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About This Item
Empirical Formula (Hill Notation):
C7H16N2O2 · 2HCl
CAS Number:
Molecular Weight:
233.14
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
247-625-7
MDL number:
Pricing and availability is not currently available.
Product Name
L-Lysine methyl ester dihydrochloride,
assay
≥99% (TLC)
Quality Level
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
Application
L-Lysine methyl ester is used in the production of lysine methyl ester based cationic surfactants and hydrogels.
1 of 1
This Item | |||
|---|---|---|---|
| form powder | form powder | form powder | form powder |
| assay ≥99% (TLC) | assay ≥98% (TLC) | assay ≥98% (TLC) | assay ≥99% (TLC) |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| color white | color white | color white | color white |
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Aurora Pinazo et al.
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
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
Atoosa Maleki et al.
Carbohydrate research, 342(18), 2776-2792 (2007-09-29)
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.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| L0645-25G | 04061832416748 |
| L0645-5G | 04061833948903 |



