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3-(bis(2-hydroxyethyl)sulfamoyl)benzoic acid

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Identification
Molecular formula
C11H15NO5S
CAS number
78475-49-1
IUPAC name
3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid
State
State
The compound is a solid at room temperature, usually presented as a crystalline powder.
Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
365.00
Boiling point (Kelvin)
638.15
General information
Molecular weight
259.27g/mol
Molar mass
259.2710g/mol
Density
1.4900g/cm3
Appearence

This compound appears as a crystalline solid. It is typically a white or off-white in color.

Comment on solubility

Solubility of 3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid

The solubility of 3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid (C11H15NO5S) can be examined through the following key points:

  • Polarity: Given the presence of numerous hydroxyl (–OH) groups and a sulfamoyl (–SO2NH2) group, this compound exhibits a relatively high polarity, which typically enhances solubility in polar solvents.
  • Solvent Compatibility: It is likely to be more soluble in water due to its ability to form hydrogen bonds, thus indicating a preference for aqueous environments over non-polar solvents.
  • Temperature Influence: As with many organic compounds, the solubility could increase with temperature, affecting the compound's saturation levels in solution.
  • pH Dependency: The acid functionality can influence solubility in various pH conditions, potentially protonating or deprotonating depending on the surrounding environment, which could have a significant impact on its overall solubility.

In summary, particularly high water solubility and the dependence on solvent properties and environmental conditions make 3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid an intriguing compound to study within various applications, especially in pharmacological contexts.

Interesting facts

Interesting Facts about 3-[bis(2-hydroxyethyl)sulfamoyl]benzoic Acid

3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid is a fascinating compound with a range of applications in various fields of chemistry and biochemistry. Here are some engaging facts about this intriguing molecule:

  • Functional Versatility: This compound features a sulfonamide functional group, which imparts unique properties, allowing it to be utilized in medicinal chemistry for drug development, especially in the design of antibiotics.
  • Hydrophilic Nature: The presence of two hydroxyethyl groups contributes to its hydrophilicity, enhancing its solubility in water. This feature is particularly beneficial for biological applications where solubility in biological fluids is critical.
  • Role in Biochemistry: Compounds like this one are often studied for their interactions with various biological targets, including enzymes and receptors, making them important in the field of pharmacology.
  • Potential Antimicrobial Activity: The sulfamoyl moiety can exhibit activity against a variety of microbes. Researchers continue to explore its efficacy against resistant strains of bacteria, making it a compound of interest for public health.
  • Applications in Polymer Chemistry: This compound can also serve as a building block for the synthesis of polymers, especially those designed for drug delivery systems, improving the bioavailability of therapeutic agents.

Overall, 3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid is a prime example of how organic chemistry can intersect with numerous scientific domains, highlighting the importance of interdisciplinary research in the pursuit of novel solutions to medical challenges.

Synonyms
3-[bis(2-hydroxyethyl)sulfamoyl]benzoic acid
6628-11-1
NSC60299
CBMicro_036958
Cambridge id 5916749
NCIOpen2_002432
Oprea1_088635
Oprea1_723397
SCHEMBL6671420
DTXSID60274422
NSC-60299
NSC163091
AKOS009143118
NSC-163091
BIM-0037075.P001
SR-01000223215
3-{[bis(2-hydroxyethyl)amino]sulfonyl}benzoic acid
SR-01000223215-1