Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

282677

Sigma-Aldrich

L-Lysine hydrate

97%

Synonym(s):

(S)-(+)-Lysine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
H2N(CH2)4CH(NH2)CO2H · xH2O
CAS Number:
199926-21-1
Molecular Weight:
146.19 (anhydrous basis)
MDL number:
MFCD00151035
UNSPSC Code:
12352209
PubChem Substance ID:
24857062
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 Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK7853
STBK3651
STBJ8352
STBJ8326
STBJ0931

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service