Boc-Asp(OtBu)-OH

95%

Reagent Code: #105727
label
Alias tert-Butoxycarbonyl-L-Aspartic Acid-4-tert-Butyl Ester ; BOC-L-Aspartic Acid-4-tert-Butyl Ester
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CAS Number 1676-90-0

science Other reagents with same CAS 1676-90-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.32 g/mol
Formula C₁₃H₂₃NO₆
badge Registry Numbers
MDL Number MFCD00076912
thermostat Physical Properties
Melting Point 64-67 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in peptide synthesis as a building block. It serves as a protected form of aspartic acid, ensuring specific reactions occur at desired sites without interference. The Boc (tert-butyloxycarbonyl) and OtBu (tert-butyl ester) groups protect the amino and carboxyl functionalities, respectively, during the synthesis process. This allows for controlled step-by-step assembly of peptide chains. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling are essential. Its application ensures high purity and efficiency in producing complex peptides for research, pharmaceuticals, and biotechnology.

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Test Parameter Specification
Melting Point 60-65
Purity (HPLC) 94.5-100
Specific Rotation [a]20/d (c = 1% In Methanol)
Specific Rotation [α]20/D (c = 1% in Methanol) 1.6-2.4
TLC Analysis One Spot
Appearance White To Off-White Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿630.00
inventory 25g
10-20 days ฿2,850.00
inventory 100g
10-20 days ฿11,280.00

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Boc-Asp(OtBu)-OH
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This chemical is widely used in peptide synthesis as a building block. It serves as a protected form of aspartic acid, ensuring specific reactions occur at desired sites without interference. The Boc (tert-butyloxycarbonyl) and OtBu (tert-butyl ester) groups protect the amino and carboxyl functionalities, respectively, during the synthesis process. This allows for controlled step-by-step assembly of peptide chains. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling are essential. Its application ensures high purity and efficiency in producing complex peptides for research, pharmaceuticals, and biotechnology.
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