(S)-2-Amino-4-(methylthio)butanamide hydrochloride - ≥98% , CAS No.16120-92-6

CAS: 16120-92-6 Cat. No.: S587494 EC Number: 840-274-6 PubChem CID: 18531008

GRADE & PURITY ≥98%

Synonyms

PWCBMJHINDTXGV-WCCKRBBISA-N | L-Methionine amide hydrochloride | H-Met-NH2.HCl | (2S)-2-amino-4-(methylthio)-butanamide, monohydrochloride | H-L-Met-NH2 Hydrochloride | H-MET-NH2 HCL | (2S)-2-Amino-4-methylsulfanyl-butanamide hydrochloride | l-methioninam

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

PWCBMJHINDTXGV-WCCKRBBISA-N | L-Methionine amide hydrochloride | H-Met-NH2.HCl | (2S)-2-amino-4-(methylthio)-butanamide, monohydrochloride | H-L-Met-NH2 Hydrochloride | H-MET-NH2 HCL | (2S)-2-Amino-4-methylsulfanyl-butanamide hydrochloride | l-methioninam

Specifications & Purity

≥98%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

INHIBITOR

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CSCCC(C(=O)N)N.Cl
• IUPAC Name: (2S)-2-amino-4-methylsulfanylbutanamide;hydrochloride
• InChIKey: PWCBMJHINDTXGV-WCCKRBBISA-N
• INCHI: 1S/C5H12N2OS.ClH/c1-9-3-2-4(6)5(7)8;/h4H,2-3,6H2,1H3,(H2,7,8);1H/t4-;/m0./s1
• Isomeric SMILES: CSCC[C@@H](C(=O)N)N.Cl
• PubChem CID: 18531008

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class 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
• Class: 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 amides Fatty amides Primary carboxylic acid amides Sulfenyl compounds Dialkylthioethers Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Methionine or derivatives - Alpha-amino acid amide - Fatty amide - Fatty acyl - Carboxamide group - Primary carboxylic acid amide - Dialkylthioether - Sulfenyl compound - Thioether - Organic oxide - Organic nitrogen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Hydrochloride - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: 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

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Air sensitive；Moisture sensitive
• Melt Point(°C): 220 °C
• Molecular Weight: 184.690 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 184.044 Da
• Monoisotopic Mass: 184.044 Da
• Topological Polar Surface Area: 94.400 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 97.000
• 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