Boc-AEEA-OH.DCHA CAS 560088-79-1
Product Name:Boc-AEEA-OH.DCHA
CAS NO.:560088-79-1
Appearance:White powder
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Description
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Products Description

| Product name | Boc-AEEA-OH.DCHA |
| CAS NO. | 560088-79-1 |
| Purity | >99% |
| Alcohol | without alcohol |
| Packaging Type | PP bag /cardboard bucket |
| Material | pharmaceutical intermediates |
| Sheet Size | 1kg/10kg/20kg/100kg |
| Prodcut Weight | 1.2kg/12kg/23kg/115kg |
| Counts | 1kg/bag 10kg/bucket 20kg/bucket 100kg/bucket |
| Certifications | ISO9001 |
| Shelf life | 24 month |
| MOQ | 100 g |
Functions
Boc-AEEA-OH · DCHA (CAS: 560088-79-1) is a functional block of significant value in advanced pharmaceutical chemistry synthesis, and its unique molecular design makes it a key intermediate for constructing complex therapeutic agents. This compound exists in the form of DCHA (dicyclohexylamine) salt, significantly enhancing its physical and chemical stability, making it easy to store and handle. It is particularly suitable for the large-scale production process of cutting-edge peptide drugs such as semaglutide, tilpotide, ritaglutide, and long-acting growth hormone.
The core function of this molecule lies in its dual chemical interactions. One end of it is shielded by a Boc (tert butoxycarbonyl) protecting group, which is stable under alkaline and neutral conditions and can be selectively removed under mild acidic conditions, providing a solid foundation for achieving orthogonal protection strategies in multi-step synthesis. The other end is a carboxyl group that can be connected to the target molecule, and the two are linked through hydrophilic AEEA segments. This structure makes it an excellent "invisible" PEGylation reagent that can efficiently introduce protected PEG like segments into target molecules, serving as functionalized linking arms in complex organic synthesis sequences.
At the application level, the value of Boc-AEEA-OH · DCHA spans across multiple cutting-edge fields. In innovative drug development, it is the core module for designing and constructing novel drug molecules. Through its introduction of flexible hydrophilic spacer arms, it effectively improves the solubility of candidate compounds, reduces aggregation tendency, and optimizes their pharmacokinetic properties. In the field of biotechnology, this compound is a valuable tool for synthesizing various biological conjugates (such as antibody drug conjugates ADC linkers) and precision diagnostic reagents, providing a key chemical means for developing targeted therapies and molecular diagnostic products.
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