Hexanoyl Coenzyme A, Free acid

SKU:BHB21200023
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Coenza
Coenza
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Overview
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Hexanoyl Coenzyme A, Free acid (Free Acid) is a coenzyme A thioester derivative (C27H46N7O17P3S; MW 865.68 g/mol) 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 865.68 g/mol
Solubility Soluble in water
Source Biosynthetic
Activity Enzyme Substrate / Cofactor
Options selector
Catalog no. Size
A-28-10MG 10 mg
A-28-25MG 25 mg
Available Options

Available Sizes:

  • 10 mg
  • 25 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-28
Activity
  • Enzyme Substrate / Cofactor
Alternative Names Hexanoyl-CoA, Caproyl coenzyme A
Coenzyme A Class Short-chain
Form Lyophilized powder
Molecular Weight 865.68 g/mol
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(CCCCC)=O
Solubility Soluble in water
Storage -20°C

Overview

Hexanoyl Coenzyme A, Free acid 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: Hexanoyl-CoA, Caproyl coenzyme A.

Key Elements and Design Rationale

  • Formula / MW / Purity: C27H46N7O17P3S; 865.68 g/mol; ≥ 95%. The Free Acid form provides enhanced aqueous stability.
  • Form / Solubility: Lyophilized powder; Soluble in water.
  • Synonyms: Hexanoyl-CoA, Caproyl coenzyme A.
  • Origin: Biosynthetic synthesis.

Biological Background

Hexanoyl coenzyme A (hexanoyl-CoA) is a medium-chain fatty acyl-CoA that serves as a preferred substrate for ghrelin O-acyltransferase (GOAT) in enzyme assays, outperforming octanoyl-CoA. GOAT, the enzyme responsible for the acylation of ghrelin, exhibits a higher catalytic efficiency with hexanoyl-CoA, which enhances ghrelin's biological activity in regulating appetite and energy balance. Hexanoyl-CoA acts as a biosynthetic precursor to olivetolic acid, a key intermediate in the production of phytocannabinoids such as cannabigerolic acid (CBGA). This makes hexanoyl-CoA a functionally important molecule in both mammalian metabolism and plant secondary metabolite biosynthesis (Yang et al., 2016; Gagne et al., 2012).

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 Hexanoyl Coenzyme A, Free acid and what is it used for?
Hexanoyl Coenzyme A, Free acid is a coenzyme A thioester derivative (MW 865.68 g/mol, C27H46N7O17P3S) supplied as Lyophilized powder, purity ≥ 95%. The Free Acid 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: C27H46N7O17P3S; MW: 865.68 g/mol; 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 Hexanoyl Coenzyme A, Free acid 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 (865.68 g/mol) 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).

Yang, J., Zhao, T.-J., Goldstein, J.L., & Brown, M.S. (2016). Inhibition of ghrelin O-acyltransferase suppresses food intake and body weight in mice. Journal of Biological Chemistry, 291(16), 8379–8386.

Gagne, S.J., Stout, J.M., Liu, E., Boubakir, Z., Clark, S.M., & Page, J.E. (2012). Identification of olivetolic acid cyclase from Cannabis sativa reveals a unique catalytic route to plant polyketides. Proceedings of the National Academy of Sciences, 109(31), 12811–12816.

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