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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items DL-Lysine·HCl - BioReagent , CAS No.70-53-1
GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. Synonyms
LYSINE, DL-, HYDROCHLORIDE | Lysine, monohydrochloride | UNII-1J3H6DC5PT | 2,3-Dihydro-5-benzofuranaceticAcid | AM20100661 | 1J3H6DC5PT | 81478P92RJ | DL-LYSINE HYDROCHLORIDE | DL-Lysine monohydrochloride | FT-0627946 | Lysine hydrochloride, DL- | DL-2,6-
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Why this grade BioReagent BioReagent for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
LYSINE, DL-, HYDROCHLORIDE | Lysine, monohydrochloride | UNII-1J3H6DC5PT | 2, 3-Dihydro-5-benzofuranaceticAcid | AM20100661 | 1J3H6DC5PT | 81478P92RJ | DL-LYSINE HYDROCHLORIDE | DL-Lysine monohydrochloride | FT-0627946 | Lysine hydrochloride, DL- | DL-2, 6-
Especificaciones y pureza
BioReagent
Mecanismos bioquímicos y fisiológicos
DL-Lysine monohydrochloride is a racemic mixture of the D- and L- enantiomers of lysine. DL-Lysine can be used to construct polylysine polymers that can be used to produce lysine-based peptide gels and films.
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488181520 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181520 Sonrisas canónicas C(CCN)CC(C(=O)O)N.Cl IUPAC Name 2,6-diaminohexanoic acid;hydrochloride InChIKey BVHLGVCQOALMSV-UHFFFAOYSA-N INCHI 1S/C6H14N2O2.ClH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H Isómeros SMILES C(CCN)CC(C(=O)O)N.Cl WGK Alemania 3 Peso molecular 182.65 Reaxy-Rn 4153968 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4153968&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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 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 Alpha-amino acid - Medium-chain fatty acid - Amino fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrochloride - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). 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.
Estructura 3D Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in water. Insoluble in ethanol, ethyl ether, acetone, benzene and common neutral solvents. Punto de fusión (°C) 267°C Peso molecular 182.650 g/mol XLogP3 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 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
Calculadoras de soluciones Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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Reconstitution Calculator Reseñas Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View BioReagent grade guide →
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