L-Methionine Methyl Ester Hydrochloride - ≥98% , CAS No.2491-18-1

CAS: 2491-18-1 Cat. No.: M109222 Peso molecular: 199.7 Beilstein Registry Number: 3913214 Número EC: 219-651-9

GRADE & PURITY ≥98%

Synonyms

H-Met-OMe hydrochloride | L-METHIONINE METHYL ESTER HCl | AC-19226 | MFCD00012491 | MPWSRGAWRAYBJK-UHFFFAOYSA-N | H-Met-OMe.HCl | J-300200 | Methyl 2-amino-4-(methylsulfanyl)butanoate | L-methionine, methyl ester hydrochloride | SCHEMBL200899 | Met-OMe. H

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

H-Met-OMe hydrochloride | L-METHIONINE METHYL ESTER HCl | AC-19226 | MFCD00012491 | MPWSRGAWRAYBJK-UHFFFAOYSA-N | H-Met-OMe.HCl | J-300200 | Methyl 2-amino-4-(methylsulfanyl)butanoate | L-methionine, methyl ester hydrochloride | SCHEMBL200899 | Met-OMe. H

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at -20°C

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488197496
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197496
• Sonrisas canónicas: COC(=O)C(CCSC)N.Cl
• IUPAC Name: methyl (2S)-2-amino-4-methylsulfanylbutanoate;hydrochloride
• InChIKey: MEVUPUNLVKELNV-JEDNCBNOSA-N
• INCHI: 1S/C6H13NO2S.ClH/c1-9-6(8)5(7)3-4-10-2;/h5H,3-4,7H2,1-2H3;1H/t5-;/m0./s1
• Isómeros SMILES: COC(=O)[C@H](CCSC)N.Cl
• WGK Alemania: 3
• CAS alternativo: 10332-17-9
• Peso molecular: 199.7
• Beilstein: 3913214
• Reaxy-Rn: 3913212
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3913212&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Methionine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Methionine and derivatives
• Alternative Parents: Alpha amino acid esters Fatty acid esters Quaternary ammonium salts Methyl esters Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Organic oxides Organic chloride salts Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Methionine or derivatives - Alpha-amino acid ester - Fatty acid ester - Fatty acyl - Quaternary ammonium salt - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Amine - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxide - Organic oxygen compound - Organic chloride salt - Carbonyl group - Organic salt - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (no humanos)

metG Methionyl-tRNA synthetase (123 Activities)

Discover Target: metG

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water.
• Sensibilidad: Hygroscopic
• Rotación específica [α]: [α]D 26° (C=1,H2O)
• Punto de fusión (°C): 150°C
• Peso molecular: 199.700 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 199.043 Da
• Monoisotopic Mass: 199.043 Da
• Topological Polar Surface Area: 77.600 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 108.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Luyao Zheng, Zhiyuan Zhao, Ye Yang, Yaming Li, Chengxiao Wang.  (2020)  Novel skin permeation enhancers based on amino acid ester ionic liquid: Design and permeation mechanism.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:31953082] [10.1016/j.ijpharm.2020.119031]