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A2003

Sigma-Aldrich

Ala-Lys hydrochloride

≥98% (TLC)

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About This Item

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

product name

Ala-Lys hydrochloride,

Ensaio

≥98% (TLC)

forma

powder

cor

white to off-white

aplicação(ões)

peptide synthesis

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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

chave InChI

JWNUXAHYKKBLRA-UHFFFAOYSA-N

Ações bioquímicas/fisiológicas

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.

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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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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
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
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

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