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Nε,Nε,Nε-Trimethyllysine hydrochloride - ≥97% (TLC), high purity , CAS No.55528-53-5
a non-protein amino acid active in the biosynthesis of carnitine
Basic Description
Synonyms
1-Pentanaminium | 5-amino-5-carboxy-N,N,N-trimethyl-, chloride (1:1) | H-Nε-(trimethyl)-L-lysine chloride
Specifications & Purity
≥97%(TLC)
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Nε-trimethyllysine (TML) is a non-protein amino acid which takes part in the biosynthesis of carnitine. In mammals, the breakdown of endogenous proteins containing TML residues is a starting point for carnitine biosynthesis. Nε,Nε,Nε-Trimethyllysine hydrochloride is primarly used in lysine methylation modification assays and purifications.
Taxonomic Classification
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 Tetraalkylammonium salts Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic oxides Organic chloride salts Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
L-alpha-amino acid - Medium-chain fatty acid - Fatty acid - Fatty acyl - Quaternary ammonium salt - Tetraalkylammonium salt - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Organic salt - Organic zwitterion - Organic oxygen compound - Organic nitrogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Carbonyl group - Hydrocarbon derivative - Organic chloride salt - 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
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.
Names and Identifiers
IUPAC Name
[(5S)-5-amino-5-carboxypentyl]-trimethylazanium;chloride
INCHI
InChI=1S/C9H20N2O2.ClH/c1-11(2,3)7-5-4-6-8(10)9(12)13;/h8H,4-7,10H2,1-3H3;1H/t8-;/m0./s1
InChIKey
ZKIJKCHCMFGMCM-QRPNPIFTSA-N
Smiles
C[N+](C)(C)CCCCC(C(=O)O)N.[Cl-]
Isomeric SMILES
C[N+](C)(C)CCCC[C@@H](C(=O)O)N.[Cl-]
Molecular Weight
224.73
Reaxy-Rn
6304303
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6304303&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in Water
Molecular Weight
224.730 g/mol
XLogP3
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
6
Exact Mass
224.129 Da
Monoisotopic Mass
224.129 Da
Topological Polar Surface Area
63.300 Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
163.000
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
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F2520461