H-ASP(OET)-OET HCL
98%
- Product Code: 105284
Alias:
L-Aspartic Acid Diethyl Ester Hydrochloride L-Aspartic Acid Diethyl Ester
CAS:
16115-68-7
| Molecular Weight: | 225.67 g./mol | Molecular Formula: | C₈H₁₆ClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038910 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
This compound is primarily used in peptide synthesis as a protected form of aspartic acid. The ethoxy groups act as protecting groups for the carboxylic acid functionality, preventing unwanted reactions during peptide bond formation. It is particularly useful in solid-phase peptide synthesis (SPPS) where selective deprotection and coupling steps are required. The hydrochloride salt form enhances its stability and solubility in various solvents, making it easier to handle in laboratory settings. Additionally, it finds application in the development of peptide-based pharmaceuticals and biochemical research, where precise control over amino acid incorporation is essential. Its use ensures high yield and purity in the synthesis of complex peptides.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 98-100 |
| Appearance | White To Almost White Powder To Crystal To Crystalline Powder |
| Melting Point | 105-109 |
| Specific Rotation [a]20/D(C=1, H2O) | 7.0-+9.0 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿450.00 |
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| 25.000 | 10-20 days | ฿1,220.00 |
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| 100.000 | 10-20 days | ฿4,600.00 |
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| 500.000 | 10-20 days | ฿20,600.00 |
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H-ASP(OET)-OET HCL
This compound is primarily used in peptide synthesis as a protected form of aspartic acid. The ethoxy groups act as protecting groups for the carboxylic acid functionality, preventing unwanted reactions during peptide bond formation. It is particularly useful in solid-phase peptide synthesis (SPPS) where selective deprotection and coupling steps are required. The hydrochloride salt form enhances its stability and solubility in various solvents, making it easier to handle in laboratory settings. Additionally, it finds application in the development of peptide-based pharmaceuticals and biochemical research, where precise control over amino acid incorporation is essential. Its use ensures high yield and purity in the synthesis of complex peptides.
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