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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Nα,Nα-Bis(carboxymethyl)-L-lysine hydrate

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Chemical Name: Nα,Nα-Bis(carboxymethyl)-L-lysine hydrate
CAS Number: 941689-36-7
Product Number: AG00H1US(AGN-PC-0WAJNQ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
280.277g/mol
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
10
Exact Mass:
280.127g/mol
Monoisotopic Mass:
280.127g/mol
Topological Polar Surface Area:
142A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
291
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N2,N2-bis(carboxymethyl)-L-Lysine hydrate, also known as lysine bis-MPA, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of collagen-like peptides, which are important for various applications in the fields of biomedicine and materials science. In chemical synthesis, N2,N2-bis(carboxymethyl)-L-Lysine hydrate is crucial for its ability to function as a strong metal chelator, forming stable complexes with metal ions. This property makes it a valuable tool in the development of metal-based catalysts and metalloprotein mimetics. Additionally, the presence of carboxymethyl groups enhances the solubility of the compound in aqueous solutions, facilitating its use in a wide range of biological and chemical reactions.