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Sulfanilic acid

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Identification
Molecular formula
C6H7NO3S
CAS number
121-57-3
IUPAC name
2-aminobenzenesulfonic acid
State
State

At room temperature, sulfanilic acid is typically in a solid state. It exists as a crystalline powder, usually stable under normal conditions.

Melting point (Celsius)
288.00
Melting point (Kelvin)
561.00
Boiling point (Celsius)
291.00
Boiling point (Kelvin)
564.00
General information
Molecular weight
173.19g/mol
Molar mass
173.1940g/mol
Density
1.4850g/cm3
Appearence

Sulfanilic acid appears as a white or slightly gray crystalline solid. It may also appear as powder-like granules. The compound is known to be slightly hygroscopic, meaning it can absorb moisture from the environment. When it absorbs moisture, its appearance may change slightly, tending towards a glossier or more translucent form.

Comment on solubility

Solubility of 2-Aminobenzenesulfonic Acid

2-Aminobenzenesulfonic acid, also known as sulfanilic acid, displays interesting solubility characteristics that contribute to its applications in various fields.

One of the key aspects of its solubility is:

  • Water Solubility: 2-aminobenzenesulfonic acid is notably soluble in water due to the presence of the sulfonic acid group (-SO3H), which enhances its ionic potential.
  • Temperature Dependency: Its solubility can increase with temperature, making it more soluble in warm conditions compared to cold.
  • pH Influence: The solubility is also affected by the pH of the solution. In more acidic environments, it remains protonated, while in neutral or alkaline conditions, it may deprotonate, further enhancing solubility.

To quote a common observation, "The greater the number of polar functional groups, the higher the solubility in polar solvents," and 2-aminobenzenesulfonic acid exemplifies this beautifully through its behavior in aqueous solutions.

Overall, 2-aminobenzenesulfonic acid demonstrates a robust solubility profile, paving the way for its widespread use in dyes and pharmaceuticals.

Interesting facts

Interesting Facts about 2-Aminobenzenesulfonic Acid

2-Aminobenzenesulfonic acid, commonly known as o-aminobenzenesulfonic acid or orthanilic acid, is an intriguing compound with a variety of applications in the field of chemistry and beyond. Here are some captivating insights about this compound:

  • Structure and Properties: 2-Aminobenzenesulfonic acid features both an amino group and a sulfonic acid group attached to a benzene ring, which contributes to its unique reactivity and solubility characteristics.
  • Biological Significance: This compound plays an important role in biochemistry; it is used as a reagent in various reactions, particularly those involving diazotization, a reaction essential for synthesizing dyes and pigments.
  • Applications: 2-Aminobenzenesulfonic acid is widely employed in the development of:
    • Photoactive materials
    • Dyes and pigments in the textile industry
    • Pharmaceuticals, particularly in drug development due to its versatility.
  • Environmental Relevance: The compound's sulfonic acid group makes it polar, enhancing its reactivity towards pollutants, and allowing it to be utilized in various environmental remediation processes.
  • Historical Context: Its derivatives have been part of research since the early 20th century, underscoring its long-standing importance in synthetic organic chemistry.

As a compound with dual functionality, 2-aminobenzenesulfonic acid not only serves as a building block in synthetic chemistry but also bridges the gap between organic chemistry and environmental science. Its multifaceted nature invites continual exploration in both academic and industrial laboratories.

In summary, 2-aminobenzenesulfonic acid exemplifies how a simple molecular structure can lead to diverse applications across various fields, showcasing the beauty and complexity of chemical compounds.

Synonyms
2-Aminobenzenesulfonic acid
88-21-1
Orthanilic acid
Aniline-2-sulfonic acid
o-Aminobenzenesulfonic acid
o-Sulfanilic acid
2-Aminobenzenesulphonic acid
Aniline-o-sulfonic acid
2-Sulfanilic acid
Aniline-o-sulphonic acid
1-Aminobenzene-2-sulfonic acid
Benzenesulfonic acid, 2-amino-
Benzenesulfonic acid, o-amino-
Anilino-o-sulfonic acid
Anilino-2-sulfonic acid
Anilino-o-sulphonic acid
2-amino-benzenesulfonic acid
o-Aminophenylsulfonic acid
NSC 147
CCRIS 4575
aniline-2-sulphonic acid
2-Sulfoaniline
ZB9JSA4BH0
EINECS 201-810-9
O-ANILINESULFONIC ACID
CHEBI:1015
2-aminobenzene-1-sulfonic acid
DTXSID1024463
2-anilinesulfonic acid
AI3-52212
NSC-147
MFCD00007705
ORTHANILIC ACID [MI]
DTXCID204463
EC 201-810-9
AMINOBENZENESULFONIC ACID, 2-
UNII-ZB9JSA4BH0
2-Aminobenzene sulfonic acid
2Sulfoaniline
oSulfanilic acid
2-sulfo-aniline
2Sulfanilic acid
o-sulphanilic acid
Aniline-2-sulfonate
Anilineosulfonic acid
Anilinoosulfonic acid
oAnilinesulfonic acid
ortho-sulfanilic acid
2Anilinesulfonic acid
Aniline2sulfonic acid
Anilino2sulfonic acid
Anilineosulphonic acid
Anilinoosulphonic acid
Aniline2sulphonic acid
oAminophenylsulfonic acid
2Aminophenylsulfonic acid
aminobenzenesulphonic acid
Orthanilic acid (Aniline-2-sulfonic acid)
oAminobenzenesulfonic acid
2-Aminobenzenesulfonicacid
2Aminobenzenesulfonic acid
2Aminobenzenesulphonic acid
bmse000766
1Aminobenzene2sulfonic acid
2Aminobenzene sulfonic acid
Benzenesulfonic acid, oamino
oAmino benzene sulfonic acid
Benzenesulfonic acid, 2amino
SCHEMBL90023
NSC147
1-aminobenzene-2-sulphonic acid
Aniline-2-sulfonic acid, 95%
CHEMBL1372690
2-AMINOPHENYLSULFONIC ACID
Tox21_200956
O-AMINO BENZENE SULFONIC ACID
s6032
STL163408
AKOS000299114
CS-W016018
HY-W015302
CAS-88-21-1
NCGC00091721-01
NCGC00091721-02
NCGC00258509-01
AC-11378
TS-00165
DB-057050
A0266
NS00002203
EN300-79575
C06333
D71116
Q2031743
F0001-2187
Z1211373913