Boc-N-Me-Aib-OH

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Reagent Code: #41169
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CAS Number 146000-39-7

science Other reagents with same CAS 146000-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD01862912
thermostat Physical Properties
Boiling Point 306.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a building block. It serves to introduce the aminoisobutyric acid (Aib) residue into peptides, which is known to stabilize peptide structures due to its unique conformational properties. The Boc (tert-butyloxycarbonyl) group acts as a protective group for the amino function, ensuring selective reactions during peptide chain assembly. This is particularly useful in the synthesis of complex peptides and peptidomimetics, where precise control over the sequence and structure is required. The N-methylation (N-Me) further enhances the peptide's resistance to enzymatic degradation, making it valuable in the development of bioactive peptides and pharmaceutical compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿13,383.00
inventory 5g
10-20 days ฿8,496.00
inventory 250mg
10-20 days ฿1,125.00
inventory 1g
10-20 days ฿2,790.00

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Boc-N-Me-Aib-OH
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This compound is primarily used in peptide synthesis as a building block. It serves to introduce the aminoisobutyric acid (Aib) residue into peptides, which is known to stabilize peptide structures due to its unique conformational properties. The Boc (tert-butyloxycarbonyl) group acts as a protective group for the amino function, ensuring selective reactions during peptide chain assembly. This is particularly useful in the synthesis of complex peptides and peptidomimetics, where precise control over the

This compound is primarily used in peptide synthesis as a building block. It serves to introduce the aminoisobutyric acid (Aib) residue into peptides, which is known to stabilize peptide structures due to its unique conformational properties. The Boc (tert-butyloxycarbonyl) group acts as a protective group for the amino function, ensuring selective reactions during peptide chain assembly. This is particularly useful in the synthesis of complex peptides and peptidomimetics, where precise control over the sequence and structure is required. The N-methylation (N-Me) further enhances the peptide's resistance to enzymatic degradation, making it valuable in the development of bioactive peptides and pharmaceutical compounds.

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