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W384720

Sigma-Aldrich

L-Lysine

≥98%, FG

Synonym(s):

(S)-2,6-Diaminocaproic acid

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About This Item

Linear Formula:
H2N(CH2)4CH(NH2)CO2H
CAS Number:
Molecular Weight:
146.19
FEMA Number:
3847
Beilstein/REAXYS Number:
1722531
EC Number:
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
17.026

biological source

synthetic

Quality Level

grade

FG
Halal
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.320

assay

≥98%

mp

215 °C (dec.) (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

odorless

SMILES string

NCCCC[C@H](N)C(O)=O

InChI

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

InChI key

KDXKERNSBIXSRK-YFKPBYRVSA-N

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Related Categories

Application


  • Novel recombinant aminoacylase from Paraburkholderia monticola capable of N-acyl-amino acid synthesis: Discusses a new enzyme capable of utilizing L-Lysine for synthesizing N-acyl-amino acids, paving the way for advancements in biochemical syntheses and industrial applications (Haeger et al., 2024).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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L-Lysine monohydrate for biochemistry

Millipore

1.12233

L-Lysine monohydrate

L-Lysine monohydrochloride certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

67448

L-Lysine monohydrochloride

Giacomo Damilano et al.
Organic & biomolecular chemistry, 17(45), 9778-9791 (2019-11-09)
This study investigates the synthesis of β-branched amines and β-branched quaternary ammonium chloride ionic liquids as novel extractants. The synthesis methodology was tailored to facilitate the reaction scale-up and the use of biorenewable starting materials. The developed process is an

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