Boc-Asp-OH

>98%

Reagent Code: #104772
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CAS Number 13726-67-5

science Other reagents with same CAS 13726-67-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.22 g/mol
Formula C₉H₁₅NO₆
badge Registry Numbers
MDL Number MFCD00037279
thermostat Physical Properties
Melting Point 116-118 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in peptide synthesis as a protecting group for the amino group of aspartic acid, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions. The Boc group can be easily removed under acidic conditions, allowing for controlled deprotection and further modification of the peptide chain. This compound is essential in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications.

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Test Parameter Specification
Appearance White to off-white powder
Purity (%) 98-100%
Specific Rotation [α]20/D (C=1 in Methanol) -7.0
Methanol -3.0 to -7.0°
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25 g
10-20 days ฿760.00
inventory 5 g
10-20 days ฿280.00
inventory 100 g
10-20 days ฿2,850.00

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Boc-Asp-OH
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Used in peptide synthesis as a protecting group for the amino group of aspartic acid, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions. The Boc group can be easily removed under acidic conditions, allowing for controlled deprotection and further modification of the peptide chain. This compound is essential in the production of complex peptides and proteins for research, pharmaceuticals,
Used in peptide synthesis as a protecting group for the amino group of aspartic acid, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions. The Boc group can be easily removed under acidic conditions, allowing for controlled deprotection and further modification of the peptide chain. This compound is essential in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications.
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