N-Me-D-His-OMe·HCl

97%

Reagent Code: #219426
fingerprint
CAS Number 1219090-51-3

science Other reagents with same CAS 1219090-51-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.671 g/mol
Formula C₈H₁₄ClN₃O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in peptide synthesis as a protected histidine derivative, particularly in the development of bioactive peptides where methylation and esterification help modulate stability and receptor selectivity. The hydrochloride salt form improves solubility and handling in aqueous-based reactions. Commonly employed in pharmaceutical research for designing enzyme inhibitors or hormone analogs due to enhanced metabolic resistance provided by the N-methyl and methyl ester modifications. Also utilized in solid-phase peptide synthesis (SPPS) to prevent side reactions at the imidazole ring during coupling steps.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,990.00
N-Me-D-His-OMe·HCl
No image available

Used in peptide synthesis as a protected histidine derivative, particularly in the development of bioactive peptides where methylation and esterification help modulate stability and receptor selectivity. The hydrochloride salt form improves solubility and handling in aqueous-based reactions. Commonly employed in pharmaceutical research for designing enzyme inhibitors or hormone analogs due to enhanced metabolic resistance provided by the N-methyl and methyl ester modifications. Also utilized in solid-pha

Used in peptide synthesis as a protected histidine derivative, particularly in the development of bioactive peptides where methylation and esterification help modulate stability and receptor selectivity. The hydrochloride salt form improves solubility and handling in aqueous-based reactions. Commonly employed in pharmaceutical research for designing enzyme inhibitors or hormone analogs due to enhanced metabolic resistance provided by the N-methyl and methyl ester modifications. Also utilized in solid-phase peptide synthesis (SPPS) to prevent side reactions at the imidazole ring during coupling steps.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...