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Key Documents

282677

Sigma-Aldrich

L-Lysine hydrate

97%

Synonym(s):

(S)-(+)-Lysine

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About This Item

Linear Formula:
H2N(CH2)4CH(NH2)CO2H · xH2O
CAS Number:
Molecular Weight:
146.19 (anhydrous basis)
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

optical activity

[α]21/D +22°, c = 2 in 6 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

SMILES string

OC([C@@H](N)CCCCN)=O.O

InChI

1S/C6H14N2O2.H2O/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H2/t5-;/m0./s1

InChI key

HZRUTVAFDWTKGD-JEDNCBNOSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Dong Hoon Han et al.
Nature communications, 5, 5633-5633 (2014-12-06)
The 26S proteasome is the primary machinery that degrades ubiquitin (Ub)-conjugated proteins, including many proteotoxic proteins implicated in neurodegeneraton. It has been suggested that the elevation of proteasomal activity is tolerable to cells and may be beneficial to prevent the

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