Results for PEG ( 6581 )
- From: £486.00
Azide-PEG-alcohol, MW 3,400 is a click chemistry PEG polymer. Azide undergoes click chemistry with alkyne group, such as DBCO/BCN molecule or teminal alkyne. Hydroxyl functional group can be functionalized further to form halide, aldehyde, carboxylic acid etc. Reagent grade, for research purpose.
- From: £312.00
Fmoc-N-amido-PEG-CH2COOH, MW 2,000 is a Fmoc-protected PEGylation reagent containing a carboxylic acid terminus. The carboxylic acid is readily available for reaction with a primary amine in the presence of HATU or EDC to form a stable amide bond. The Fmoc deprotection results in a terminal amine which can be used for many bioconjugation. Reagent grade, for research purpose.
- From: £673.00
N-Boc-N'-(PEG1-t-butyl ester)-L-Lysine-OH is the amino acid lysine with a Boc-protected α-amine and an amido-PEG1-t-butyl ester on its ε-amine. The carboxylic acid can be reacted with alcohols or amides, while the Boc and a t-butyl ester which can be later deprotected to perform further conjugation.
- From: £934.00
N-bis(Azide-PEG23)-N-(PEG24-Acid) is a branched PEGylation reagent containing an amino group with two azide groups. The amino group is reactive with carboxylic acids, activated NHS esters. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
- From: £1,071.00
N-(Amino-PEG23)-N-bis(PEG23-Azide) is a branched PEGylation reagent containing an amino group with two azide groups. The amino group is reactive with carboxylic acids, activated NHS esters. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
- From: £561.00
N-Boc-N'-(PEG1-t-butyl ester)-L-Lysine-NHS ester is the amino acid lysine with a Boc-protected α-amine, an amido-PEG1-t-butyl ester on its ε-amine, and an NHS ester on its C-terminus. The NHS can be easily displaced by amines to form an amide, while the Boc and t-butyl ester can be deprotected to perform further conjugation.