Boc-L-Methionine
99%
- Product Code: 66117
Alias:
N-tert-butoxycarbonyl-L-methionine; BOC-L-eggamino-DCHA
CAS:
2488-15-5
| Molecular Weight: | 249.33 g./mol | Molecular Formula: | C₁₀H₁₉NO₄S |
|---|---|---|---|
| EC Number: | 219-639-3 | MDL Number: | MFCD00065586 |
| Melting Point: | 47-50 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Boc-L-Methionine is widely used in peptide synthesis as a protecting group for the amino group of methionine. It ensures selective reactions during the formation of peptide bonds, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides. Additionally, it is employed in the preparation of modified peptides and bioactive molecules, where the Boc group can be easily removed under mild acidic conditions without affecting other functional groups. Its stability and compatibility with various chemical reactions make it a preferred choice in organic and medicinal chemistry research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Almost white Crystal - Powder |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿740.00 |
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| 25.000 | 10-20 days | ฿2,480.00 |
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| 100.000 | 10-20 days | ฿9,120.00 |
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| 500.000 | 10-20 days | ฿34,620.00 |
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Boc-L-Methionine
Boc-L-Methionine is widely used in peptide synthesis as a protecting group for the amino group of methionine. It ensures selective reactions during the formation of peptide bonds, preventing unwanted side reactions. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides. Additionally, it is employed in the preparation of modified peptides and bioactive molecules, where the Boc group can be easily removed under mild acidic conditions without affecting other functional groups. Its stability and compatibility with various chemical reactions make it a preferred choice in organic and medicinal chemistry research.
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