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A0CB7289-1Z
Thomas Scientific
Fmoc-DAP(Boc)-OH; N-Fmoc-N-Boc-(S)-2,3-diaminopropionic acid; CAS Number: 162558-25-0 (C08-0139-164)
Price: $202.95List Price: $225.50Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA) -
A0CB7289-5Z
Thomas Scientific
Fmoc-DAP(Boc)-OH; N-Fmoc-N-Boc-(S)-2,3-diaminopropionic acid; CAS Number: 162558-25-0 (C08-0140-312)
Price: $649.45List Price: $721.62Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA) -
A0FW4550-1Z
Thomas Scientific
Fmoc-Dihydro-Trp(Boc)-OH; Fmoc-Dihydro-N-in-t-butyloxycarbonyl-L-tryptophan; CAS Number: (C08-0138-468)
Price: $115.97List Price: $128.85Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA) -
8520870005Standard building block for introduction of diaminopropionic acid amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1201 Analysis Note Color
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8522160001An excellent derivative for the chemoselective ligation of unprotected peptides in aqueous media [1] via oxime formation. This derivative introduces a hydroxylamine functionality which can couple with aldehyde groups present in another peptide unit.
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8522160025An excellent derivative for the chemoselective ligation of unprotected peptides in aqueous media [1] via oxime formation. This derivative introduces a hydroxylamine functionality which can couple with aldehyde groups present in another peptide unit.
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8522160005An excellent derivative for the chemoselective ligation of unprotected peptides in aqueous media [1] via oxime formation. This derivative introduces a hydroxylamine functionality which can couple with aldehyde groups present in another peptide unit.
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8520530001Standard building block for introduction of aminohexanoic amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1111 Analysis Note Color (visual):
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8520530025Standard building block for introduction of aminohexanoic amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1111 Analysis Note Color (visual):
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8520530005Standard building block for introduction of aminohexanoic amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1111 Analysis Note Color (visual):
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8520430001Standard building block for introduction of gamma aminobutyric acid amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1088 Analysis Note Color
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8521200001A superior derivative to Fmoc-Gln(Trt)-OH for the synthesis of Gln-containing peptides by Fmoc SPPS. Fmoc-Gln(Dmcp)-OH is more soluble in DMF than Fmoc-Gln(Trt)-OH, thereby facilitating coupling reactions at higher concentration.