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Fmoc-Lys(Dde)-OH CAS 150629-67-7 Orthogonally Protected Amino Acid for Solid Phase Peptide Synthesis

Fmoc-Lys(Dde)-OH CAS 150629-67-7 Orthogonally Protected Amino Acid for Solid Phase Peptide Synthesis

Detail Information
A Single Impurity:
≤0.2%
Assay:
≥98.0%
Cas:
150629-67-7
Safety Level:
S22-24 / 25
Safety Information:
Handle With Appropriate Protective Equipment; Avoid Inhalation And Contact With Skin
Formula Weight:
523.64
Cas Number:
Varies Depending On Specific Protected Amino Acid
Refractive Index:
-24 ° (C = 1, DMF)
Percent Purity:
98%
Appearance:
White To Off-white Crystalline Powder
Solubility:
Soluble In Organic Solvents, Sparingly Soluble In Water
Molecular Weight:
532.64
Molecular Formula:
C₃₁H₃₆N₂O₆
Package:
25kg / Barrel
Relative Density:
Not Available
Highlight:

Fmoc-Lys(Dde)-OH protected amino acid

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Orthogonally protected amino acid for peptide synthesis

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Fmoc-Lys(Dde)-OH CAS 150629-67-7

Product Description

Fmoc-Lys(Dde)-OH is an orthogonally double protected L-lysine derivative with molecular formula C₃₁H₃₆N₂O₆, molecular weight 532.64, CAS 150629-67-7, PubChem CID 135404832. It is a key building block for Fmoc-based solid-phase peptide synthesis (SPPS). The α-amino group is protected by Fmoc group, removable by piperidine, while the ε-amino group is blocked by Dde group, which can be selectively cleaved by hydrazine/DMF without affecting Fmoc. This orthogonal protection enables site-specific side chain modification, branched peptide and cyclic peptide preparation.

Key Benefits:

• Orthogonal dual protecting groups for selective deprotection • Ideal building block for solid phase peptide synthesis (SPPS) • Enables site-specific peptide labelling & side-chain modification • Stable under standard Fmoc peptide synthesis reaction conditions • High purity for pharmaceutical & research peptide development

Target Industries: Peptide Synthesis, Pharmaceutical Intermediates, Biochemical Research, Custom Peptide Manufacturing Applications: Branched Peptides, Cyclic Peptides, Site-Specific Peptide Modification, Biopharmaceutical R&D