11-[(tert-Butoxycarbonyl)amino]undecanoic Acid
≥98%
- Product Code: 104435
CAS:
10436-25-6
| Molecular Weight: | 301.43 g./mol | Molecular Formula: | C₁₆H₃₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00076902 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active molecules. It serves as a key intermediate for introducing amino groups into long-chain molecules, which is essential in designing compounds with specific properties. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, ensuring selective reactions can occur at other sites of the molecule. This is particularly useful in peptide synthesis, where protecting groups are necessary to control the assembly of amino acids in a specific sequence. Additionally, it can be employed in the development of surfactants, lubricants, or other materials that benefit from the incorporation of long aliphatic chains with functionalized end groups. Its versatility makes it valuable in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White - Off White Powder |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $20.40 |
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| 5.000 | 10-20 days | $89.71 |
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| 25.000 | 10-20 days | $281.43 |
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11-[(tert-Butoxycarbonyl)amino]undecanoic Acid
This compound is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active molecules. It serves as a key intermediate for introducing amino groups into long-chain molecules, which is essential in designing compounds with specific properties. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino functionality, ensuring selective reactions can occur at other sites of the molecule. This is particularly useful in peptide synthesis, where protecting groups are necessary to control the assembly of amino acids in a specific sequence. Additionally, it can be employed in the development of surfactants, lubricants, or other materials that benefit from the incorporation of long aliphatic chains with functionalized end groups. Its versatility makes it valuable in both academic research and industrial applications.
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