L0645
L-Lysine methyl ester dihydrochloride
≥99% (TLC)
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About This Item
Empirical Formula (Hill Notation):
C7H16N2O2 · 2HCl
CAS Number:
Molecular Weight:
233.14
EC Number:
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
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product name
L-Lysine methyl ester dihydrochloride,
Assay
≥99% (TLC)
form
powder
color
white
storage temp.
−20°C
SMILES string
Cl.COC(=O)C(N)CCCCN
InChI
1S/C7H16N2O2.ClH/c1-11-7(10)6(9)4-2-3-5-8;/h6H,2-5,8-9H2,1H3;1H
InChI key
FORVAIDSGSLRPX-UHFFFAOYSA-N
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Application
L-Lysine methyl ester is used in the production of lysine methyl ester based cationic surfactants and hydrogels.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Langmuir : the ACS journal of surfaces and colloids, 25(14), 7803-7814 (2009-07-15)
The synthesis of a novel class of lysine-based cationic amphiphilic derivatives of the type N(epsilon),N(epsilon)'-bis(n-acyloxypropyl)-l-lysine methyl ester salts combining several hydroxyl functions and aliphatic chains of 12 or 14 carbon atoms is described. The compounds have one, two, three, and
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C O Mills et al.
Biochimica et biophysica acta, 1336(3), 485-496 (1997-11-21)
We have synthesised and characterised a fluorescent monohydroxy bile salt analogue, lithocholyl-lysyl-fluorescein and compared its physical and biological properties with those of lithocholate, glycolithocholate, sulpholithocholate, lithocholic acid glucuronide and taurocholate. The synthetic method used excess N-epsilon-CBZ-L-lysine methyl ester hydrochloride and
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Dynamic light scattering (DLS) and rheological experiments have been performed on semidilute aqueous hyaluronic acid (HA) solutions during the chemical cross-linking process with a water-soluble carbodiimide (WSC) to produce a hydrogel. The formation and destruction of the gel are characterized.
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