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Fmoc-Dab(ivDde)-OH This orthogonally-protected diaminobutyric acid derivative is based on the hindered Dde variant ivDde. The side-chain ivDde group is considerably more stable to piperidine than Dde and is less prone to migrate from protected to unprotected side-chains and from side-chain to γ-amino group.When removing ivDde in the presence of allyl-based protecting groups, allyl alcohol should be included in the deprotection solution to prevent reduction of the allyl group. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-Dab(ivDde)-OH, N-α-Fmoc-N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-diaminobutanoic acid. Product Category: Amino Acids. CAS No. 607366-21-2. Mole weight: 546.65. Product ID: ACM607366212. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
N-alpha-Fmoc-Nγ-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-2,4-diaminobutyric acid N-alpha-Fmoc-Nγ-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-2,4-diaminobutyric acid. Group: Biochemicals. Alternative Names: Fmoc-L-Dab(ivDde)-OH. Grades: Highly Purified. CAS No. 607366-21-2. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. USBiological 7
Worldwide
Nα-Fmoc-Nγ-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-2,4-diaminobutyric acid Synonyms: Fmoc-L-Dab(ivDde)-OH; (S)-2-((((9H-Fluoren-9-Yl)Methoxy)Carbonyl)Amino)-4-((1-(4,4-Dimethyl-2,6-Dioxocyclohexylidene)-3-Methylbutyl)Amino)Butanoic Acid; (2S)-4-{[1-(4,4-Dimethyl-2,6-Dioxocyclohexylidene)-3-Methylbutyl]Amino}-2-({[(9H-Fluoren-9-Yl)Methoxy]Carbonyl}Amino)Butanoic Acid. Grades: ≥ 99.9% (Chiral HPLC). CAS No. 607366-21-2. Molecular formula: C32H38N2O6. Mole weight: 546.60. BOC Sciences 4

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