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Boc-β-(3-pyridyl)-Ala-OH

Boc-β-(3-pyridyl)-Ala-OH

Boc-β-(3-pyridyl)-Ala-OH (Boc-3-(3-pyridyl)-L-alanine) is a Boc-protected unnatural amino acid featuring a 3-pyridyl group at the β-position of the alanine backbone. The molecule consists of an L-alanine core with a tert-butyloxycarbonyl (Boc) protecting group on the α-amino group, a free carboxylic acid at the C-terminus, and a 3-pyridyl substituent replacing the methyl group of natural alanine.
Boc-D-Phe-Pro-Arg-Pro-OH.HCl

Boc-D-Phe-Pro-Arg-Pro-OH.HCl

Boc-D-Phe-Pro-Arg-Pro-OH.HCl is a protected tetrapeptide consisting of four amino acid residues in the sequence D-Phe-Pro-Arg-Pro, with a tert-butyloxycarbonyl (Boc) protecting group at the N-terminus and the C-terminus as the free carboxylic acid, stabilized as the hydrochloride salt.
H-D-Lys(Boc)-OtBu.HC

H-D-Lys(Boc)-OtBu.HC

H-D-Lys(Boc)-OtBu.HCl is an orthogonally protected D-lysine derivative featuring a free α-amino group stabilized as the hydrochloride salt, a tert-butyloxycarbonyl (Boc) protecting group on the ε-amino side chain, and a tert-butyl ester (OtBu) at the C-terminus.
Boc-Lys(Boc)-ONp

Boc-Lys(Boc)-ONp

Boc-Lys(Boc)-ONp (Nα,ε-di-Boc-L-lysine 4-nitrophenyl ester) is a doubly protected lysine derivative featuring Boc protecting groups on both the α-amino and ε-amino groups, with a 4-nitrophenyl (ONp) ester activating the C-terminus. 
H-N-Me-Trp(Boc)-OAll Oxalate

H-N-Me-Trp(Boc)-OAll Oxalate

H-N-Me-Trp(Boc)-OAll Oxalate (tert-butyl (S)-3-(3-(allyloxy)-2-(methylamino)-3-oxopropyl)-1H-indole-1-carboxylate oxalate) is a specialized N-methylated tryptophan derivative featuring orthogonal protection of its three functional groups. The molecule incorporates an Nα-methyl group (H-N-Me), a Boc-protected indole nitrogen, and an allyl ester (OAll) protecting group at the C-terminus.
Boc-Val-OH

Boc-Val-OH

Boc-Val-OH (N-(tert-Butoxycarbonyl)-L-valine) is a Boc-protected derivative of the essential branched-chain amino acid L-valine. The molecule consists of a valine core with its α-amino group protected by a tert-butoxycarbonyl (Boc) group, while the carboxylic acid remains free for coupling reactions. This protection strategy renders the amino group inert under basic and nucleophilic conditions while allowing selective deprotection under acidic conditions (typically TFA).
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