Fmoc Boc CBZ tBu

Linkers with protecting groups are bifunctional molecules featuring temporarily masked reactive sites (e.g., Fmoc, Boc, Cbz, and tBu) that can be selectively deprotected under specific conditions. They enable sequential and orthogonal conjugation in complex syntheses—such as peptide assembly, solid-phase chemistry, and prodrug development—by preventing side reactions and ensuring precise structural control. These regulated deprotection capabilities make them indispensable tools in advanced organic synthesis, bioconjugation, and therapeutic agent development.

 Item #CAS #M.F M.W
Boc-PEG3-NHS ester 4327803 2250216-93-2 C18H30O9N2 418.44
 Item #CAS #M.F M.W
HOOC-CH2-PEG4-CH2CH2COOtBu 431804 2304558-22-1 C17H32O9 380.43
 Item #CAS #M.F M.W
HOOC-CH2-PEG8-CH2CH2COOtBu 431808 3052794-63-2 C25H48O13 556.65
 Item #CAS #M.F M.W
BocNH-PEG4-CH2CH2Br 4324904 1392499-32-9 C15H30BrNO6 400.31
 Item #CAS #M.F M.W
BocNH-PEG7-CH2CHN3 4326307 N/A C21H42N4O9 494.58
 Item #CAS #M.F M.W
H2N-PEG1-CH2COOtBu 4328201 1155811-37-2 C8H17NO3 175.23
 Item #CAS #M.F M.W
N3-PEG3-CH2COOtBu 438803 172531-36-1 C12H23N3O5 289.33
 Item #CAS #M.F M.W
N3-PEG4-CH2CH2COOtBu 436804 581066-04-8 C15H29N3O6 347.41
 Item #CAS #M.F M.W
H2N-PEG24-CH2CH2COOtBu·HCl 4328524 2170987-96-7 C55H111NO26·HCl 1202.46
 Item #CAS #M.F M.W
H2N-PEG36-CH2CH2COOtBu·HCl 4328536 N/A C79H159NO38·HCl 1731.09
 Item #CAS #M.F M.W
H2N-PEG45-CH2CH2COOtBu·HCl 4328545 N/A C97H195NO47·HCl 2127.56
 Item #CAS #M.F M.W
Fmoc-PEGO-OH 4334102 916585-44-9 C29H38N2O9 558.62