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A2003

Sigma-Aldrich

Ala-Lys hydrochloride

≥98% (TLC)

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About This Item

Fórmula empírica (notación de Hill):
C9H19N3O3 · HCl
Número de CAS:
68973-27-3
Peso molecular:
253.73
MDL number:
MFCD00058293
UNSPSC Code:
12352202
PubChem Substance ID:
24890611
NACRES:
NA.26

Nombre del producto

Ala-Lys hydrochloride,

assay

≥98% (TLC)

form

powder

color

white to off-white

application(s)

peptide synthesis

storage temp.

−20°C

SMILES string

Cl.CC(N)C(=O)NC(CCCCN)C(O)=O

InChI

1S/C9H19N3O3.ClH/c1-6(11)8(13)12-7(9(14)15)4-2-3-5-10;/h6-7H,2-5,10-11H2,1H3,(H,12,13)(H,14,15);1H

InChI key

JWNUXAHYKKBLRA-UHFFFAOYSA-N

Biochem/physiol Actions

Alanyl dipeptides such as ala-leu, ala-lys, ala-gly, ala-pro, ala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análisis (COA)

Lot/Batch Number
BCCD5339
BCBR7234V
BCBL0178V
BCBD6914V
1398673

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Víctor Cruz et al.
The journal of physical chemistry. B, 115(16), 4880-4886 (2011-04-08)
An exhaustive umbrella sampling simulation of the alanine dipeptide in solution is reported. The presence of stable Y conformations in solution is assessed by both quantum calculations and experimental data from X-ray and NMR protein-solved structures available in the protein
Voislav Blagojevic et al.
Analytical chemistry, 83(9), 3470-3476 (2011-04-21)
The ability to resolve isomeric protonated dipeptides was investigated with the new technique of differential ion mobility mass spectrometry that uses "modifier" molecules to enhance differential mobility. Two pairs of protonated peptides [glycine-alanine (GlyAla) and alanine-glycine (AlaGly), glycine-serine (GlySer) and
Marie-Pierre Gaigeot
Physical chemistry chemical physics : PCCP, 12(35), 10198-10209 (2010-06-12)
Following our previous work [J. Phys. Chem. B. Lett., 2009, 113, 10059], DFT-based molecular dynamics (DFTMD) simulations of 2-Ala peptide (i.e. Ac-Ala-NHMe dialanine peptide analog with methyl group caps at the extremities) immersed in liquid water at room temperature are
Trang U Vo et al.
Electrophoresis, 25(9), 1230-1236 (2004-06-03)
Series of dipeptides, including homodipeptides and alanyl dipeptides, were separated using quadruplex (G-quartet) DNA stationary phases in open-tubular capillary electrochromatography (OTCEC). The stationary phases were constructed by covalently attaching the DNA oligonucleotides to the inner capillary surface. Three different G-quartet

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