FMOC-DAP HCl, or 9-fluorenylmethoxycarbonyl-2,3-diaminopropionic acid hydrochloride, is a chemical compound commonly used in peptide synthesis and research. It features a protective FMOC group, which is a popular choice for protecting amine functionalities during the synthesis of peptides. The presence of the diaminopropionic acid moiety allows for the introduction of additional functional groups, enhancing the versatility of the compound in various chemical reactions. As a hydrochloride salt, FMOC-DAP HCl is typically more stable and soluble in aqueous solutions compared to its free base form. This compound is characterized by its ability to undergo deprotection under mild conditions, making it suitable for sequential peptide synthesis. Additionally, FMOC-DAP HCl can be utilized in the development of bioactive peptides and in the study of protein interactions. Its structural features contribute to its utility in both academic and pharmaceutical research settings, particularly in the fields of medicinal chemistry and biochemistry.

FMOC-DAP HCL

210767-37-6: N-Fmoc-1,3-diaminopropane HCl, Fmoc-1,3-diaminopropane hydrochloride

CAS 210767-37-6: FMOC-DAP HCL

Fmoc-DAP.HCl

Ref: 10-F330581

Fmoc-DAP.HCl

Ref: 54-BIBP1039

Carbamic acid, N-(3-aminopropyl)-, 9H-fluoren-9-ylmethyl ester, hydrochloride (1:1)

Ref: IN-DA002KYH

Fmoc-DAP.HCl

Ref: 3D-KIA76737