Z-N-Me-glu(otbu)-oh

98%

Reagent Code: #66150
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CAS Number 42417-71-0

science Other reagents with same CAS 42417-71-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.39 g/mol
Formula C₁₈H₂₅NO₆
badge Registry Numbers
MDL Number MFCD00237356
thermostat Physical Properties
Boiling Point 501 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in the construction of complex peptides, where it helps to prevent unwanted side reactions during the coupling process. The tert-butyl ester group provides stability under acidic conditions, making it suitable for use in solid-phase peptide synthesis (SPPS). Additionally, its N-methylation enhances resistance to enzymatic degradation, which is beneficial in the development of peptide-based pharmaceuticals. This chemical is also employed in the preparation of peptide libraries for drug discovery and biochemical research, enabling the exploration of new therapeutic targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,750.00

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Z-N-Me-glu(otbu)-oh
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Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in the construction of complex peptides, where it helps to prevent unwanted side reactions during the coupling process. The tert-butyl ester group provides stability under acidic conditions, making it suitable for use in solid-phase peptide synthesis (SPPS). Additionally, its N-methylation enhances resistance to enzymatic degradation, which is beneficial in the development of peptid

Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in the construction of complex peptides, where it helps to prevent unwanted side reactions during the coupling process. The tert-butyl ester group provides stability under acidic conditions, making it suitable for use in solid-phase peptide synthesis (SPPS). Additionally, its N-methylation enhances resistance to enzymatic degradation, which is beneficial in the development of peptide-based pharmaceuticals. This chemical is also employed in the preparation of peptide libraries for drug discovery and biochemical research, enabling the exploration of new therapeutic targets.

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