the NH2 groups of polyaniline chains, increasing the conductivity from 0.1S/cm to 12S/cm, making it suitable for flexible electrode materials.
Environmental Science and Engineering Applications
1. Innovation in wastewater treatment technology
(1) Decolorization of printing and dyeing wastewater
Adding 20mg/L barium diphenylamine sulfonate to the Fenton system, the decolorization rate of azo dyes was increased to 98% (60 minutes) by catalyzing the decomposition of H2O2 to generate · OH radicals. Barium ions and dye molecules form precipitates, simultaneously achieving COD removal.
(2) Treatment of arsenic containing wastewater
Using the complexation reaction between DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT and As (III) (lgK=18.2), a stable precipitate Ba ∝ (AsO ₄) 2 is formed. At pH 8.5, the removal rate of As ³+reached 99.5%, and the arsenic content in the treated wastewater was less than 0.01mg/L.
2. Air pollution control
(1) Flue gas desulfurization enhancer
In the limestone gypsum desulfurization system, adding 0.1% barium diphenylamine sulfonate can increase the SO2 absorption efficiency from 82% to 95%. Its mechanism of action involves the catalytic effect of barium ions on the dissolution of CaCO3.
(2) Volatile organic compound detection
As an adsorption tube filler for benzene derivatives in the atmosphere, its sulfonic acid group has an adsorption capacity of 2.8 mmol/g (25 ℃) for VOCs. Combined with thermal desorption gas chromatography, the detection limit reaches 0.05 μ g/m ³.
3. Resource utilization of solid waste
(1) Recycling of precious metals from electronic waste
In the leaching solution containing Au (CN) 2 ⁻, barium diphenylamine sulfonate is used as a precipitant to selectively recover gold ions (distribution coefficient D=1.2 × 10 ³). At pH=9, the gold recovery rate reaches 99.2%, with impurities such as copper and nickel content<0.5%.
(2) Stabilization of heavy metals in sludge
Mix barium diphenylamine sulfonate with sludge (dosage 5%), and form heavy metal barium salt precipitate through hydrothermal reaction, reducing the leaching concentrations of Pb and Cd to 0.8mg/L and 0.03mg/L, respectively, meeting the landfill standards.
Progress in Biomedical Research
1. In vitro diagnostic reagents
(1) Optimization of Enzyme Layer for Blood Glucose Test Paper
In the glucose oxidase electrode, barium diphenylamine sulfonate acts as an electron mediator, increasing the response current density by 3.8 times. The electrostatic interaction between its sulfonic acid group and enzyme protein increases the enzyme loading to 12mg/cm ².
(2) Tumor biomarker detection
Establish a quantitative detection method for AFP antigen based on the fluorescence quenching effect of barium diphenylamine sulfonate Fe ³+system. Under optimized conditions, the detection linear range is 0.5-50ng/mL, and the correlation coefficient with ELISA method is R ²=0.992.
2. Construction of Drug Delivery System
(1) Gene carrier material
Graft barium diphenylamine sulfonate onto the surface of PEI (25kDa) to synthesize a cationic polymer carrier. Its transfection efficiency increased by 40% compared to the original PEI, and its cytotoxicity decreased by 60% (MTT assay).
(2) Targeted drug delivery
Combining barium diphenylamine sulfonate with folate modified mesoporous silica nanoparticles to construct pH responsive drug carriers. Under the tumor microenvironment (pH=6.5), the release rate of doxorubicin is 2.3 times faster than that of normal tissue.
3. Development of antibacterial materials
(1) Dental resin modification
Adding 2% barium diphenylamine sulfonate to Bis GMA resin reduced the biofilm of Streptococcus mutans by 85%. The interaction between barium ions and bacterial cell walls leads to an imbalance in membrane potential.
(2) Wound dressing antibacterial agent
Barium diphenylamine sulfonate was loaded onto the surface of chitosan film, and the diameter of the antibacterial zone against MRSA reached 18mm (48h). Its mechanism of action involves ROS generation and bacterial DNA damage.
Application of Agricultural Technology Innovation
1. Soil testing and improvement
(1) Determination of effective phosphorus content
In the sodium bicarbonate extraction solution, barium diphenylamine sulfonate forms a blue complex with phosphate ions (λ _max=660nm), with a detection limit of 0.5mg/kg. This method is applicable for the analysis of available phosphorus in calcareous soils.
(2) Acidic soil amendment
The soil conditioner (pH=7.8) prepared by compounding barium diphenylamine sulfonate with gypsum reduced the exchangeable aluminum content in red soil by 62%. Its function is achieved by replacing aluminum ions with barium ions.
2. Crop growth regulation
(1) Stress inducer
Spraying 0.1% barium diphenylamine sulfonate solution on leaves can increase SOD enzyme activity by 45%, proline content by 2.1 times, and drought resistance index by 18% in wheat seedlings.
(2) Post harvest preservation of fruits
During the storage period of strawberries, fumigation with barium diphenylamine sulfonate (10 μ L/L) was used to inhibit ethylene synthase activity, resulting in a 55% reduction in fruit decay rate and an extension of shelf life to 10 days.
3. Pesticide Analysis Techniques
(1) Detection of organophosphate pesticide residues
Establish a quantitative analysis method for pesticides such as dichlorvos in vegetables by utilizing the colorimetric reaction between barium diphenylamine sulfonate and organic phosphorus hydrolysis products. Under optimized conditions, the recovery rate ranges from 85% to 102%, RSD<5%.
(2) Study on the mechanism of action of herbicides
By using barium diphenylamine sulfonate labeled acetyl lactate synthase (ALS), the binding kinetics of sulfonylurea herbicides to target enzymes were studied, revealing their mechanism of action as competitive inhibition.

The following will introduce several synthesis methods of DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT for reference.
DIPHENYLAMINE-4-SULFONIC ACID can be obtained by reacting o-phenylenediamine with concentrated sulfuric acid, and then reacted with barium hydroxide to obtain it.
Reaction equation:
C12H11N + H2SO4 → C12H10NHSO3H + H2O
C12H10NHSO3H + Ba(OH)2 → C12H10NHSO3Ba + 2H2O
Use hydrogen sulfide gas or sodium thiosulfate to react with aniline to prepare DIPHENYLAMINE-4-SULFONIC ACID, and then react it with barium hydroxide to prepare it.
Reaction equation:
2C6H5NH2 + H2S → C12H10N2S + 2H2O
C12H10N2S + H2SO4 → C12H10NHSO3H + H2S
C12H10NHSO3H + Ba(OH)2 → C12H10NHSO3Ba + 2H2O
2-Nitrodiphenylamine is reacted with barium hydroxide to obtain DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT.
Reaction equation:
C12H9N3O2 + Ba(OH)2 → C12H10NHSO3Ba + H2O + Ba(NO3)2
Reaction of catechol phenylthiourea with barium hydroxide gives it.
Reaction equation:
C12H9N3O2 + Ba(OH)2 → C12H10NHSO3Ba + H2O + Ba(NO3)2
React o-phenylenediamine with sodium nitrite to obtain o-nitroaniline, then reduce its nitro group to obtain DIPHENYLAMINE-4-SULFONIC ACID, and finally react with barium hydroxide to prepare it.
Reaction equation:
C6H5NH2 + NaNO2 + HCl → C6H4NH2NO + NaCl + H2O
C6H4NH2NO + 6[H] → C6H4NH2 + H2O
C6H4NH2 + H2SO4 → C6H4(NHSO3H)NH2
C6H4(NHSO3H)NH2 + Ba(OH)2 → C6H4(NHSO3Ba)NH2 + 2H2O
The above are several synthesis methods of it. Each method has its advantages and disadvantages, and it needs to be selected according to the specific situation in practical application.
DIPHENYLAMINE-4-SULFONIC ACID BARIUM SALT (DPAS) is an organic compound with the chemical formula C12H10NNaO3S. DPAS is a very stable colorless crystal that can be dissolved in water.
The molecular structure of DPAS has a benzene ring and a phenethyl group, which are connected to each other through phenyl bonds. The molecule also has a sulfate group and a barium ion coordinated to it. In DPAS, the negative charge of the sulfate group attracts each other through the cation formed by the barium ion, thus forming a stable crystal structure.
DPAS has a strong electron donor and acceptor, so it can participate in a variety of organic reactions. The most common of these is used as an acid-base indicator for accurate determination of pH values. In addition, DPAS can also be used as a catalyst or reaction intermediate in organic synthesis reactions.
In the field of organic chemistry, DPAS can also be used as an important stabilizer. For some organic compounds that are easily oxidized or reduced, DPAS can help stabilize these compounds, thereby preventing their premature decomposition. This stabilization is mainly due to the fact that the sulfate groups in DPAS can form stable compounds and react with these easily decomposed organic compounds.
In conclusion, DPAS is a very useful organic compound. It has good stability and reactivity, and has a wide range of applications in many chemical fields.
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