L-(+)-Lysine Monohydrochloride - Animal Free, USP, JP, Ph.Eur., for cell culture, ≥98.5% , CAS No.657-27-2

CAS: 657-27-2 Cat. No.: L113006 Molecular Weight: 182.65 Beilstein Registry Number: 3563889 EC Number: 211-519-9

GRADE & PURITY Animal Free, USP, JP, Ph.Eur., for Cell culture, ≥98.5%

Synonyms

LYSINE HYDROCHLORIDE (MART.) | Q27124123 | (S)-2,6-Diaminohexanoic acid hydrochloride(1:x) | DTXSID10904868 | NSC760110 | NSC-760110 | H-Lys-OH⋅HCl | L-Lysine-Hydrochloride | lysine hydrochloride | LYSINE HYDROCHLORIDE [USAN] | HY-N0470 | L-Lysine hydroch

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

LYSINE HYDROCHLORIDE (MART.) | Q27124123 | (S)-2, 6-Diaminohexanoic acid hydrochloride(1:x) | DTXSID10904868 | NSC760110 | NSC-760110 | H-Lys-OH⋅HCl | L-Lysine-Hydrochloride | lysine hydrochloride | LYSINE HYDROCHLORIDE [USAN] | HY-N0470 | L-Lysine hydroch

Specifications & Purity

Animal Free, USP, JP, Ph.Eur., for cell culture, ≥98.5%

Biochemical and Physiological Mechanisms

Lysine is a naturally occurring amino acid used in labeling of human bone marrow mesenchymal stem cells for analysis.

Storage

Room temperature

Shipped In

Normal

Grade

Animal Free, for Cell culture, JP, Ph.Eur., USP

Action Type

INHIBITOR

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥98.5%

Names and Identifiers

• Pubchem Sid: 504754410
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754410
• Canonical Smiles: C(CCN)CC(C(=O)O)N.Cl
• IUPAC Name: (2S)-2,6-diaminohexanoic acid;hydrochloride
• InChIKey: BVHLGVCQOALMSV-JEDNCBNOSA-N
• INCHI: 1S/C6H14N2O2.ClH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H/t5-;/m0./s1
• Isomeric SMILES: C(CCN)C[C@@H](C(=O)O)N.Cl
• WGK Germany: 2
• RTECS: OL5650000
• Alternate CAS: 10098-89-2
• Molecular Weight: 182.65
• Beilstein: 3563889
• Reaxy-Rn: 4153968
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4153968&ln=

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 Alpha amino acids
              • Level8 L-alpha-amino acids

• 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 - 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 Hydrochlorides 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 - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Hydrochloride - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aliphatic acyclic compound
• Description: 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: hydrochloride

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

Chemical and Physical Properties

• Solubility: H2O: 100 mg/mL
• Specific Rotation[α]: 20 ° (C=8, HCl (1+1))
• Melt Point(°C): 263 °C
• Molecular Weight: 182.650 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 182.082 Da
• Monoisotopic Mass: 182.082 Da
• Topological Polar Surface Area: 89.300 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

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