Fortfahren mit
A2003
Ala-Lys hydrochloride
≥98% (TLC)
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Über diesen Artikel
Empirische Formel (Hill-System):
C9H19N3O3 · HCl
CAS-Nummer:
Molekulargewicht:
253.73
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
MDL number:
Produktname
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.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Lagerklasse
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
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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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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A2003-250MG | 04061832883281 |