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Available Variants1 g
CHA.71748-1g
Price
€346.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.71748-1g | €346.40 |
≥95.0% (HPLC)
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C27H34N2O6 |
|---|---|
| CAS Number | 203854-47-1 |
| Molecular Weight | 482.57 |
| UNSPSC Code | 12352209 |
| NACRES | NA.26 |
| PubChem Substance ID | 57651132 |
| MDL number | MFCD01863054 |
| Beilstein/REAXYS Number | 8022293 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
Fmoc-β-Homolys(Boc)-OH, with a CAS number of 203854-47-1, is a protected amino acid derivative commonly utilized in peptide synthesis. The Fmoc group, or 9-fluorenylmethyloxycarbonyl, serves as a base-labile protecting group for the alpha-amino moiety, while the Boc, or tert-butoxycarbonyl, protects the epsilon-amino group of the lysine side chain. This compound is particularly useful in the synthesis of peptides containing lysine residues, as it allows for the selective deprotection and modification of the epsilon-amino group. The incorporation of Fmoc-β-Homolys(Boc)-OH into peptide sequences can be achieved through standard solid-phase peptide synthesis protocols, and its use has been reported in various applications, including the synthesis of biologically active peptides and protein-protein interaction studies. The compounds properties and reactivity make it a valuable tool in the field of peptide chemistry.
