N-Carbobenzyloxy-L-leucine
90%
Reagent
Code: #105552
Alias
N-Benzyloxycarbonyl-L-leucine; N-carboxy-L-leucine, CBZ-L-leucine
CAS Number
2018-66-8
blur_circular Chemical Specifications
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Molecular Information
Weight
265.3 g/mol
Formula
C₁₄H₁₉NO₄
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Registry Numbers
EC Number
217-960-3
MDL Number
MFCD00026494
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Storage & Handling
Density
1 g/mL at 25 °C(lit.)
Storage
2-8°C
description Product Description
N-Carbobenzyloxy-L-leucine is primarily used in peptide synthesis as a protecting group for the amino group of leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds accurately. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of amino acids are crucial. Additionally, it finds applications in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where precise control over molecular structure is essential for efficacy and safety. Its role in organic synthesis also extends to the preparation of intermediates for various bioactive compounds.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to pale yellow viscous liquid |
Purity (%) | 89.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
shopping_cart Available Sizes & Pricing
N-Carbobenzyloxy-L-leucine
N-Carbobenzyloxy-L-leucine is primarily used in peptide synthesis as a protecting group for the amino group of leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds accurately. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of amino acids are crucial. Additionally, it finds applications in the development of pharmaceuticals, especially in the creation of peptide-based drugs, where precise control over molecular structure is essential for efficacy and safety. Its role in organic synthesis also extends to the preparation of intermediates for various bioactive compounds.
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