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Supelco

L-Lysine hydrochloride solution

100 mM amino acid in 0.1 M HCl, analytical standard

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About This Item

Formula empirica (notazione di Hill):
C6H14N2O2 · HCl
Numero CAS:
Peso molecolare:
182.65
Beilstein:
5460909
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Forma fisica

liquid

Classi chimiche degli analiti

amino acids, peptides, proteins

Concentrazione

100 mM amino acid in 0.1 M HCl

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Colore

colorless

applicazioni

food and beverages

Formato

single component solution

Temperatura di conservazione

2-8°C

Stringa SMILE

Cl.NCCCC[C@H](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/t5-;/m0./s1
BVHLGVCQOALMSV-JEDNCBNOSA-N

Descrizione generale

L-Lysine hydrochloride is one of the essential amino acids which usually finds applications in the treatment of shingles and genital as well mouth lesions attributed to herpes zoster and herpes simplex virus, respectively.

Applicazioni

L-Lysine hydrochloride may be used as a reference standard for the determination of L-lysine hydrochloride in pharmaceutical dosage form by high resolution high performance liquid chromatography (HR-HPLC). It may be used as a precursor of lysine for its determination in breath condensate by isotope dilution hydrophilic-interaction liquid chromatography combined with tandem mass spectrometry (HILIC-MS/MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

Corrosion

Avvertenze

Warning

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Met. Corr. 1

Codice della classe di stoccaggio

8B - Non-combustible, corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

nwg

Dispositivi di protezione individuale

Eyeshields, Gloves


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Indian Journal of Pharmaceutical Sciences, 77(4), 434-434 (2015)
Simultaneous determination of the advanced glycation end product Nε-carboxymethyllysine and its precursor, lysine, in exhaled breath condensate using isotope-dilution-hydrophilic-interaction liquid chromatography coupled to tandem mass spectrometry
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The aim of this study was to develop by means of co-extrusion a multilayer fixed-dose combination solid dosage form for oral application characterized by immediate release for both layers, the layers containing different drugs with different water-solubility. In this study

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