H-Lys(Boc)-OMe hydrochloride

98%

  • Product Code: 105415
  Alias:    N(e)-tert-butoxycarbonyl-L-lysine methyl ester hydrochloride
  CAS:    2389-48-2
Molecular Weight: 296.79 g./mol Molecular Formula: C₁₂H₂₄N₂O₄HCl
EC Number: MDL Number: MFCD00076959
Melting Point: Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used extensively in peptide synthesis as a protected form of lysine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group during the synthesis process, preventing unwanted reactions. After the peptide chain is assembled, the Boc group can be selectively removed under acidic conditions, exposing the amino group for further modifications or coupling reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and in the production of complex peptides for pharmaceutical research, including the development of therapeutic peptides and peptide-based drugs. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry.
Product Specification:
Test Specification
Melting Point 155
Purity (HPLC) 98-100
Specific Rotation [A]20/D(C=1 In Meoh) 14-18
Appearance White To Off-White Powder Or Crystals
Proton NMR Spectrum Conforms To Structure
TLC Analysis One Spot
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿620.00
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-
5.000 10-20 days ฿2,290.00
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-
H-Lys(Boc)-OMe hydrochloride
Used extensively in peptide synthesis as a protected form of lysine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group during the synthesis process, preventing unwanted reactions. After the peptide chain is assembled, the Boc group can be selectively removed under acidic conditions, exposing the amino group for further modifications or coupling reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and in the production of complex peptides for pharmaceutical research, including the development of therapeutic peptides and peptide-based drugs. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry.
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