Z-Asp(OMe)-OH
98.0%
- Product Code: 105663
CAS:
3160-47-2
| Molecular Weight: | 281.26 g./mol | Molecular Formula: | C₁₃H₁₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00133585 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Z-Asp(OMe)-OH is widely used in peptide synthesis as a protected form of aspartic acid. Its primary application is in the construction of peptides where aspartic acid needs to be incorporated without unwanted side reactions. The methoxy (OMe) group protects the carboxylic acid functionality, ensuring selective reactions at other sites during peptide chain elongation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where protecting groups are essential for controlling the sequence and integrity of the peptide. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise amino acid incorporation is critical for maintaining the desired biological activity. Its stability and ease of deprotection make it a reliable choice for researchers and industrial applications in peptide chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,548.00 |
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| 25.000 | 10-20 days | ฿5,724.00 |
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Z-Asp(OMe)-OH
Z-Asp(OMe)-OH is widely used in peptide synthesis as a protected form of aspartic acid. Its primary application is in the construction of peptides where aspartic acid needs to be incorporated without unwanted side reactions. The methoxy (OMe) group protects the carboxylic acid functionality, ensuring selective reactions at other sites during peptide chain elongation. This compound is particularly valuable in solid-phase peptide synthesis (SPPS) and solution-phase methods, where protecting groups are essential for controlling the sequence and integrity of the peptide. Additionally, it is utilized in the development of pharmaceuticals and bioactive peptides, where precise amino acid incorporation is critical for maintaining the desired biological activity. Its stability and ease of deprotection make it a reliable choice for researchers and industrial applications in peptide chemistry.
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