p-Aminobenzenesulfonic acid Sulfanilic acid

Published by BDMAEE on 2024-01-22 | Permalink

Structural formula

Business number	03DS
Molecular formula	C6H7NO3S
Molecular weight	173.19
label	sulfamate, Para-aminobenzenesulfonic acid, 4-aminobenzenesulfonic acid, p-Aminobenzenesulfonic acid, anhydrous, Anhydrous p-aminobenzene sulfonic acid, Para-aminobenzenesulfonic acid (anhydrous), Anhydrous 4-aminobenzenesulfonic acid, Aniline-4-sulfonic acid, Aniline-4-sulfonic acid, Aniline p-sulfonic acid, 4-Sulfoaniline, 4-Aminobenzenesulphonic acid, 4-Anilinesulfonic acid, Sulphanilic acid, Sulfanilsaeure, whitening agent, Fungicide

Numbering system

CAS number:121-57-3

MDL number:MFCD00007886

EINECS number:204-482-5

RTECS number:WP3895500

BRN number:908765

PubChem ID:None

Physical property data

1. Properties: White crystalline powder. It changes color easily when exposed to light. Hydrates lose water at 100°C, and anhydrous substances begin to decompose and carbonize at 280°C.

2. Density (g/mL, 25/4℃): 1.485

3. Relative vapor density (g/mL, air=1): Undetermined

4. Melting point (ºC): 288

5. Boiling point (ºC, normal pressure): Undetermined

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined

10. Autoignition point or ignition temperature (ºC): Undetermined

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V /V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Slightly soluble in cold water, soluble in ethanol.�Ammonia, carbonate, alkali metal hydroxide solution, ether and benzene are significantly acidic and can be dissolved in caustic soda solution and sodium carbonate solution.

Toxicological data

1. Acute toxicity: Rat oral LD50: 12300mg/kg Rat intravenous LD50: 6gm/kg

2. Mouse Oral LC50: >3200mg/kg. Harmful if ingested, inhaled or absorbed through the skin. Has a stimulating effect.

Ecological data

None

Molecular structure data

1. Molar refractive index: 40.71

2. Molar volume (cm³/mol): 114.4

3. Isotonic specific volume (90.2K ): 328.2

4. Surface tension (dyne/cm): 67.5

5. Dielectric constant:

6. Dipole moment (10^-24cm³):

7. Polarizability: 16.14

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -0.6

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 1

5. Number of tautomers:

6. Topological molecular polar surface area (TPSA): 80.4

7. Number of heavy atoms: 11

8. Surface charge: 0

9. Complexity: 211

10. Number of isotope atoms : 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the chemical bond configuration Number of centers: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Acidic and irritating. It decomposes when heated and releases toxic gases such as nitrogen and sulfur oxides. Decomposes upon exposure to light.

2. Harmful if inhaled, taken orally or in contact with skin. Avoid contact with eyes when using.

Storage method

Stored in a cool, dry place. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. They should be stored separately from oxidants, acids, and alkalis, and avoid mixed storage.

Synthesis method

1. Obtained from the reaction of aniline and sulfuric acid to form a salt and then translocation.

2.Put aniline dropwise into concentrated sulfuric acid to react, and pour the reaction mixture into cold water to obtain a colorless precipitate of p-aminobenzenesulfonic acid. After cooling, filter and dry to obtain p-aminobenzene sulfonic acid.

3.Water recrystallization and purification.
4. It can be obtained by reacting aniline and sulfuric acid to form a salt and transposition:

Purpose

1. Used in the manufacture of azo dyes, etc., and also used as pesticides to prevent and control wheat rust.

2. Mainly used in the manufacture of dyes, printing and dyeing auxiliaries, prevention and control of wheat rust, and as spices, Intermediates for food pigments, medicines, whitening agents, pesticides, etc.

3. Used in organic synthesis, and also used as chromatography reagents, etc.

4. Used as benchmark reagents , experimental reagents and chromatographic analysis reagents.

5.Benchmark reagents. Determination of aluminum, magnesium, potassium, sodium, iodine, iodide and nitrite. Used together with 1-naphthylamine to determine nitrite and test osmium and ruthenium. Potassium can be measured indirectly through potassium nitrite. Determination of serum bilirubin, soil analysis. It is also used in printing and dyeing auxiliaries, pesticides and fungicides, spices, food pigments, pharmaceuticalbuildingmaterials and other fields. span>

6.Used as an analytical reagent, such as a reference reagent for the determination of nitrite. It is also used as chromatographic analysis reagent, dye synthesis and pharmaceutical industry.