L-lisina monohidrato - Moligand™,≥97% , CAS No.39665-12-8

CAS: 39665-12-8 Cat. No.: S133419 Peso molecular: 164.2 Beilstein Registry Number: 4349963 Número EC: 609-735-7

GRADE & PURITY Moligand™, ≥97%

Synonyms

DTXSID70192769 | 2-methylmercaptoimidazoline hydroiodide | Lysine monohydrate | AKOS005145556 | L-Lysine, hydrate | L-Lysine, hydrate (1:x) | AS-13538 | But-3-ynylamine hydrochloride, AldrichCPR | A824685 | AM81902 | L-Lysine monohydrate, purum, >=98.0% (

Storage

Argón cargado

Shipped In

Normal

Descripción general

Un aminoácido esencial

Specifications

Sinónimos

DTXSID70192769 | 2-methylmercaptoimidazoline hydroiodide | Lysine monohydrate | AKOS005145556 | L-Lysine, hydrate | L-Lysine, hydrate (1:x) | AS-13538 | But-3-ynylamine hydrochloride, AldrichCPR | A824685 | AM81902 | L-Lysine monohydrate, purum, >=98.0% (

Especificaciones y pureza

Moligand™, ≥97%

Mecanismos bioquímicos y fisiológicos

L-(+)Lisina Monohidrato es un aminoácido esencial para la nutrición humana, aunque no es sintetizado por el cuerpo humano.α-aminoácido esencial. Sustrato para estudios de oxidación y mecanismos de glicación. Precursor de acetil-CoA in vivo. Regula la abso

Condiciones de almacenamiento de almacenamiento

Argón cargado

Enviado en

Normal

Grado

Moligand™

Nota

Siempre que sea posible, prepare y utilice las soluciones el mismo día. No obstante, si necesita preparar soluciones madre con antelación, le recomendamos que almacene la solución como alícuotas en viales herméticamente cerrados a -20°C. Por lo general, podrán utilizarse durante un mes. Antes de su uso, y antes de abrir el vial, le recomendamos que deje que el producto se equilibre a temperatura ambiente durante al menos 1 hora. ¿Necesita más consejos sobre solubilidad, uso y manipulación? Visite nuestra página de preguntas frecuentes (FAQ) para obtener más información.

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488199126
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488199126
• Sonrisas canónicas: C(CCN)CC(C(=O)O)N.O
• IUPAC Name: (2S)-2,6-diaminohexanoic acid;hydrate
• InChIKey: HZRUTVAFDWTKGD-JEDNCBNOSA-N
• INCHI: 1S/C6H14N2O2.H2O/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H2/t5-;/m0./s1
• Isómeros SMILES: C(CCN)C[C@@H](C(=O)O)N.O
• WGK Alemania: 3
• Peso molecular: 164.2
• Beilstein: 4349963
• Reaxy-Rn: 13586730
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13586730&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 Alpha amino acids
              • Level8 L-alpha-amino acids

• 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 - Alpha amino acids
• Direct Parent: L-alpha-amino acids
• Alternative Parents: Medium-chain fatty acids Amino fatty acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: L-alpha-amino acid - Medium-chain fatty acid - Amino fatty acid - Fatty acid - Fatty acyl - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Organic nitrogen compound - Amine - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
• 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water (300 g/L).
• Sensibilidad: Air and moisture sensitive
• Rotación específica [α]: +22°,c = 2 in 6 M HCl
• Punto de fusión (°C): 210°C
• Peso molecular: 164.200 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 164.116 Da
• Monoisotopic Mass: 164.116 Da
• Topological Polar Surface Area: 90.300 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 106.000
• 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. Zhang Gaoyu, Sang Laifa, Xu Guogang, Dou Yajie, Wang Xinzhen.  (2020)  Synthesis and characterization of meso-porous Au-modified SnO2 fibers using natural silk with enhanced sensitivity for n-butanol.  JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS,  31  (11): (8220-8229).  [PMID:] [10.1007/s10854-020-03357-z]

2. Shihua Yu, Zhigang Liu, Jianpo Zhang, Hongwei Li, Na Xu, Xin-xin Yuan, Yuqing Wu.  (2018)  An azo-coupling reaction-based surface enhanced resonance Raman scattering approach for ultrasensitive detection of salbutamol.  RSC Advances,  8  (10): (5536-5541).  [PMID:35542390] [10.1039/C7RA12927K]