1982-67-8

Basic information

• Product Name: DL-METHIONINE DL-SULFOXIMINE
• Synonyms: DL-[3-AMINO-3-CARBOXYPROPYL]METHYL SULFOXIMINE;DL-BANTHIONINE-DL-SULFOXIMINE;DL-LOBAMINE-DL-SULFOXIMINE;DL-METHIONINE SULFOXIMINE;DL-METHIONINE DL-SULFOXIMINE;DL-METHIONINE-DL-SULPHOXIMINE;AURORA KA-705;2-amino-4-(s-methylsulfonimidoyl)-butanoicaci
• CAS NO: 1982-67-8
• Molecular Formula: C₅H₁₂N₂O₃S
• Molecular Weight: 180.23
• EINECS: 217-845-8
• Product Categories: Amino Acids
• Mol File: 1982-67-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 214-218 °C (decomp)
• Boiling Point: 352.2°Cat760mmHg
• Flash Point: 166.8°C
• Appearance: /
• Density: 1.215 (estimate)
• Vapor Pressure: 6.63E-06mmHg at 25°C
• Refractive Index: 1.6430 (estimate)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: DL-METHIONINE DL-SULFOXIMINE(CAS DataBase Reference)
• NIST Chemistry Reference: DL-METHIONINE DL-SULFOXIMINE(1982-67-8)
• EPA Substance Registry System: DL-METHIONINE DL-SULFOXIMINE(1982-67-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• RTECS: WS3560000
• Hazardous Substances Data: 1982-67-8(Hazardous Substances Data)

Usage

Description

DL-METHIONINE DL-SULFOXIMINE, also known as L-Methionine S,S-dioxide, is a non-proteinogenic alpha-amino acid that is the sulfoximine derivative of methionine. It possesses unique structural properties and is known for its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
DL-METHIONINE DL-SULFOXIMINE is used as a pharmaceutical compound for its potential therapeutic effects. It is being investigated for its ability to modulate certain biological processes and may have applications in the treatment of various diseases.
Used in Research and Development:
In the field of research and development, DL-METHIONINE DL-SULFOXIMINE is used as a chemical probe to study the mechanisms of action of various biological processes. Its unique properties make it a valuable tool for understanding the roles of amino acids and their derivatives in cellular functions.
Used in Chemical Synthesis:
DL-METHIONINE DL-SULFOXIMINE is also used as a synthetic building block in the development of new compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

InChI:InChI=1/C5H12N2O3S/c1-11(7,10)3-2-4(6)5(8)9/h4,7H,2-3,6H2,1H3,(H,8,9)/t4-,11+/m0/s1

Upstream product

• 59-51-8 DL-methionine 
• 859200-50-3 (2-methylsulfanyl-ethyl)-malonic acid 
• 1616972-89-4 tert-butyl 4-(N-cyano-S-methylsulfonimidoyl)-2-[(tert-butoxycarbonyl)amino]butanoate 
• 1616972-91-8 tert-butyl 4-(N-acetyl-S-methylsulfonimidoyl)-2-[(tert-butoxycarbonyl)amino]butanoate 
• 1616972-93-0 tert-butyl 2-[(tert-butoxycarbonyl)amino]-4-(S-methylsulfonimidoyl)butanoate 
• 87173-45-3 2-((1R,4R)-1-Methyl-1,3-dioxo-3,4,5,6-tetrahydro-1λ⁶-[1,2]thiazin-4-yl)-isoindole-1,3-dione 
• 87141-35-3 C₁₃H₁₄N₂O₅S 
• 21056-59-7 L-methionine-S,R-sulfoximine 
• 87173-46-4 2-((1S,4R)-1-Methyl-1,3-dioxo-3,4,5,6-tetrahydro-1λ⁶-[1,2]thiazin-4-yl)-isoindole-1,3-dione 

Downstream Products

• 115453-76-4 pteroyl-S-methylhomocysteine sulfoximine 

Relevant articles and documents

Methionine and buthionine sulfoximines: Syntheses under mild and safe imidation/oxidation conditions

Methionine and buthionine sulfoximines (MSO and BSO) are non-natural amino acids known to inhibit the biosynthesis of glutathione (GSH). The current syntheses of these biologically active molecules involve harsh reaction conditions and the use of hazardou

Studies on nitrogen trichloride-treated prolamines; synthesis of the

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