L-Aspartic acid di-tert-butyl ester hydrochloride
99%
- Product Code: 97531
Alias:
L-Aspartic Acid Di-tert-Butyl Ester Hydrochloride
CAS:
1791-13-5
Molecular Weight: | 281.78 g./mol | Molecular Formula: | C₁₂H₂₃NO₄HCl |
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EC Number: | MDL Number: | MFCD00034851 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
L-Aspartic acid di-tert-butyl ester hydrochloride is primarily used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. This compound helps prevent unwanted side reactions during the formation of peptide bonds, ensuring higher purity and yield of the final peptide product. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required. Additionally, it finds application in the synthesis of complex organic molecules and pharmaceuticals, where precise control over reactivity is essential. Its stability under various reaction conditions makes it a reliable choice in organic and medicinal chemistry research.
Product Specification:
Test | Specification |
---|---|
PURITYHPLC | 99 100% |
MELTING POINT | 130-150 |
ETHANOL | 8-12 |
APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿840.00 |
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25.000 | 10-20 days | ฿2,960.00 |
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100.000 | 10-20 days | ฿9,790.00 |
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L-Aspartic acid di-tert-butyl ester hydrochloride
L-Aspartic acid di-tert-butyl ester hydrochloride is primarily used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. This compound helps prevent unwanted side reactions during the formation of peptide bonds, ensuring higher purity and yield of the final peptide product. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection is required. Additionally, it finds application in the synthesis of complex organic molecules and pharmaceuticals, where precise control over reactivity is essential. Its stability under various reaction conditions makes it a reliable choice in organic and medicinal chemistry research.
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