Lipids & Polymers

14(Z)-Tricosenol

15(Z)-Tetracosenol

Benzyloxy carbonyl-PEG12-t-butyl ester is a heterobifunctional linker comprised of a benzyloxy carbonyl where the benzyl protecting group can be removed by hydrogenolysis and t-butyl ester can be deprotected under acidic conditions. The PEG12 chain improves the molecule's hydrophilicity.

N-Mal-N-bis(PEG8-NH-Boc) serves as a branched PEG linker consisting of two Boc groups which can be removed under acidic conditions to free the amine for further reactions. The maleimide attached to the central amine of the molecule can react directly with thiol-bearing entities to form a covalent bond.

N-Mal-N-bis(PEG8-amine) functions as a branched PEG linker with two terminal amine groups that are reactive with active succinimidyl ester. The maleimide group linked to the central amine forms a covalent bond with thiol-bearing molecules.

1,2-Dioleoyl-sn-glycero-3-PEG2-Azide is characterized by two oleic acid unsaturated fatty acid tails and an azide head group which acts as a click chemistry handle that is used to react with terminal alkynes or strained cyclooctynes such as DBCO, BCN.

1,2-Dioleoyl-sn-glycero-3-PEG4-Azide is a click-chemistry lipid that contains a pair of oleic acid unsaturated fatty acid tails and an azide click chemistry handle that readily reacts with strained cyclooctynes and terminal alkynes. The PEG4 chain imparts hydrophilicity.

1,2-Dioleoyl-sn-glycero-3-PEG8-Azide functions as a click-chemistry lipid with two oleic acid unsaturated fatty acid tails and an azide head group to perform click reactions with DBCO, BCN, alkyne. The PEG units enhance the overall water solubility of the compound.

1,2-Dioleoyl-sn-glycero-3-PEG12-Azide is described by an azide click-chemistry handle at the head and two oleic acid unsaturated fatty acid tails.