BOC-L-Norvaline
98%
- Product Code: 144458
CAS:
53308-95-5
Molecular Weight: | 217.26 g./mol | Molecular Formula: | C₁₀H₁₉NO₄ |
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EC Number: | MDL Number: | MFCD00037268 | |
Melting Point: | 43-47 °C | Boiling Point: | 348.3 °C at 760 mmHg |
Density: | Storage Condition: | Room temperature |
Product Description:
Used in peptide synthesis as a protected amino acid building block, BOC-L-Norvaline allows for controlled assembly of peptide chains by preventing unwanted side reactions at the amino group. The BOC (tert-butoxycarbonyl) protecting group is stable under a variety of reaction conditions and can be selectively removed under mild acidic conditions, making it ideal for stepwise solid-phase or solution-phase peptide synthesis. It is particularly useful in the preparation of complex peptides and peptidomimetics for pharmaceutical research, including drug development and biochemical studies. Its structural similarity to natural amino acids helps maintain peptide conformation while enabling specific modifications to improve stability, activity, or bioavailability.
Product Specification:
Test | Specification |
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Appearance | White to Light Yellow to Beige Powder |
Purity (%) | 97.5-100 |
Specific rotation [a]20/D(C=2 in MeOH) | -16.5 Degree Celsius to -13.5 Degree Celsius |
Infrared Spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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5.000 | 10-20 days | $26.06 |
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25.000 | 10-20 days | $96.42 |
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100.000 | 10-20 days | $361.71 |
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BOC-L-Norvaline
Used in peptide synthesis as a protected amino acid building block, BOC-L-Norvaline allows for controlled assembly of peptide chains by preventing unwanted side reactions at the amino group. The BOC (tert-butoxycarbonyl) protecting group is stable under a variety of reaction conditions and can be selectively removed under mild acidic conditions, making it ideal for stepwise solid-phase or solution-phase peptide synthesis. It is particularly useful in the preparation of complex peptides and peptidomimetics for pharmaceutical research, including drug development and biochemical studies. Its structural similarity to natural amino acids helps maintain peptide conformation while enabling specific modifications to improve stability, activity, or bioavailability.
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