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2-Mercaptobenzoic acid

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Identification
Molecular formula
C8H8O2S
CAS number
147-93-3
IUPAC name
2-methylsulfanylbenzoic acid
State
State

At room temperature, 2-Mercaptobenzoic acid is typically found in a solid state.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
371.00
Boiling point (Kelvin)
644.15
General information
Molecular weight
168.21g/mol
Molar mass
168.2050g/mol
Density
1.4510g/cm3
Appearence

2-Mercaptobenzoic acid appears as a white to slightly yellow crystalline powder. It may have a distinct, unpleasant odor reminiscent of sulfur compounds.

Comment on solubility

Solubility of 2-Methylsulfanylbenzoic Acid

2-Methylsulfanylbenzoic acid, with the chemical formula C8H10S and commonly referred to as a thiophenol derivative, displays intriguing solubility characteristics that merit attention.

In general, the solubility of organic compounds like 2-methylsulfanylbenzoic acid can be influenced by several factors:

  • Polarity: The presence of the carboxylic acid group contributes to its **polar nature**, increasing its solubility in polar solvents such as water.
  • Hydrophobic and Hydrophilic Balance: The methylsulfanyl group introduces hydrophobic character, which can lead to limited water solubility. Thus, this compound may exhibit better solubility in organic solvents, such as ethanol or dimethyl sulfoxide (DMSO).
  • Effects of Temperature: As with many organic acids, increased temperature can enhance solubility, particularly in polar solvents.

In practical terms, it is important to note:

  • While the compound is soluble in many organic solvents, care should be taken when attempting to dissolve it in water. Its solubility may vary significantly in aqueous environments.
  • The **dissociation of the carboxylic acid** in water can lead to the formation of ions, which can impact solubility dynamics further.

In conclusion, understanding the solubility of 2-methylsulfanylbenzoic acid is crucial for its applications in various fields, particularly in organic synthesis and industrial processes. A comprehensive grasp of its solubility properties can aid in effective handling and usage of this compound.

Interesting facts

Interesting Facts about 2-methylsulfanylbenzoic acid

2-methylsulfanylbenzoic acid, often referred to as a derivative of benzoic acid, showcases unique properties and applications that intrigue chemists and industry professionals alike. Here are some remarkable facts about this compound:

  • Structural Significance: The presence of the methylsulfanyl group attached to the benzoic acid framework enhances its reactivity and solubility, making it a versatile compound in synthetic chemistry.
  • Biological Activity: Compounds containing methylsulfanyl groups have been studied for their potential biological activities, including antimicrobial and anti-inflammatory properties.
  • Industrial Relevance: 2-methylsulfanylbenzoic acid may serve as a building block in the synthesis of various pharmaceuticals, pesticides, and dyes, showcasing its utility in chemical manufacturing.
  • Analytical Applications: The unique structural features of this compound make it a candidate for use in analytical chemistry, particularly in techniques such as chromatography and spectroscopy.

In the context of environmental chemistry, derivatives of benzoic acid, including 2-methylsulfanylbenzoic acid, are studied for their degradation pathways and impact on ecosystems. Such emphasis highlights the importance of understanding chemical compounds beyond their immediate uses, promoting a sustainable approach in chemical research.

As you delve into the fascinating world of 2-methylsulfanylbenzoic acid, remember: “Understanding the small details can lead to significant advancements in science.” This compound exemplifies how minor modifications in structure can lead to a broad spectrum of biological and industrial applications.

Synonyms
2-(Methylthio)benzoic acid
BENZOIC ACID, o-(METHYLTHIO)-
NSC 218090
NSC 104019
NSC 145347
NSC 151478
NSC 221934
BRN 0972385
DTXSID70190720
4-10-00-00273 (Beilstein Handbook Reference)
DTXCID10113211
630-003-8
inchi=1/c8h8o2s/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5h,1h3,(h,9,10
lwjqgkjczoggpj-uhfffaoysa-n
3724-10-5
2-(Methylsulfanyl)benzoic acid
Benzoic acid, 2-(methylthio)-
2-methylsulfanylbenzoic acid
o-(Methylthio)benzoic acid
2-Methylmercaptobenzoic acid
2-Carboxyphenyl methyl sulfide
MFCD00029934
Acide methyl-S-2-benzoique
2-(Methylthio)benzoicAcid
2-(methylmercapto)benzoic acid
carboxythioanisole
Acide methyl-S-2-benzoique [French]
Enamine_005727
SCHEMBL709788
2-(Methylsulfanyl)benzoic acid #
HMS1410E07
2-(Methylthio)benzoic acid, 97%
ALBB-023339
BBL100116
FD7329
NSC104019
NSC145347
NSC151478
NSC218090
NSC221934
STL511346
AKOS000264449
CS-W017800
FS-1045
NSC-104019
NSC-145347
NSC-151478
NSC-218090
NSC-221934
IDI1_007962
NCGC00337580-01
SY048265
DB-019521
M1953
EN300-17330
AB01328835-02
AA-516/30041011
Z56921447
F2147-1697