L-Lysine monohydrate - Animal Free,BioReagent,for cell culture,Moligand™ , CAS No.39665-12-8

CAS: 39665-12-8 Cat. No.: L478519 Formula: C₆H₁₄N₂O₂ · H₂O Peso molecolare: 164.2 Beilstein Registry Number: 4349963 Numero EC: 609-735-7

GRADE & PURITY Animal Free, BioReagent, Moligand™, for Cell culture

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

Room temperature

Panoramica

L-Lysine is an amino acid with a basic side chain and is amphipathic in nature. It has a protonated alkyl amino group and is fully protonated at physiological pH. L-lysine mainly participates in electrostatic interactions in proteins.L-Lysine monohydrate has been used in:SILAC (stable isotope labeling by amino acids in cell culture) methodthe complete synthetic (C) medium for positive selection screening of yeast cellsthe growth medium for cells

Specifications

Sinonimi

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% (

Specifiche e purezza

Animal Free,BioReagent,for cell culture,Moligand™

Meccanismi biochimici e fisiologici

L-Lysine is an essential proteinogenic α amino acid used in a wide range of applications including as a non-animal sourced supplement in cell culture media, a substrate of enzymes such as L-lysine oxidase (EC 1.4.3.14), a component of poly-lysine polymers

Condizioni di conservazione di stoccaggio

Room temperature

Grado

Animal Free, BioReagent, Moligand™, per la coltura cellulare

Nomi e identificatori

Pubchem Sid

504768144

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504768144

Sorrisi canonici

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

Isomeri SMILES

C(CCN)C[C@@H](C(=O)O)N.O

WGK Germania

3

Peso molecolare

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
    • Classe 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
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Solubilità: H2O: soluble
• Rotazione specifica [α]: +22°,c = 2 in 6 M HCl
• Punto di fusione (°C): 210°C
• Peso molecolare: 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

Domande frequenti

What does Animal Free mean?

Animal Free indicates that the material has been processed and tested for specialty industrial processing. Specifications focus on the impurities that affect performance in that application — for example, metal content for electronics, particle size for batteries, refractive index for optics, or moisture content for moisture-sensitive processes.

What does BioReagent mean?

BioReagent indicates that the product has been processed and tested for biological and biochemical applications. Specifications may include endotoxin limits, microbial controls, sterility, low DNase/RNase/protease activity, and verified biological activity where relevant.

How should this product be stored?

Store at room temperature.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 39665-12-8, the molecular formula is C6H16N2O3, and the molecular weight is 164.2 g/mol. InChIKey HZRUTVAFDWTKGD-JEDNCBNOSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.