Products

4A3-SC8 is a modular, ionizable cationic lipid (pKa ≈ 6.66) that functions as a degradable dendrimer. Structurally, it features a dendritic architecture with a central tertiary amine that is pH-responsive, protonated at endosomal pH to facilitate membrane disruption, while remaining neutral in the bloodstream to enhance circulation. The inclusion of hydrolytically degradable ester linkages in its structure and thioether bonds in its tails renders it biodegradable, improving its safety profile for in vivo use. This combination of structural features makes it a highly versatile and robust ionizable lipid for the formulation of LNPs.

The product is β-Alanine, N-[3-(dimethylamino)propyl]-N-[3-[2-(dodecyldithio)ethoxy]-3-oxopropyl]-, 2-(dodecyldithio)ethyl ester, a glutathione-sensitive ionizable lipid built on a β-alanine scaffold that carries three functionally distinct domains: a pendant N,N-dimethylaminopropyl group that provides the primary protonation site, a 2-(dodecyldithio)ethyl ester moiety that anchors one reducible C12 tail through the carboxyl terminus, and an N-linked 3-[2-(dodecyldithio)ethoxy]-3-oxopropyl arm that introduces a second dodecyldisulfanyl chain. This dual-disulfide design ensures that the intact lipid remains stably integrated within the lipid nanoparticle during extracellular transit but undergoes rapid fragmentation into three small, water-soluble fragments upon exposure to the millimolar glutathione concentrations of the cytosol, thereby achieving cargo release that is chemically gated by intracellular redox potential.

The product is β-Alanine, N,N',N''-(nitrilotri-2,1-ethanediyl)tris[N-methyl-, 1,1',1''-tritridecyl ester (commonly known as 304O13). Structurally, it is an ionizable cationic lipidoid, characterized by a central tertiary amine core (nitrilotri-2,1-ethanediyl) linked via three arms to N-methyl-β-alanine units, each terminating in a long, saturated tridecyl (C13) alkyl chain. This unique molecular architecture is meticulously designed for its function: the central amine provides pH-dependent ionization (cationic at low pH, neutral at physiological pH), the amide linkages offer biodegradability, and the three hydrophobic tails drive self-assembly into lipid nanoparticles (LNPs).

C13-112-tetra-tail (CAS 1381861-92-2) is an ionizable cationic lipid molecule characterized by a unique molecular architecture that combines a polar amino alcohol head group, four hydrophobic carbon‑13 tails, and a PEG2 linker. The lipid features a central tertiary amine core from which four tridecyl (C13) chains extend, each terminating in a primary hydroxyl group. Structurally, C13-112-tetra-tail comprises two amino alcohol units connected via a PEG2 (diethylene glycol) spacer, resulting in a symmetric, multi‑tail configuration that maximizes hydrophobic volume while maintaining amphiphilicity for effective lipid nanoparticle (LNP) formation.

1-[2,3-Bis[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]propyl]pyrrolidine, also known as A-066, is a cationic lipid featuring a pyrrolidine head group attached to a glycerol backbone that is di-etherified with two linoleyl (C18:2, Δ9,12) hydrocarbon tails. Structurally, the molecule comprises a central chiral glycerol scaffold with two unsaturated fatty alcohol chains (each containing two cis-double bonds) linked via ether bonds, terminating in a tertiary pyrrolidine amine. The presence of the pyrrolidine head group distinguishes 1-[2,3-Bis[(9Z,12Z)-octadeca-9,12-dien-1-yloxy]propyl]pyrrolidine from the structurally related DODMA, which features a dimethylamino head group.

The product is 2'-F-Ac-dC Phosphoramidite (5'-O-(4,4'-Dimethoxytrityl)-2'-fluoro-2'-deoxycytidine-3'-O-[(2-cyanoethyl)-(N,N-diisopropyl)]-phosphoramidite). As a specialized phosphoramidite monomer, its core structure features a 2'-deoxycytidine sugar moiety with a fluorine atom at the 2' position and an acetyl (Ac) protecting group on the cytosine base. This unique 2'-fluoro modification profoundly influences the sugar pucker conformation, locking the ribose ring into a C3'-endo (RNA-like) conformation. This pre-organized structure dramatically enhances the nuclease resistance of the resulting oligonucleotide and increases its binding affinity to complementary RNA targets. 2'-F-Ac-dC Phosphoramidite is therefore not just a building block; it is the key to generating chemically stabilized, high-affinity antisense oligonucleotides (ASOs), siRNAs, and aptamers.