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Benzene-1,4-diaminosulfonic acid

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Identification
Molecular formula
C7H10N2O2S
CAS number
140-10-3
IUPAC name
acetic acid;4-(aminomethyl)benzenesulfonamide
State
State

At room temperature, the compound is typically found in a solid state, commonly in the form of a crystalline powder, which is stable under standard conditions.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
200.23g/mol
Molar mass
200.2300g/mol
Density
1.3865g/cm3
Appearence

This compound appears as a white to off-white crystalline powder. Its appearance makes it easy to handle in laboratory and industrial settings.

Comment on solubility

Solubility of Acetic Acid; 4-(Aminomethyl)benzenesulfonamide (C7H10N2O2S)

The compound acetic acid; 4-(aminomethyl)benzenesulfonamide exhibits notable solubility characteristics that are influenced by its molecular structure. Understanding its solubility is key for practical applications and theoretical insights.

Key Points on Solubility:

  • Polarity: The presence of both acidic (acetic acid group) and basic (aminomethyl group) functionalities contributes to its overall polarity, enhancing solubility in polar solvents.
  • Water Solubility: This compound is generally soluble in water due to the dual nature of its functional groups which can engage in hydrogen bonding.
  • Solvent Compatibility: It may find compatibility in organic solvents as well, particularly those with polar characteristics.
  • pH Dependency: Solubility can be influenced by the pH of the solution; you may find variations in solubility between acidic and neutral or basic environments.
  • Applications: Understanding solubility is vital when considering its application in pharmaceuticals and biochemistry where aqueous solutions are often required.

In summary, the solubility of acetic acid; 4-(aminomethyl)benzenesulfonamide is a result of its molecular features which enable it to dissolve in various solvents, particularly water, enhancing its utility across multiple fields.

Interesting facts

Interesting Facts about Acetic Acid; 4-(Aminomethyl)benzenesulfonamide

Acetic acid; 4-(aminomethyl)benzenesulfonamide, commonly known within certain chemical circles for its unique structure and applications, embodies a fascinating combination of properties that make it significant in both the laboratory and industry. This compound is a hybrid of acetic acid, known for its pungent odor and distinguishing characteristics, and an aryl sulfonamide, which contributes unique functionalities.

Noteworthy Features:

  • Versatility: The presence of both amino and sulfonamide functional groups endows this compound with remarkable versatility. It can participate in various chemical reactions, making it valuable for synthesizing other complex molecules.
  • Biological Relevance: Compounds containing sulfonamide groups are often exploited for their medicinal properties. This specific structure may exhibit antibacterial and antifungal activities, sparking interest in pharmaceutical research.
  • pH Sensitive: Acetic acid’s chemical behavior as a weak acid influences the compound’s reactivity in different environments, allowing it to function effectively in varied pH conditions.

Many labs utilize this compound for research purposes, specifically in exploring new avenues for drug development. As quoted by a renowned chemist, “The incorporation of amino acids into sulfonamide frameworks can open new pathways to therapeutic innovations.” This highlights the ongoing research and discussions surrounding the potential of such compounds.

In summary, acetic acid; 4-(aminomethyl)benzenesulfonamide stands at the intersection of organic chemistry and biological applications, showcasing the endless potential of chemical compounds in advancing science and technology.

Synonyms
MAFENIDE ACETATE
13009-99-9
Sulfamilon
Winthrocine
UNII-RQ6LP6Z0WY
RQ6LP6Z0WY
alpha-Amino-p-toluenesulfonamide monoacetate
EINECS 235-855-0
4-(Aminomethyl)benzenesulfonamide monoacetate
Mafenide acetate [USP:JAN]
DTXSID00156334
Mafenide acetate (USP:JAN)
MAFENIDE ACETATE (MART.)
MAFENIDE ACETATE [MART.]
MAFENIDE ACETATE (USP-RS)
MAFENIDE ACETATE [USP-RS]
MAFENIDE ACETATE (USP MONOGRAPH)
MAFENIDE ACETATE [USP MONOGRAPH]
DTXCID0078825
235-855-0
4-(AMINOMETHYL)BENZENESULFONAMIDE ACETATE
Mafenide (Acetate)
Benzenesulfonamide, 4-(aminomethyl)-, monoacetate
MFCD00072089
Benzenesulfonamide, 4-(aminomethyl)-, acetate (1:1)
acetic acid;4-(aminomethyl)benzenesulfonamide
Mafatate
Maphenide acetate
Mafenamide acetate
4-(aminomethyl)benzene-1-sulfonamide; acetic acid
4-(aminomethyl)benzenesulfonamide, acetic acid
alpha-Aminotoluene-4-sulphonamide monoacetate
Sulfamylon (TN)
Mafenide acetate salt
p-Toluenesulfonamide, alpha-amino-, monoacetate
SCHEMBL41627
Mafenide acetate (JAN/USP)
MLS000069581
MAFENIDE ACETATE [MI]
MAFENIDE ACETATE [JAN]
HY-B0614AR
Mafenide (Acetate) (Standard)
CHEMBL1201161
MAFENIDE ACETATE [VANDF]
CHEBI:31792
HY-B0614A
MAFENIDE ACETATE [WHO-DD]
HMS2231M06
HMS3259N08
HMS3370M14
HMS5081H14
BCP28537
MSK11369
s3647
SBB080601
MAFENIDE ACETATE [GREEN BOOK]
AKOS000121908
MAFENIDE ACETATE [ORANGE BOOK]
CCG-266920
DS-2178
FA24972
NC00709
AC-22835
SMR000058778
SY107388
4-(Aminomethyl)benzenesulfonamide (acetate)
4-Aminomethylbenzenesulfonamide acetate salt
DB-041939
NS00085140
ST45053309
EN300-30046
D01166
.ALPHA.-AMINO-P-TOLUENESULFONAMIDE MONOACETATE
Q27288250
Z1741980223
4-(Aminomethyl)benzenesulfonamide acetate;Mafenide acetate
Mafenide acetate, United States Pharmacopeia (USP) Reference Standard