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Methionine

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Identification
Molecular formula
C5H11NO2S
CAS number
63-68-3
IUPAC name
2-formamido-4-methylsulfanyl-butanoic acid
State
State

Solid at room temperature

Melting point (Celsius)
281.00
Melting point (Kelvin)
554.15
Boiling point (Celsius)
267.00
Boiling point (Kelvin)
540.15
General information
Molecular weight
149.21g/mol
Molar mass
149.2110g/mol
Density
1.3400g/cm3
Appearence

Form: Crystalline solid

Color: White or off-white

Comment on solubility

Solubility of 2-formamido-4-methylsulfanyl-butanoic acid (C5H11NO2S)

The solubility of 2-formamido-4-methylsulfanyl-butanoic acid in various solvents is influenced by its unique chemical structure. Understanding its solubility can provide insight into its potential applications in biological and chemical processes.

Key Points on Solubility:

  • Aqueous Solubility: 2-formamido-4-methylsulfanyl-butanoic acid is expected to exhibit moderate solubility in water due to the presence of both amide and carboxylic acid functional groups, which can engage in hydrogen bonding with water.
  • Solvent Variability: Its solubility can change significantly depending on the pH of the solution. At acidic pH levels, the carboxylic acid may remain protonated, potentially altering solubility attributes.
  • Organic Solvents: In organic solvents, the solubility may vary. Polar organic solvents like ethanol or methanol could show better compatibility compared to non-polar solvents.

In summary, the complexity of 2-formamido-4-methylsulfanyl-butanoic acid results in variable solubility characteristics influenced by solvent type and environmental conditions. Determining the precise solubility can aid in maximizing its effectiveness in applications ranging from pharmaceuticals to biochemical research.

Interesting facts

Interesting Facts about 2-formamido-4-methylsulfanyl-butanoic Acid

2-formamido-4-methylsulfanyl-butanoic acid, a compound that may not be widely recognized outside of specialized chemistry circles, is indeed a fascinating compound. It showcases intriguing characteristics that highlight the complexity and diversity of organic compounds. Here are some noteworthy points:

  • Biological Significance: This compound plays a role in the biosynthesis of certain amino acids and can be related to various metabolic pathways, showcasing the interconnectedness of biochemical systems.
  • Functional Groups: The presence of both a formamido group and a methylsulfanyl group contributes to its unique reactivity, making it of interest in synthetic chemistry as a potential building block for more complex molecules.
  • Potential Applications: Due to its structure, 2-formamido-4-methylsulfanyl-butanoic acid may serve as a lead compound in drug discovery, especially in the development of pharmaceuticals targeting metabolic disorders.
  • Research Interest: Researchers are keen on understanding its interaction mechanisms, which can help in the design of inhibitors for specific enzymes, further promoting advances in medicinal chemistry.

As a compound rich in potential, 2-formamido-4-methylsulfanyl-butanoic acid exemplifies how even relatively simple molecules can have profound implications in both biological contexts and synthetic applications. The exploration of such compounds underscores the creativity and innovation that characterizes the field of chemistry.

Synonyms
N-Formyl-DL-methionine
For-DL-Met-OH
4309-82-4
2-formamido-4-methylsulfanylbutanoic acid
EINECS 224-322-8
DL-Methionine, N-formyl-
MFCD00063284
NSC 206506
2-Formylamino-4-methylsulfanyl-butyric acid
Butanoic acid, 2-formylamino-4-methylthio-
N-Formyl methionine
MFCD00021033
N-Formyl(methyl)homocysteine #
NSC-334322
Formyl-DL-methionine
Methionine,N-formyl-
N-For-Met-OH
SCHEMBL38594
CHEBI:182822
NSC206506
NSC334322
AKOS009159215
NSC-206506
2-ormamido-4-methylsulanylbutanoic acid
AS-56515
FF107896
SY052429
SY066222
CS-0188321
F0123
Q307455
224-322-8