Potassium tartrate - GR , CAS No.921-53-9

CAS: 921-53-9 Cat. No.: P112435 Formula: C₄H₄O₆K₂ Peso molecolare: 226.27 Numero EC: 213-067-8

GRADE & PURITY GR

Synonyms

921-53-9|Dipotassium;2,3-dihydroxybutanedioate|potassium tartarate|Potassiumtartrate&nbs|SCHEMBL80796|AVTYONGGKAJVTE-UHFFFAOYSA-L|AKOS015836341|AS-81988

Storage

Room temperature

Shipped In

Normal

Specifications

Sinonimi

921-53-9 | Dipotassium;2,3-dihydroxybutanedioate | potassium tartarate | Potassiumtartrate&nbs | SCHEMBL80796 | AVTYONGGKAJVTE-UHFFFAOYSA-L | AKOS015836341 | AS-81988

Specifiche e purezza

GR

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Grado

GR

Nomi e identificatori

• Pubchem Sid: 508816729
• Sorrisi canonici: C(C(C(=O)[O-])O)(C(=O)[O-])O.[K+].[K+]
• IUPAC Name: dipotassium;2,3-dihydroxybutanedioate
• InChIKey: AVTYONGGKAJVTE-UHFFFAOYSA-L
• INCHI: 1S/C4H6O6.2K/c5-1(3(7)8)2(6)4(9)10;;/h1-2,5-6H,(H,7,8)(H,9,10);;/q;2*+1/p-2
• Isomeri SMILES: C(C(C(=O)[O-])O)(C(=O)[O-])O.[K+].[K+]
• Peso molecolare: 226.27
• Reaxy-Rn: 7838980
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7838980&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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 potassium 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 potassium salt - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organic salt - Organic cation - Aliphatic acyclic compound
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive.
• Peso molecolare: 226.270 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 225.928 Da
• Monoisotopic Mass: 225.928 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 123.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

Riferimenti

1. Yiqiong Liu, Dailin Xu, Ying Liu, Xiao Zheng, Jie Zang, Wanli Ye, Yuge Zhao, Ruiqing He, Shuangrong Ruan, Tingting Zhang, Haiqing Dong, Yan Li, Yongyong Li.  (2022)  Remotely boosting hyaluronidase activity to normalize the hypoxic immunosuppressive tumor microenvironment for photothermal immunotherapy.  BIOMATERIALS,      [PMID:35436740] [10.1016/j.biomaterials.2022.121516]

2. Mi Feng, Jipeng Yan, Bin He, Xinyan Chen, Jian Sun.  (2021)  Controllable conversion of shrimp shells into chitin or derived carbon material using acidic deep eutectic solvent.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:34695496] [10.1016/j.ijbiomac.2021.10.122]

3. Shanqi Guo, Yangyi Zhang, Shuo Wang, Tong Yang, Baojie Ma, Xiaojiang Li, Yizhuo Zhang, Xingkang Jiang.  (2021)  LncRNA PCA3 promotes antimony-induced lipid metabolic disorder in prostate cancer by targeting MIR-132-3 P/SREBP1 signaling.  TOXICOLOGY LETTERS,      [PMID:34052307] [10.1016/j.toxlet.2021.05.006]

4. Xiuzhen Zhu, Yuan Gao, Qinyan Yue, Yan Song, Baoyu Gao, Xing Xu.  (2018)  Facile synthesis of hierarchical porous carbon material by potassium tartrate activation for chloramphenicol removal.  Journal of the Taiwan Institute of Chemical Engineers,      [PMID:] [10.1016/j.jtice.2018.01.025]

5. Licheng Lin, Zhentao Li, Xi Song, Yanpeng Jiao, Changren Zhou.  (2018)  Preparation of chitosan/lanthanum hydroxide composite aerogel beads for higher phosphorus adsorption.  MATERIALS LETTERS,      [PMID:] [10.1016/j.matlet.2018.02.014]

6. Xiuzhen Zhu, Yuan Gao, Qinyan Yue, Yujiao Kan, Wenjia Kong, Baoyu Gao.  (2017)  Preparation of green alga-based activated carbon with lower impregnation ratio and less activation time by potassium tartrate for adsorption of chloramphenicol.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:28755646] [10.1016/j.ecoenv.2017.07.053]

7. Hongmei Luo, Lichao Jiang, Yuxin Guo, Min Li, Longyu Hu, Hao Wu, Wei Cui, Rong Ran.  (2024)  Extreme Toughening of Conductive Hydrogels Through Synergistic Effects of Mineralization, Salting-Out, and Ion Coordination Induced by Multivalent Anions.  Small,      [PMID:39575504] [10.1002/smll.202409565]

8. Hengzhuo Cai, Junfeng Lin, Wanyang Lyu, Lingyi Yi, Xubing Lu, Xingsen Gao, Jun-Ming Liu, Sujuan Wu.  (2026)  Performance Enhancement of All-Inorganic CsPbI3 Perovskite Solar Cells through Functional Additive and Buried Interface Engineering.  Small,      [PMID:42464936] [10.1002/smll.74390]