Skip to main content

L-methionine sulfoximine

ADVERTISEMENT
Identification
Molecular formula
C5H12N2O3S
CAS number
2312-35-8
IUPAC name
2-amino-4-(methylsulfonimidoyl)butanoic acid
State
State

At room temperature, L-methionine sulfoximine is in a solid state.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
405.00
Boiling point (Kelvin)
678.15
General information
Molecular weight
182.23g/mol
Molar mass
182.2320g/mol
Density
1.4440g/cm3
Appearence

L-methionine sulfoximine typically appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of 2-amino-4-(methylsulfonimidoyl)butanoic acid

The solubility of 2-amino-4-(methylsulfonimidoyl)butanoic acid can be greatly influenced by various factors, including temperature, pH, and the presence of other solutes. Here are some key points regarding its solubility:

  • Polar Nature: Due to the presence of the amino group (-NH2) and the sulfonimidoyl group (-S(=O)2NR2), this compound exhibits a polar character that generally enhances its solubility in polar solvents such as water.
  • pH Dependence: The solubility may vary significantly with changes in pH, as the amino acid nature can lead to protonation or deprotonation, affecting its solubility dynamics. In more acidic or basic conditions, its ability to form ionized species can increase solubility.
  • Hydrogen Bonding: The potential for hydrogen bonding, owing to functional groups present, can facilitate solvation in aqueous environments, further enhancing solubility.
  • Temperature Effects: Typically, an increase in temperature may also increase the solubility of organic compounds, suggesting that temperature control may be significant while handling this substance.

In conclusion, the solubility of 2-amino-4-(methylsulfonimidoyl)butanoic acid is multifaceted, relying on its molecular structure and the environmental conditions of the solution. As with many chemical compounds, comprehending these interactions can lead to a better understanding of its behavior in different solvents.

Interesting facts

Interesting Facts about 2-amino-4-(methylsulfonimidoyl)butanoic acid

2-amino-4-(methylsulfonimidoyl)butanoic acid, often referred to in the scientific community for its unique structural features, is an organic compound that plays a significant role in biochemical research and applications. Here are some intriguing aspects of this compound:

  • Biological Importance: This compound contains an amino group, making it a part of the family of amino acids. Amino acids are vital for various biological processes, including protein synthesis, making this compound important in metabolic pathways.

  • Functionality: The methylsulfonimidoyl group is particularly interesting as it contributes to the compound's reactivity and potential applications in synthetic chemistry. Compounds with sulfonimidoyl groups often exhibit unique properties that can be harnessed for developing pharmaceuticals.

  • Potential Therapeutic Applications: Research indicates that amino acids with sulfonimidoyl functionalities can exhibit antimicrobial and antitumor properties. This opens possibilities for 2-amino-4-(methylsulfonimidoyl)butanoic acid in drug development.

  • Synthesis: The synthesis of this compound can involve multiple organic reactions, incorporating protective groups to manipulate functional groups effectively. Chemists often find this compound intriguing due to the challenges and creativity involved in its synthesis.

  • Analytical Techniques: Studies involving this compound typically utilize sophisticated analytical techniques such as NMR spectroscopy and mass spectrometry, allowing for detailed analysis of its structure and behavior under various conditions.

In conclusion, 2-amino-4-(methylsulfonimidoyl)butanoic acid is not just an ordinary amino acid but a compound that embodies the complexity and beauty of organic chemistry. Its unique structure and potential applications in different fields make it a subject of ongoing research and fascination.

Synonyms
METHIONINE SULFOXIMINE
1982-67-8
2-Amino-4-(S-methylsulfonimidoyl)butanoic acid
DL-Methionine-DL-sulfoximine
2-Amino-4-(S-methylsulphonimidoyl)butyric acid
2-amino-4-(methylsulfonimidoyl)butanoic acid
CHEBI:47833
l-methionine-dl-sulfoximine
Methionine-DL-sulfoximine, DL-
(2S)-2-AMINO-4-(METHYLSULFONIMIDOYL)BUTANOIC ACID
DL-Methionine DL-sulfoximine
DL-METHIONINE SULFOXIMINE
L-Methionine-RS-sulfoximine
DL-(3-Amino-3-carboxypropyl) methyl sulfoximine
SCHEMBL187873
L -S-(3-Amino-3-carboxypropyl)-S-methylsulfoximine
CHEMBL1615096
Sulfoximine, S-(3-amino-3-carboxypropyl)-S-methyl-, DL-
NSC49169
CCG-42326
MFCD00063094
NSC-49169
STK501262
AKOS005171800
FM57660
SB33993
DB-269635
CS-0449453
NS00046662
2-Amino-4-(S-methylsulfonimidoyl)butanoicacid
EN300-373833
G31982
2-Amino-4-(S-methylsulfonimidoyl)-Butanoic acid
AE-641/01924064
SR-01000632335-1
Q27120816
S-(3-Amino-3-carboxypropyl)-S-methyl-DL-Sulfoximine
S-(3-Amino-3-carboxypropyl)-S-methylsulfoximine, 9CI
2-amino-4-[imino(methyl)oxo-lambda6-sulfanyl]butanoic acid
Butanoic acid, 2-amino-4-(S-methylsulfonimidoyl)- (9CI)