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Sodium dichloroacetate
[CAS# 2156-56-1]

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Identification
ClassificationOrganic raw materials >> Organometallic salt
NameSodium dichloroacetate
SynonymsDichloroacetic acid sodium salt
Molecular StructureCAS # 2156-56-1, Sodium dichloroacetate
Molecular FormulaC2HCl2NaO2
Molecular Weight150.92
CAS Registry Number2156-56-1
EC Number218-461-3
SMILESC(C(=O)[O-])(Cl)Cl.[Na+]
Properties
Melting point198 °C (Decomposes) (Expl.)
SolubilitySoluble 100 mM (water), 100 mM (DMSO) (Expl.)
Safety Data
Hazard Symbolssymbol symbol   GHS07;GHS08 Warning  Details
Risk StatementsH315-H319-H335-H351  Details
Safety StatementsP203-P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P318-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
CarcinogenicityCarc.2H351
Reproductive toxicityRepr.2H361
SDSAvailable
up Discovery and Applications
Sodium dichloroacetate is the sodium salt of dichloroacetic acid, a small halogenated carboxylate that has been studied extensively for its biochemical and pharmacological properties. The compound consists of a dichloromethyl group attached to a carboxylate anion, balanced by a sodium cation. Its scientific importance lies primarily in its role as a metabolic modulator and as a tool compound in studies of mitochondrial function and intermediary metabolism.

The discovery of dichloroacetic acid dates back to nineteenth-century investigations into chlorinated acetic acids, which were prepared during systematic explorations of halogen substitution reactions in simple organic acids. As methods for chlorination and purification improved, dichloroacetic acid and its salts, including sodium dichloroacetate, became well-defined chemical entities. Early interest centered on their chemical properties, acidity, and reactivity, which were compared with those of mono- and trichloroacetic acids to understand the effects of halogen substitution on carboxylic acids.

Sodium dichloroacetate later gained attention in biological and medical research due to its influence on cellular metabolism. In the mid-twentieth century, researchers studying carbohydrate metabolism identified dichloroacetate as an inhibitor of pyruvate dehydrogenase kinase. This inhibition leads to activation of the pyruvate dehydrogenase complex, promoting the conversion of pyruvate to acetyl-CoA and enhancing mitochondrial oxidation of glucose-derived carbon. The sodium salt form was favored in experimental work because of its high water solubility and ease of administration in aqueous systems.

The application of sodium dichloroacetate as a research tool expanded as interest grew in metabolic regulation and mitochondrial dysfunction. It has been widely used in laboratory studies to probe the balance between glycolysis and oxidative phosphorylation. By shifting cellular metabolism toward increased mitochondrial activity, sodium dichloroacetate has helped elucidate mechanisms underlying metabolic diseases, ischemia, and altered energy metabolism in various cell types. Its effects have been studied in isolated mitochondria, cultured cells, and animal models to better understand metabolic control points.

In addition to its role in metabolism research, sodium dichloroacetate has been investigated for potential therapeutic applications. Its ability to modify metabolic pathways prompted studies in conditions associated with impaired mitochondrial function or abnormal glucose metabolism. These investigations have primarily been conducted in experimental and clinical research settings, where the compound served as a pharmacological probe to test hypotheses about disease mechanisms rather than as an established treatment. Through this work, sodium dichloroacetate contributed to a broader appreciation of metabolism as a target for therapeutic intervention.

From a chemical and industrial perspective, sodium dichloroacetate has also been used as an intermediate and reagent. Dichloroacetate salts have found applications in organic synthesis, particularly in reactions where controlled acidity or the presence of a halogenated carboxylate is advantageous. In environmental and analytical chemistry, dichloroacetate has been studied as a byproduct of water chlorination processes, making sodium dichloroacetate relevant to investigations of water treatment and disinfection byproducts.

Safety and toxicological studies have accompanied the increased use of sodium dichloroacetate in research. These studies have examined its metabolism, distribution, and potential adverse effects, providing important context for its handling and experimental use. Such evaluations have reinforced the need for controlled dosing and careful interpretation of results when the compound is used in biological systems.

In summary, sodium dichloroacetate is a chemically simple yet biologically influential compound whose significance arises from its ability to modulate key metabolic pathways. From its origins in classical organic chemistry to its applications in modern metabolic research, it has served as an important tool for understanding mitochondrial function and energy metabolism. Its continued use reflects the enduring value of small, well-characterized molecules in advancing biochemical and physiological knowledge.

References

2025. Myocardial pyruvate dehydrogenase kinase 4 drives sex-specific cardiac responses to endotoxemia. JCI Insight.
DOI: 10.1172/jci.insight.191649

2025. 1,8-naphthalimide-based DNA intercalators and anticancer agents: a systematic review. Molecular Diversity.
DOI: 10.1007/s11030-025-11251-1
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