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L6001

Sigma-Aldrich

DL-Lysine monohydrochloride

≥98% (HPLC)

Sinônimo(s):

DL-2,6-Diaminohexanoic acid monohydrochloride

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About This Item

Fórmula linear:
NH2(CH2)4CH(NH2)COOH · HCl
Número CAS:
70-53-1
Peso molecular:
182.65
Beilstein:
4711993
Número CE:
200-739-0
Número MDL:
MFCD00064563
Código UNSPSC:
12352209
ID de substância PubChem:
24896425
NACRES:
NA.26

product name

DL-Lysine monohydrochloride, ≥98% (HPLC)

Ensaio

≥98% (HPLC)

forma

powder

cor

white to off-white

pf

267 °C (dec.) (lit.)

solubilidade

H2O: soluble

aplicação(ões)

peptide synthesis

cadeia de caracteres SMILES

Cl.NCCCCC(N)C(O)=O

InChI

1S/C6H14N2O2.ClH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H

chave InChI

BVHLGVCQOALMSV-UHFFFAOYSA-N

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Categorias relacionadas

Ações bioquímicas/fisiológicas

DL-Lysine monohydrochloride is a racemic mixture of the D- and L- enantiomers of lysine. DL-Lysine may be used to construct polylysine polymers useful to produce lysine-based polypeptide gels and films.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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D-Ornithine monohydrochloride ~98%

Sigma-Aldrich

O5250

D-Ornithine monohydrochloride

L-Lysine hydrochloride solution 100 mM amino acid in 0.1 M HCl, analytical standard

Supelco

44208

L-Lysine hydrochloride solution

Mamoru K Kokufuta et al.
Colloids and surfaces. B, Biointerfaces, 87(2), 299-309 (2011-06-21)
We synthesized the glutaraldehyde cross-linked hydrogels using four kinds of poly(lysine)s (PLs) and measured the equilibrium swelling ratio (Q) as a function of pH. Also measured was the temperature change of Q at a fixed pH (11.6) in the absence
K Itoh et al.
Langmuir : the ACS journal of surfaces and colloids, 24(23), 13426-13433 (2008-11-01)
The buildup mechanism of polypeptide multilayers prepared by the layer-by-layer deposition of a polyanion (poly(L-glutamic acid) (PGA)) and polycations (poly(L-lysine) (PLL), poly(D-lysine) (PDL), and copoly(DL-lysine)(PDLL)) was reinvestigated by using in situ ATR-IR spectroscopy. A difference spectral technique applied to analyze
Pasquale De Santis et al.
Journal of nanoscience and nanotechnology, 7(7), 2230-2238 (2007-08-01)
Organic trans-annular assemblies constitute an expanding class of structures with promising applications for the design of nanotechnological devices. Among the strategies developed for the engineering of organic nanotubes, those characterized by regular alternating enantiomeric amino acid sequences have been proven
Preparation of hierarchical mesocrystalline DL-lysine·HCl-poly(acrylic acid) hybrid thin films.
Yuan Jiang et al.
Advanced materials (Deerfield Beach, Fla.), 23(31), 3548-3552 (2011-07-05)
Moyu Taniguchi et al.
Journal of bioscience and bioengineering, 124(4), 414-418 (2017-06-02)
Although naturally abundant amino acids are represented mainly by l-enantiomers, fermented foods are known to contain various d-amino acids. Enantiospecific profiles of food products can vary due to fermentation by bacteria, and such alterations may contribute to changes in food
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