Potassium D-erythronate - ≥98% , CAS No.88759-55-1

CAS: 88759-55-1 Cat. No.: P344339 Molecular Weight: 174.19 EC Number: 857-708-5 PubChem CID: 23698876

GRADE & PURITY ≥98%

Synonyms

P20477 | Potassium(2R,3R)-2,3,4-trihydroxybutanoate | AKOS006275428 | HY-113048A | potassium;(2R,3R)-2,3,4-trihydroxybutanoate | EN300-263540 | AS-10638 | POTASSIUM D-ERYTHRONATE | DTXSID501344767 | Erythronic acid (potassium) | Potassium (2R,3R)-2,3,4-tr

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

P20477 | Potassium(2R, 3R)-2, 3, 4-trihydroxybutanoate | AKOS006275428 | HY-113048A | potassium;(2R, 3R)-2, 3, 4-trihydroxybutanoate | EN300-263540 | AS-10638 | POTASSIUM D-ERYTHRONATE | DTXSID501344767 | Erythronic acid (potassium) | Potassium (2R, 3R)-2, 3, 4-tr

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488200582
• Canonical Smiles: C(C(C(C(=O)[O-])O)O)O.[K+]
• IUPAC Name: potassium;(2R,3R)-2,3,4-trihydroxybutanoate
• InChIKey: NIBJBHRBFKKLFG-SWLXLVAMSA-M
• INCHI: 1S/C4H8O5.K/c5-1-2(6)3(7)4(8)9;/h2-3,5-7H,1H2,(H,8,9);/q;+1/p-1/t2-,3-;/m1./s1
• Isomeric SMILES: C([C@H]([C@H](C(=O)[O-])O)O)O.[K+]
• PubChem CID: 23698876
• Molecular Weight: 174.19

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar acids and derivatives
• Alternative Parents: Short-chain hydroxy acids and derivatives Beta hydroxy acids and derivatives Monosaccharides Fatty acids and conjugates Secondary alcohols Carboxylic acid salts 1,2-diols Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic zwitterions Organic potassium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Sugar acid - Short-chain hydroxy acid - Hydroxy acid - Fatty acid - Monosaccharide - 1,2-diol - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Organic alkali metal salt - Carboxylic acid - Monocarboxylic acid or derivatives - Polyol - Organic potassium salt - Alcohol - Organic oxide - Hydrocarbon derivative - Organic salt - Carbonyl group - Primary alcohol - Organic zwitterion - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
• 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

• Molecular Weight: 174.190 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 173.993 Da
• Monoisotopic Mass: 173.993 Da
• Topological Polar Surface Area: 101.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 106.000
• 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: 2

XLogP3

References

1. Baoyan Ding, Wei Meng, Xiaoling Zang, Zhihua Lv.  (2024)  Metabolic characteristics of prostate cancer cells with high metastatic potential revealed by (S)-ethyl 1-(3-(4-chlorophenoxy)-2-hydroxypropyl)-3-(4-methoxyphenyl)-1H-pyrazole-5-carboxylate inhibition.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:39662125] [10.1016/j.jpba.2024.116611]

2. Kui Zou, Hongbo Zhao.  (2025)  Ligand-induced tetrad effect in coordination leaching of ion-adsorption rare earth ores: enhanced recovery of high-value low-lanthanum rare earth concentrates.  GREEN CHEMISTRY,  27  (27): (8174-8187).  [PMID:] [10.1039/D5GC02367J]