L-(+)-Fmoc-ornithine hydrochloride is a derivative of the amino acid ornithine, characterized by the presence of a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), due to its ability to protect the amino group while allowing for further coupling reactions. The Fmoc group is easily removed under basic conditions, facilitating the sequential addition of amino acids. L-(+)-Fmoc-ornithine itself is a chiral molecule, with the L-configuration being biologically relevant. As a hydrochloride salt, it is soluble in water and polar organic solvents, making it suitable for various biochemical applications. The compound's molecular structure includes a secondary amine, which contributes to its reactivity in peptide formation. Additionally, L-(+)-Fmoc-ornithine hydrochloride is often used in the synthesis of bioactive peptides and in research involving protein engineering and drug development. Its stability and ease of handling make it a valuable reagent in organic and medicinal chemistry.

L-(+)-Fmoc-ornithine hydrochloride

201046-57-3: (2S)-5-amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)pentanoic acid hydrochloride, Fmoc-Orn-OH・HCl

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-aminopentanoic acid hydrochloride

Fmoc-Orn-OH · HCl

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CAS 201046-57-3: L-(+)-Fmoc-ornithine hydrochloride

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-aminopentanoic acid hydrochloride

Ref: 10-F223997

Fmoc-Orn-OH · HCl

Ref: 01-4025982

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-aminopentanoic acid hydrochloride

Ref: 54-OR75129

Fmoc-Nd-L-ornithine hydrochloride

Ref: 3D-FN48602

L-Ornithine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-, hydrochloride (1:1)

Ref: IN-DA002D6A