BOC-L-GLUTAMINE 4-NITROPHENYL ESTER
≥95%
Reagent
Code: #104805
Alias
4-Nitrophenyl(S)-5-amino-2-((tert-butoxycarbonyl)amino)-5-oxopentanoate; 2-tert-butoxycarbonylamino-4-carbamoylbutanoic acid 4 -Nitrophenyl ester;Boc-Gln-ONp;4-nitrophenyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-carbamoylbutanoate
CAS Number
15387-45-8
blur_circular Chemical Specifications
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Molecular Information
Weight
367.35 g/mol
Formula
C₁₆H₂₁N₃O₇
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Registry Numbers
MDL Number
MFCD00065572
thermostat
Physical Properties
Boiling Point
617.5±55.0 °C at 760 mmHg
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Storage & Handling
Density
1.291±0.06 g/cm3
Storage
2-8°C, dry, sealed
description Product Description
BOC-L-Glutamine 4-nitrophenyl ester is primarily used in peptide synthesis as a protected amino acid derivative. The BOC (tert-butoxycarbonyl) group serves as a protective group for the amine functionality, preventing unwanted reactions during the synthesis process. The 4-nitrophenyl ester moiety is highly reactive, making it an effective acylating agent for coupling with other amino acids or peptides. This compound is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase peptide synthesis, where it facilitates the formation of peptide bonds with high efficiency. Its application is critical in the production of complex peptides and proteins for research in biochemistry, pharmaceuticals, and biotechnology. Additionally, it is employed in the study of enzyme mechanisms and protein interactions due to its ability to introduce specific amino acid sequences into peptides.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| APPEARANCE | White to Off-white Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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