1-(Fmoc-amino)cyclopentanecarboxylic acid
98%
- Product Code: 105169
Alias:
Fmoc-cycloleucine
CAS:
117322-30-2
| Molecular Weight: | 351.4 g./mol | Molecular Formula: | C₂₁H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01074696 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
1-(Fmoc-amino)cyclopentanecarboxylic acid is primarily used in peptide synthesis as a protecting group for amino acids. The Fmoc (fluorenylmethyloxycarbonyl) group shields the amino group during the peptide chain assembly, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build complex peptides. The cyclopentane ring in its structure provides steric stability, enhancing the efficiency of the synthesis process. After the peptide is fully assembled, the Fmoc group can be easily removed under mild basic conditions, making it a versatile and widely used reagent in biochemistry and pharmaceutical research. Its application extends to the production of therapeutic peptides, protein studies, and drug development.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿980.00 |
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| 5.000 | 10-20 days | ฿1,620.00 |
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1-(Fmoc-amino)cyclopentanecarboxylic acid
1-(Fmoc-amino)cyclopentanecarboxylic acid is primarily used in peptide synthesis as a protecting group for amino acids. The Fmoc (fluorenylmethyloxycarbonyl) group shields the amino group during the peptide chain assembly, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build complex peptides. The cyclopentane ring in its structure provides steric stability, enhancing the efficiency of the synthesis process. After the peptide is fully assembled, the Fmoc group can be easily removed under mild basic conditions, making it a versatile and widely used reagent in biochemistry and pharmaceutical research. Its application extends to the production of therapeutic peptides, protein studies, and drug development.
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