
5A2-SC8
Chemical Name
2-[3-[2-[2-[2-[2-[bis[3-[2-(2-methyl-3-octylsulfanylpropanoyl)oxyethoxy]-3-oxopropyl]amino]ethylamino]ethyl-[3-[2-(2-methyl-3-octylsulfanylpropanoyl)oxyethoxy]-3-oxopropyl]amino]ethylamino]ethyl-[3-[2-(2-methyl-3-octylsulfanylpropanoyl)oxyethoxy]-3-oxopropyl]amino]propanoyloxy]ethyl 2-methyl-3-octylsulfanylpropanoate
5A2-SC8•LNP
Structure: 

Product No
CH51066
CAS
1857341-90-2
MF
C93H173N5O20S5
MW
1841.72
Specification
| Catalog No. | CH51066 |
| CAS No. | 1857341-90-2 |
| Molecular Formula | C93H173N5O20S5 |
| Molecular Weight | 1841.72 |
CHEMOS Support for This Category
CHEMOS supports custom synthesis and process development for LNP lipid components, with work planned according to target structure, requested scale, and analytical requirements. Ionizable lipid route development : route scouting, impurity review, stereochemistry control, and purification planning. Helper lipid and PEG-lipid preparation : support for phospholipids, sterol-related components, PEG-lipids, and related analogs. Analytical support : HPLC, NMR, MS, Karl Fischer water content, elemental analysis, and residual-solvent testing can be discussed by project. Scale-up support : transfer from laboratory preparation to larger pilot or production batches after route and quality review. Project documentation : batch-specific COA and technical information are provided according to the confirmed specification.
Overview
5A2-SC8 (CAS 1857341-90-2, MF C93H173N5O20S5, MW 1841.72) belongs to the ionizable lipid class used in LNP delivery system research for mRNA, siRNA and gene-editing cargos. Programs working with this compound usually examine the head-group / tail combination, related-substance profile, and stereochemistry. Bench-scale to larger-scale production is supported through CHEMOS organic chemistry workflows and dedicated process-development resources.
Applications
- 5A2-SC8 (1857341-90-2) supply and analog preparation for research programs
- Ionizable lipid library and head-group / tail analog screening
- Custom analog synthesis with controlled head-group and tail variants
- Analytical method development for ionizable lipid related substances
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