Butyryl Coenzyme A, Lithium Salt

SKU:BHB21200012
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Coenza
Coenza
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Overview
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Butyryl Coenzyme A, Lithium Salt (Lithium salt) is a coenzyme A thioester derivative (C25H39N7O17P3S · xLi; MW 837.62 g/mol (free acid basis)) supplied as Lyophilized powder, purity ≥ 95%, water-soluble. Used as an enzyme substrate/cofactor in metabolic research, enzyme kinetics, and in vitro reconstitution of CoA-dependent pathways.
Purity ≥ 95%
Form Lyophilized powder
Molecular Weight 837.62 g/mol (free acid basis)
Solubility Soluble in water
Source Biosynthetic
Activity Enzyme Substrate / Cofactor
Options selector
Catalog no. Size
A-22-10MG 10 mg
Available Options

Available Sizes:

  • 10 mg

Shipping: Ambient temperature (styrofoam + ice gels) — shipped on ice packs at ambient temperature (styrofoam + ice gels). Store at −20 °C upon receipt.

Field Specification
Mfr No A-22
Activity
  • Enzyme Substrate / Cofactor
Alternative Names Coenzyme A, S-butanoate, lithium salt
Coenzyme A Class Short-chain
Form Lyophilized powder
Molecular Weight 837.62 g/mol (free acid basis)
Product Type
  • Biochemicals
  • Small Molecules
Purity ≥ 95%
Shipping Ambient temperature (styrofoam + ice gels)
SMILES O=C(CCNC(C(C(C)(COP([O-])(OP([O-])(OCC(C(C1O)OP(O)([O-])=O)OC1N(C2=NC=N3)C=NC2=C3N)=O)=O)C)O)=O)NCCSC(CCC)=O.[Li+]
Solubility Soluble in water
Storage -20°C

Overview

Butyryl Coenzyme A, Lithium 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: Coenzyme A, S-butanoate, lithium salt.

Key Elements and Design Rationale

  • Formula / MW / Purity: C25H39N7O17P3S · xLi; 837.62 g/mol (free acid basis); ≥ 95%. The Lithium salt form provides enhanced aqueous stability.
  • Form / Solubility: Lyophilized powder; Soluble in water.
  • Synonyms: Coenzyme A, S-butanoate, lithium salt.
  • Origin: Biosynthetic synthesis.

Biological Background

Butanoyl Coenzyme A (Butanoyl-CoA), also known as butyryl-CoA, is a thioester of Coenzyme A that plays a crucial role in fatty acid metabolism and energy production. It is formed as an intermediate during the ?-oxidation of fatty acids and serves as a substrate for various enzymes involved in lipid metabolism and biosynthetic pathways. Butanoyl-CoA is important in the synthesis of butyrate, a short-chain fatty acid that is a key energy source for colonocytes and has significant roles in maintaining gut health and modulating inflammatory responses. It also functions as an acyl donor in the elongation and degradation of fatty acids, making it a critical intermediate in cellular metabolism (Vital et al., 2017; Louis & Flint, 2017).

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.
What is Butyryl Coenzyme A, Lithium Salt and what is it used for?
Butyryl Coenzyme A, Lithium Salt is a coenzyme A thioester derivative (MW 837.62 g/mol (free acid basis), C25H39N7O17P3S · xLi) supplied as Lyophilized powder, purity ≥ 95%. The Lithium salt form offers improved aqueous stability compared with some alternatives. It is used as an enzyme substrate and cofactor in metabolic research, enzyme kinetics, and in vitro reconstitution of CoA-dependent biosynthetic and catabolic pathways.
What are the key physicochemical properties?
Molecular formula: C25H39N7O17P3S · xLi; MW: 837.62 g/mol (free acid basis); purity: ≥ 95%; form: Lyophilized powder; solubility: Soluble in water; stability: ≥ 2 years. The reactive thioester bond is susceptible to hydrolysis — prepare working solutions fresh and keep on ice during experiments.
How should Butyryl Coenzyme A, Lithium Salt be dissolved for biochemical assays?
This product is Soluble in water. Dissolve in the appropriate aqueous buffer at the required pH immediately before use. For stock solutions, aliquot into single-use volumes, snap-freeze in liquid nitrogen, and store at −20 °C. Avoid repeated freeze-thaw cycles to prevent hydrolysis.
What enzymes or metabolic pathways is this compound most relevant to?
Depending on the acyl chain length and structure, CoA thioester derivatives serve as substrates for acyl-CoA synthetases, acyltransferases, thiolases, acyl-CoA dehydrogenases, carboxylases, and mutases. Relevant pathways include fatty acid β-oxidation, TCA cycle, amino acid catabolism, and polyketide or terpenoid biosynthesis. Refer to the General Information section and the cited literature for compound-specific enzyme associations.
Does the salt form matter for experimental design?
The salt form (Free Acid, Lithium, Sodium, Trilithium, Trisodium) shares the same core acyl-CoA structure. Counterions are typically inert at standard assay concentrations. When preparing solutions, use the free-acid MW (837.62 g/mol (free acid basis)) to normalize molar concentrations across salt forms. Verify buffer compatibility if high ionic strength is a concern.

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).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

Vital, M., Howe, A. C., & Tiedje, J. M. (2017). Revealing the bacterial butyrate synthesis pathways by analyzing (meta)genomic data. mBio, 8(2), e00889-17.

Louis, P., & Flint, H. J. (2017). Formation of propionate and butyrate by the human colonic microbiota. Environmental Microbiology, 19(1), 29-41.

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