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D-LYSINE METHYL ESTER DIHYDROCHLORIDE

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CAS:67396-08-1
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CAS:67396-08-1
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D-LYSINE METHYL ESTER DIHYDROCHLORIDE manufacturers

  • D-Lys-Ome.2Hcl
  • D-Lys-Ome.2Hcl pictures
  • $0.00 / 1kg
  • 2025-11-03
  • CAS:67396-08-1
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
D-LYSINE METHYL ESTER DIHYDROCHLORIDE Basic information
Product Name:D-LYSINE METHYL ESTER DIHYDROCHLORIDE
Synonyms:D-Lys-OMe 2HCl;methyl (2R)-2,6-diaminohexanoate dihydrochloride;D-Lysine Methyl Ester Dihydrochloride;METHYL 2,6-DIAMINOHEXANOATE DIHYDROCHLORIDE;(R)-Methyl 2,6-diaminohexanoate dihydrochloride;D-LysineMethylEsterDihydrochloride>;D-LYSINE METHYL ESTER DIHYDROCHLORIDE USP/EP/BP;(R)-Methyl 2,6-diaminohexanoate
CAS:67396-08-1
MF:C7H16N2O2.2HCl
MW:0
EINECS:
Product Categories:Amino Acid Methyl Esters;Amino Acids;Amino Acids (C-Protected);Biochemistry
Mol File:67396-08-1.mol
D-LYSINE METHYL ESTER DIHYDROCHLORIDE Structure
D-LYSINE METHYL ESTER DIHYDROCHLORIDE Chemical Properties
Melting point 205 °C
refractive index -17 ° (C=5, H2O)
storage temp. Inert atmosphere,Room Temperature
Water Solubility Soluble in water
solubility Methanol (Slightly), Water (Slightly)
form powder to crystal
color White to Almost white
Stability:Hygroscopic
CAS DataBase Reference67396-08-1
Safety Information
HS Code 2922.41.0090
MSDS Information
D-LYSINE METHYL ESTER DIHYDROCHLORIDE Usage And Synthesis
UsesD-Lysine Methyl Ester is a protected form of D-Lysine (L468930). D-Lysine is the unnatural isomer of L-Lysine (L468895) that has the ability to reduce non-enzymatic glycation in vitro. D-Lysine also exists as polypeptide chains of poly-D-lysine, a nonspecific adhesion-promoting molecule that has the potential to be a polymeric drug carrier.
Synthesis
Methanol

67-56-1

L-Lysine hydrochloride

657-27-2

methyl 2,6-diaminohexanoate hydrochloride

13515-95-2

L-lysine hydrochloride (2, 5.00 g, 27.4 mmol, 1.0 eq.) and methanol (30 mL, 0.9 M) were added to a round bottom flask. The suspension was heated to reflux to completely dissolve the solid. Thionyl chloride (2.59 mL, 35.6 mmol, 1.3 eq.) was added slowly and dropwise over 15 min. The reaction mixture was kept under reflux conditions for 17 hours. Removal of most of the volatiles (~25 mL) by distillation followed by azeotropic removal of the remaining volatiles by toluene under reduced pressure afforded pure lysine methyl ester dihydrochloride (3, quantitative mass recovery, white solid), which was used directly in the next step of the reaction without further purification. The product was analyzed and the data were consistent with those reported in the literature.

References[1] Tetrahedron Letters, 2016, vol. 57, # 4, p. 502 - 504
[2] Journal of Medicinal Chemistry, 2002, vol. 45, # 17, p. 3669 - 3683
[3] Heterocycles, 2017, vol. 94, # 5, p. 964 - 978
[4] Journal of Polymer Science, Part A: Polymer Chemistry, 2015, vol. 53, # 17, p. 2036 - 2049
[5] Molecules, 2016, vol. 21, # 1,
D-LYSINE METHYL ESTER DIHYDROCHLORIDE Preparation Products And Raw materials
Raw materialsMethanol-->L-Lysine hydrochloride-->L-Lysine-->2,2-Dimethoxypropane
Tag:D-LYSINE METHYL ESTER DIHYDROCHLORIDE(67396-08-1) Related Product Information
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