L-Isoleucine Benzyl Ester 4-Toluenesulfonate Salt
95%
- Product Code: 105294
Alias:
H-Ile-OBzl tos;(2S,3S)-Benzyl 2-amino-3-methylpentanoate 4-methylbenzenesulfonate
CAS:
16652-75-8
Molecular Weight: | 393.51 g./mol | Molecular Formula: | C₂₀H₂₇NO₅S |
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EC Number: | 240-701-0 | MDL Number: | MFCD00050511 |
Melting Point: | 153-155 °C | Boiling Point: | 545.1 °C at 760 mmHg |
Density: | Storage Condition: | room temperature, inert gas, sealed |
Product Description:
L-Isoleucine Benzyl Ester 4-Toluenesulfonate Salt is primarily used in organic synthesis and peptide chemistry. It serves as a protected form of L-isoleucine, enabling controlled reactions in the construction of peptides and other complex molecules. The benzyl ester group provides stability during synthesis, while the toluenesulfonate salt enhances solubility in various organic solvents. This compound is particularly valuable in the production of custom peptides for pharmaceutical research, where precise amino acid incorporation is critical. Additionally, it is employed in the development of bioactive compounds and in studies exploring enzyme-substrate interactions. Its role in protecting functional groups makes it a versatile reagent in synthetic organic chemistry.
Product Specification:
Test | Specification |
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Appearance | White Powder |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | $70.32 |
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25.000 | 10-20 days | $203.42 |
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L-Isoleucine Benzyl Ester 4-Toluenesulfonate Salt
L-Isoleucine Benzyl Ester 4-Toluenesulfonate Salt is primarily used in organic synthesis and peptide chemistry. It serves as a protected form of L-isoleucine, enabling controlled reactions in the construction of peptides and other complex molecules. The benzyl ester group provides stability during synthesis, while the toluenesulfonate salt enhances solubility in various organic solvents. This compound is particularly valuable in the production of custom peptides for pharmaceutical research, where precise amino acid incorporation is critical. Additionally, it is employed in the development of bioactive compounds and in studies exploring enzyme-substrate interactions. Its role in protecting functional groups makes it a versatile reagent in synthetic organic chemistry.
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