Sodium tartrate dibasic dihydrate - AR, ≥99% , CAS No.6106-24-7

CAS: 6106-24-7 Cat. No.: S111691 Molecular Weight: 230.08 Beilstein Registry Number: 6121732 EC Number: 612-074-7

GRADE & PURITY AR, ≥99%

Synonyms

DTXSID20976556 | HMS1922I06 | EINECS 244-643-7 | Sodium tartrate dibasic dihydrate, BioXtra, >=99.0% | Pharmakon1600-01503262 | Sodium L-(+)-Tartaric Acid Dihydrate | Sodium Tartrate Dihydrate, Pharmaceutical Secondary Standard; Certified Reference Materi

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

DTXSID20976556 | HMS1922I06 | EINECS 244-643-7 | Sodium tartrate dibasic dihydrate, BioXtra, >=99.0% | Pharmakon1600-01503262 | Sodium L-(+)-Tartaric Acid Dihydrate | Sodium Tartrate Dihydrate, Pharmaceutical Secondary Standard; Certified Reference Materi

Specifications & Purity

AR, ≥99%

Storage

Room temperature

Shipped In

Normal

Grade

AR

Purity

≥99%

Names and Identifiers

• Pubchem Sid: 488198170
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198170
• Canonical Smiles: C(C(C(=O)[O-])O)(C(=O)[O-])O.O.O.[Na+].[Na+]
• IUPAC Name: disodium;(2R,3R)-2,3-dihydroxybutanedioate;dihydrate
• InChIKey: FGJLAJMGHXGFDE-DGFHWNFOSA-L
• INCHI: 1S/C4H6O6.2Na.2H2O/c5-1(3(7)8)2(6)4(9)10;;;;/h1-2,5-6H,(H,7,8)(H,9,10);;;2*1H2/q;2*+1;;/p-2/t1-,2-;;;;/m1..../s1
• Isomeric SMILES: [C@@H]([C@H](C(=O)[O-])O)(C(=O)[O-])O.O.O.[Na+].[Na+]
• WGK Germany: 3
• Molecular Weight: 230.08
• Beilstein: 6121732
• Reaxy-Rn: 16926950
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=16926950&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Hydroxy acids and derivatives
      • Subclass Beta hydroxy acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Hydroxy acids and derivatives
• Subclass: Beta hydroxy acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Beta hydroxy acids and derivatives
• Alternative Parents: Short-chain hydroxy acids and derivatives Monosaccharides Fatty acids and conjugates Dicarboxylic acids and derivatives Secondary alcohols Carboxylic acid salts 1,2-diols Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Short-chain hydroxy acid - Dicarboxylic acid or derivatives - Monosaccharide - Fatty acid - 1,2-diol - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Organic alkali metal salt - Organic sodium salt - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organic salt - Organic cation - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Moisture sensitive.
• Specific Rotation[α]: 26 ° (C=5, H2O)
• Molecular Weight: 230.080 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 1
• Exact Mass: 230.001 Da
• Monoisotopic Mass: 230.001 Da
• Topological Polar Surface Area: 123.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 123.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 5

XLogP3

References

1. Weiying Wang, Jiayao Wang, Jingguo Li, Shaokui Cao, Jun Shi.  (2023)  In situ growth of MoS2@AuNRs nanoparticles with synergistically enhanced NIR response for controlled drug release.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2023.107448]

2. Ruican Wang, Richard W. Hartel, Jing Wu, Qisijing Liu, Jin Wang, Shuo Wang.  (2023)  Phase separation phenomena in gelatin-glucose syrup mixtures: Microstructures and gel characterization.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2023.109378]

3. Qinghai Long, Shuo Wang, Shufeng Shen.  (2023)  CO2 capture using EGHE-based water-lean solvents with novel water balance design.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2023.118658]

4. Bu Jun, Liu Zhenpeng, Ma Wenxiu, Zhang Lei, Wang Tao, Zhang Hepeng, Zhang Qiuyu, Feng Xinliang, Zhang Jian.  (2021)  Selective electrocatalytic semihydrogenation of acetylene impurities for the production of polymer-grade ethylene.  Nature Catalysis,  4  (7): (557-564).  [PMID:] [10.1038/s41929-021-00641-x]

5. Yuanjie Teng, Zeyu Ren, Yuchao Zhang, Zhenni Wang, Zaifa Pan, Kang Shao, Yuanbin She.  (2019)  Fabrication of liquid–liquid self-assembled Ag arrays on disposable screen-printed electrodes and their application in the identification and analysis of the adsorption behavior of organic carboxylates through in situ electrochemical surface-enhanced Raman scattering.  NEW JOURNAL OF CHEMISTRY,  44  (5): (1777-1784).  [PMID:] [10.1039/C9NJ06000F]

6. Xinxin Han, Enhai Song, Bo Zhou, Qinyuan Zhang.  (2019)  Color tunable upconversion luminescent perovskite fluoride with long-/short-lived emissions toward multiple anti-counterfeiting.  Journal of Materials Chemistry C,  7  (27): (8226-8235).  [PMID:] [10.1039/C9TC02171J]

7. Yuhua Yan, Yanping Tian, Meifeng Hao, Yuqing Miao.  (2016)  Synthesis and characterization of cross-like Ni-Co-P microcomposites.  MATERIALS & DESIGN,      [PMID:] [10.1016/j.matdes.2016.08.094]

8. Jing Gao, Li Chen, Zongcheng Yan.  (2015)  Phase Behavior of Aqueous Biphasic Systems Composed of Ionic Liquids and Organic Salts.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/je500419b]

9. Donghui Han, Jinquan Wan, Yongwen Ma, Yan Wang, Ying Li, Dongya Li, Zeyu Guan.  (2015)  New insights into the role of organic chelating agents in Fe(II) activated persulfate processes.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2015.01.106]

10. Zhixuan Ma, Jing Wang, Shufeng Shen.  (2024)  Development of novel amino acid salt-based liquid-liquid-solid absorbent for energy-efficient post-combustion CO2 capture.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.128970]

11. Menglu An, Weiying Wang, Jingguo Li, Shaokui Cao, Yingliang Liu, Jun Shi.  (2025)  MoS2@AuNRs nanoparticles equipped with MnO2 nanosheets as an efficient NIR/pH/GSH triple-responsive drug delivery carrier.  POWDER TECHNOLOGY,      [PMID:] [10.1016/j.powtec.2025.120941]

12. Maojiang Zhang, Kexin Cui, Xinwei Zhang, Jinghua Wang, Minglei Wang, Yanfu Wu, Chunlei Dong, Jie Gan, Jiangtao Hu, Guozhong Wu.  (2024)  Ultraviolet curing technology plus chemical copper plating: A novel method for producing highly durable fabric-based flexible circuit.  POLYMERS FOR ADVANCED TECHNOLOGIES,  35  (9): (e6563).  [PMID:] [10.1002/pat.6563]

13. Xiaoxue Zhang, Niu Liu, Zhen-Feng Huang, Ru Jia, Lun Pan, Chengxiang Shi, Xiangwen Zhang, Guidong Yang, Ji-Jun Zou.  (2026)  Tip-Enhanced Electric Fields on Dendritic Copper Accelerate Water Dissociation for Selective Nitrate-To-Ammonia Electroreduction.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.6c01209]