L-Alanine benzyl ester hydrochloride
98%
- Product Code: 76438
Alias:
Alanine-alpha-benzyl ester hydrochloride L-alanine benzyl ester hydrochloride Alanine-alpha-benzyl ester hydrochloride L-alanine benzyl ester p-hydrochloride
CAS:
5557-83-5
| Molecular Weight: | 215.68 g./mol | Molecular Formula: | C₁₀H₁₄ClNO₂ |
|---|---|---|---|
| EC Number: | 226-920-4 | MDL Number: | MFCD00054340 |
| Melting Point: | 135-145 ℃ | Boiling Point: | 293ºC at 760 mmHg |
| Density: | 1.1 g/cm3 | Storage Condition: | -20°C |
Product Description:
L-Alanine benzyl ester hydrochloride is primarily used in the synthesis of peptides and other organic compounds. It serves as a protected form of alanine, where the benzyl ester group safeguards the carboxyl functionality during chemical reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Additionally, it is employed in the preparation of amino acid derivatives and as a building block in medicinal chemistry for developing pharmaceutical agents. Its stability and ease of deprotection make it a versatile reagent in biochemical and pharmaceutical research.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| MP | 135-145 |
| APPEARANCE | White to off white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | £7.46 |
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| 25.000 | 10-20 days | £27.59 |
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| 100.000 | 10-20 days | £78.48 |
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| 500.000 | 10-20 days | £277.28 |
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L-Alanine benzyl ester hydrochloride
L-Alanine benzyl ester hydrochloride is primarily used in the synthesis of peptides and other organic compounds. It serves as a protected form of alanine, where the benzyl ester group safeguards the carboxyl functionality during chemical reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Additionally, it is employed in the preparation of amino acid derivatives and as a building block in medicinal chemistry for developing pharmaceutical agents. Its stability and ease of deprotection make it a versatile reagent in biochemical and pharmaceutical research.
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