| Field | Specification |
|---|---|
| Activity | |
| Alternative Names | n-Octadecanoyl Coenzyme A |
| Form | Lyophilized powder |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in water |
| Storage |
Overview
Stearoyl Coenzyme A, Sodium salt is a biochemical supplied by Coenza for use in enzymology and metabolic research. Available as Lyophilized powder, purity ≥ 95%, suitable for in vitro assays and pathway studies.
Also known as: n-Octadecanoyl Coenzyme A.
Key Elements and Design Rationale
- Formula / MW / Purity: C39H67N7O17P3S · xNa; 1034.00 g/mol (free acid basis); ≥ 95%. The Sodium salt form provides enhanced aqueous stability.
- Form / Solubility: Lyophilized powder; Soluble in water.
- Synonyms: n-Octadecanoyl Coenzyme A.
- Origin: Biosynthetic synthesis.
Biological Background
Stearoyl coenzyme A (Stearoyl-CoA) is a saturated fatty acid metabolite which plays a key role in polyunsaturated fatty acid synthesis and the PPAR signaling pathway. Stearoyl-CoA is a primary substrate for stearoyl-CoA desaturase, an enzyme that converts it into oleoyl-CoAa vital step in the production of monounsaturated fatty acids. This conversion is essential for maintaining lipid homeostasis, influencing membrane fluidity, and regulating metabolic signaling pathways (Paton & Ntambi, 2009; Zeng et al., 2023).
Research Relevance and Current Trends
- Acyl-CoA metabolism increasingly linked to histone acylation marks and epigenetic regulation in cancer and metabolic disease research.
- Growing interest in short-chain fatty acid CoA thioesters as mediators of gut microbiome–host metabolic crosstalk.
- CoA-dependent enzymes investigated as drug targets in infectious disease and neurometabolic disorder research.
Common Research Applications
- Enzyme kinetics assays — direct substrate for acyltransferases, thiolases, and dehydrogenases.
- Metabolic flux analysis — isotope-labeled variants available for stable-isotope tracing.
- In vitro pathway reconstitution for fatty acid β-oxidation, TCA cycle, or polyketide biosynthesis.
- Biochemical characterization of CoA-binding proteins by activity assays or binding measurements.
Notes for Experimental Interpretation
- CoA thioesters hydrolyze at neutral–alkaline pH; prepare working solutions fresh and keep on ice.
- Different salt forms share the same core structure — normalize concentrations using the free-acid MW when comparing across forms.
- Thiol oxidation may occur upon air exposure; use under inert atmosphere or with reducing agents where appropriate.
Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.
- Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
- Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
- Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
- QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
- Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity
To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).
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equivalents, or discuss custom synthesis with the right QC documentation (RUO).
Paton, C. M., & Ntambi, J. M. (2009). Biochemical and physiological function of stearoyl-CoA desaturase. American Journal of Physiology-Endocrinology and Metabolism, 297(1), E28–E37.
Zeng, X., Wang, X., Xu, J., Wang, Y., & Guo, Y. (2023). Stearoyl-CoA desaturase and its roles in inflammatory responses and diseases. Cellular & Molecular Immunology, 20, 428–439.
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