Sodium Dichloroacetate - Moligand™, 10mM in DMSO , Pyruvate dehydrogenase kinase inhibitor, CAS No.2156-56-1, Pyruvate dehydrogenase kinase inhibitor

CAS: 2156-56-1 Cat. No.: S422596 Molecular Weight: 150.92 Beilstein Registry Number: 2(2)194 EC Number: 218-461-3 PubChem CID: 517326
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
Sodium dichloroacetate|2156-56-1|sodium 2,2-dichloroacetate|Dichloroacetic acid sodium salt|Ceresine|Dichloroacetate Sodium|ACETIC ACID, DICHLORO-, SODIUM SALT|Dca sodium|CPC-211|DCA|Sodium dichloroacetate [USAN]|Bichloroacetic Acid|SodiumDichloroacetate-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1ml
S422596-1ml
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Why this grade

Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Sodium dichloroacetate is a mitochondrial pyruvate dehydrogenase kinase (PDK) inhibitor that exhibits potent anti-leukemic activity.

Sodium dichloroacetate can be used as an organic salt precursor for synthesizing microporous carbon that is useful in developing carbon-based adsorbents.

Specifications

Synonyms
Sodium dichloroacetate | 2156-56-1 | sodium 2, 2-dichloroacetate | Dichloroacetic acid sodium salt | Ceresine | Dichloroacetate Sodium | ACETIC ACID, DICHLORO-, SODIUM SALT | Dca sodium | CPC-211 | DCA | Sodium dichloroacetate [USAN] | Bichloroacetic Acid | SodiumDichloroacetate-
Specifications & Purity
Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms
Inhibitor of mitochondrial pyruvate dehydrogenase kinase (PDK). Shifts pyruvate metabolism from glycolysis and lactate production to glucose oxidation in the mitochondria. Induces mitochondrial-dependent apoptosis and reverses the inhibition/downregulatio
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
INHIBITOR
Mechanism of action
Pyruvate dehydrogenase kinase inhibitor
Names and Identifiers
Canonical SmilesC(C(=O)[O-])(Cl)Cl.[Na+]
IUPAC Namesodium;2,2-dichloroacetate
InChIKeyLUPNKHXLFSSUGS-UHFFFAOYSA-M
INCHI1S/C2H2Cl2O2.Na/c3-1(4)2(5)6;/h1H,(H,5,6);/q;+1/p-1
Isomeric SMILES C(C(=O)[O-])(Cl)Cl.[Na+]
WGK Germany 2
RTECS AG9275000
PubChem CID 517326
Molecular Weight 150.92
Beilstein 2(2)194
Reaxy-Rn 3916178

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAlpha-halocarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAlpha-halocarboxylic acids
Alternative Parents Carboxylic acid salts  Organic metal halides  Monocarboxylic acids and derivatives  Carboxylic acids  Organochlorides  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl chlorides  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha-halocarboxylic acid - Carboxylic acid salt - Organic metal halide - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Alkyl chloride - Organic salt - Organooxygen compound - Organochloride - Organohalogen compound - Organic sodium salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alkyl halide - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha-halocarboxylic acids. These are carboxylic acids containing a halogen atom bonded to the alpha carbon atom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ROCK2 Tclin Rho-associated protein kinase 2 (6206 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDK1 Tchem Pyruvate dehydrogenase kinase isoform 1 (2021 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A-375 (9258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BGC-823 (3035 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1975 (4994 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bel-7402 (4577 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KB (17409 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1650 (1118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CISD1 Tchem CDGSH iron-sulfur domain-containing protein 1 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCD-841CoN (99 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
4T1 (1737 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pdk1 Pyruvate dehydrogenase kinase (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SensitivityMoisture sensitive.
Melt Point(°C)198 °C
Molecular Weight150.920 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass149.925 Da
Monoisotopic Mass149.925 Da
Topological Polar Surface Area40.100 Ų
Heavy Atom Count7
Formal Charge0
Complexity64.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Documents & Articles
Citations of This Product
References
1. Ziyuan Huang, Liangfeng Huang, Yanjuan Huang, Yuanfeng He, Xiaoqi Sun, Xiang Fu, Xiaoyu Xu, Gaofei Wei, Dawei Chen, Chunshun Zhao.  (2017)  Phthalocyanine-based coordination polymer nanoparticles for enhanced photodynamic therapy.  Nanoscale,  (41): (15883-15894).  [PMID:28994841] [10.1039/C7NR05402E]
2. Shengcun Ma, Xiaoqi Guo, Baiyang Chen.  (2016)  Toward better understanding of chloral hydrate stability in water: Kinetics, pathways, and influencing factors.  CHEMOSPHERE,      [PMID:27206269] [10.1016/j.chemosphere.2016.05.018]
3. Shiyuan Xiao, Yue Li, Jun Wang, Mengran Wang, Bing Bu, Wenmin Jiang.  (2025)  Lactylated histone H4K8 regulation of MFN2/Wnt signaling integrates glycolytic metabolism and Müller cell activation in the pathogenesis of glaucoma.  NEUROBIOLOGY OF DISEASE,      [PMID:41197676] [10.1016/j.nbd.2025.107178]
4. Xinyu Zhang, Yujie Liu, Ziling Yuan, Haomin Chen, Danyang Ma, Bingzhi Li, Ruihua Liu, Chao Yang.  (2025)  Metabolic engineering of Pseudomonas putida for mineralization of 1,2-dichloroethane and 2,4-dichlorophenoxyacetic acid and its application in wastewater bioremediation.  Journal of Environmental Chemical Engineering,  14  (1): (120844).  [PMID:] [10.1016/j.jece.2025.120844]
5. Ye Tian, Mengxing Yu, Lei Wang, Xiaohan Zhu, Jiahui Wei, Ningbo Yang, Fengli Yu, Bing Yuan.  (2026)  Highly dispersed copper on lignin-based nitrogen-doped mesoporous carbon for selective hydrodeoxygenation of vanillin.  Journal of Environmental Chemical Engineering,  14  (3): (122304).  [PMID:] [10.1016/j.jece.2026.122304]
Solution Calculators
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