62840
L-Lysine
≥98.0% (NT), for peptide synthesis
동의어(들):
(S)-2,6-Diaminocaproic acid
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
H2N(CH2)4CH(NH2)CO2H
CAS 번호:
Molecular Weight:
146.19
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
200-294-2
MDL number:
Beilstein/REAXYS Number:
1722531
제품 이름
L-Lysine, crystallized, ≥98.0% (NT)
SMILES string
NCCCC[C@H](N)C(O)=O
InChI key
KDXKERNSBIXSRK-YFKPBYRVSA-N
InChI
1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10)/t5-/m0/s1
assay
≥98.0% (NT)
form
solid
optical activity
[α]20/D +26.0±1.0°, c = 2% in 6 M HCl
quality
crystallized
reaction suitability
reaction type: solution phase peptide synthesis
impurities
≤1% water
mp
215 °C (dec.) (lit.), ~215 °C (dec.)
solubility
H2O: 0.1 g/mL, clear, colorless to very faintly greenish-yellow
application(s)
peptide synthesis
Quality Level
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General description
L-lysine is an amino acid commonly used as a building block in solid-phase peptide synthesis (SSPS).
Application
L-lysine serves as a precursor in the formation of polymeric structures.It is also used for the synthesis and modification of chitosan resin.
저장 등급
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Adsorption of platinum (IV), palladium (II) and gold (III) from aqueous solutions onto l-lysine modified crosslinked chitosan resin
K Fujiwara et al.
Journal of Hazardous Materials, 146, 39-50 (2007)
Hierarchical nanofabrication of microporous crystals with ordered mesoporosity.
Fan W
Nature Materials, 7(12), 984-984 (2008)
Fluorescent labeling of peptides on solid phase
AR Katritzky, et al.
Organic & Biomolecular Chemistry, 6, 4582-4586 (2008)
Modulating the poly-l-lysine structure through the control of the protonation--deprotonation state of l-lysine
L Stagi, et al.
Scientific Reports, 12, 19719-19719 (2022)
Sofia Faraasen et al.
Pharmaceutical research, 20(2), 237-246 (2003-03-15)
The purpose of this study was to demonstrate specific receptor-mediated targeting of phagocytes by functional surface coatings of microparticles, shielding from nonspecific phagocytosis and allowing ligand-specific interactions via molecular recognition. Coatings of the comb polymer poly(L-lysine)-g-poly(ethylene glycol) (PLL-g-PEG) were investigated
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