Fmoc chloride
For HPLC derivatization, ≥99.0% (HPLC)
- Product Code: 93705
Alias:
Fluorenylmethyloxycarbonyl chloride; 9-fluorenylmethyl chloroformate, 9-fluorenylmethyloxycarbonyl chloride, 9-fluorenylmethyl chloroformate
CAS:
28920-43-6
| Molecular Weight: | 258.7 g./mol | Molecular Formula: | C₁₅H₁₁ClO₂ |
|---|---|---|---|
| EC Number: | 249-313-6 | MDL Number: | MFCD00001138 |
| Melting Point: | 62-64 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Fmoc chloride is widely used in peptide synthesis as a protecting group for amino acids. It reacts with the amino group to form an Fmoc-protected amino acid, which prevents unwanted side reactions during peptide chain assembly. This protection is crucial in solid-phase peptide synthesis (SPPS), where the Fmoc group can be easily removed under mild basic conditions, allowing for sequential addition of amino acids. Its stability and selective deprotection make it a preferred choice in the production of complex peptides and proteins for pharmaceutical and biochemical research. Additionally, Fmoc chloride is employed in the synthesis of other organic compounds where temporary protection of amine groups is required.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 60 65? |
| PURITYHPLC | 99 100% |
| APPEARANCE | WHITE TO YELLOW POWDER OR CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,120.00 |
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| 1.000 | 10-20 days | ฿4,100.00 |
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| 5.000 | 10-20 days | ฿11,600.00 |
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| 25.000 | 10-20 days | ฿32,800.00 |
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| 100.000 | 10-20 days | ฿82,000.00 |
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| 500.000 | 10-20 days | ฿123,000.00 |
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Fmoc chloride
Fmoc chloride is widely used in peptide synthesis as a protecting group for amino acids. It reacts with the amino group to form an Fmoc-protected amino acid, which prevents unwanted side reactions during peptide chain assembly. This protection is crucial in solid-phase peptide synthesis (SPPS), where the Fmoc group can be easily removed under mild basic conditions, allowing for sequential addition of amino acids. Its stability and selective deprotection make it a preferred choice in the production of complex peptides and proteins for pharmaceutical and biochemical research. Additionally, Fmoc chloride is employed in the synthesis of other organic compounds where temporary protection of amine groups is required.
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