≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Na-Methyl-L-lysine hydrochloride is a versatile amino acid derivative that plays a significant role in various biochemical applications. This compound is recognized for its unique properties, including its ability to act as a methyl donor, which is crucial in numerous enzymatic reactions. Researchers and industry professionals utilize Na-Methyl-L-lysine hydrochloride in the synthesis of peptides and proteins, enhancing the functionality and stability of these biomolecules. Its application extends to the fields of pharmaceuticals, where it is used in drug formulation and development, particularly in the design of therapeutics that require precise amino acid modifications.
Additionally, Na-Methyl-L-lysine hydrochloride is valuable in nutritional studies and metabolic research, where it aids in understanding lysine metabolism and its implications in human health. Its ability to improve the bioavailability of certain compounds makes it a preferred choice among formulators looking to enhance product efficacy. With its broad range of applications and benefits, Na-Methyl-L-lysine hydrochloride stands out as a key ingredient for researchers and professionals aiming to innovate in biochemistry and related fields.
Purpose
Na-Methyl-L-lysine hydrochloride is widely utilized in research focused on:
Biotechnology: It serves as a key building block in the synthesis of peptides and proteins, facilitating advancements in drug development and therapeutic applications.
Nutrition: This compound is explored for its potential benefits in dietary supplements, particularly for muscle growth and recovery, appealing to athletes and fitness enthusiasts.
Pharmaceuticals: It is used in the formulation of various medications, enhancing the efficacy of treatments for conditions like metabolic disorders.
Cosmetics: The compound is incorporated into skincare products for its moisturizing properties, providing benefits for skin health and hydration.
Research Studies: It is a valuable reagent in academic and industrial research, helping scientists understand amino acid metabolism and its implications in health and disease.
| Sonrisas canónicas | CNC(CCCCN)C(=O)O |
|---|---|
| IUPAC Name | (2S)-6-amino-2-(methylamino)hexanoic acid |
| InChIKey | OLYPWXRMOFUVGH-LURJTMIESA-N |
| INCHI | 1S/C7H16N2O2/c1-9-6(7(10)11)4-2-3-5-8/h6,9H,2-5,8H2,1H3,(H,10,11)/t6-/m0/s1 |
| Isómeros SMILES | CN[C@@H](CCCCN)C(=O)O |
| Peso molecular | 196.68 |
| Reaxy-Rn | 1723103 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723103&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| 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 Dialkylamines 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 - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Carbonyl group - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Amine - Organic oxygen compound - Organopnictogen compound - Organic oxide - 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 | N-methyl-L-alpha-amino acid - L-lysine derivative |
| Sensibilidad | light and moisture sensitive |
|---|---|
| Peso molecular | 160.210 g/mol |
| XLogP3 | -2.700 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 6 |
| Exact Mass | 160.121 Da |
| Monoisotopic Mass | 160.121 Da |
| Topological Polar Surface Area | 75.400 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 117.000 |
| 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 | 1 |
B2527657