Bismuth(III) citrate - PrimorTrace™, ≥99.99% metals basis , CAS No.813-93-4

CAS: 813-93-4 Cat. No.: B475200 Peso molecular: 398.08 Número EC: 212-390-1

GRADE & PURITY PrimorTrace™, ≥99.99% metals basis

Synonyms

BISMUTH CITRATE

Storage

Protected from light,Room temperature

Shipped In

Normal

Descripción general

Description

Bismuth(III) citrate has been used as a sorbent in spin columns to develop a novel stationary phase for the selective and efficient isolation of phenolic compounds from natural sources via solid phase extraction (SPE) method. It can be used to synthesize bismuth subcarbonate ((BiO)2CO3) nanotubes that are reported to show antibacterial property againstHelicobacter pylori.

Specifications

Sinónimos

BISMUTH CITRATE

Especificaciones y pureza

PrimorTrace™, ≥99.99% metals basis

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Grado

PrimorTrace™

Pureza

≥99.99% metals basis

Nombres e identificadores

• Pubchem Sid: 504752424
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752424
• Sonrisas canónicas: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Bi+3]
• IUPAC Name: bismuth;2-hydroxypropane-1,2,3-tricarboxylate
• InChIKey: ANERHPOLUMFRDC-UHFFFAOYSA-K
• INCHI: 1S/C6H8O7.Bi/c7-3(8)1-6(13,5(11)12)2-4(9)10;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);/q;+3/p-3
• Isómeros SMILES: C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Bi+3]
• Peso molecular: 398.08
• Reaxy-Rn: 11330266
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11330266&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Tricarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Tricarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Tricarboxylic acids and derivatives
• Alternative Parents: Tertiary alcohols Carboxylic acid salts Carboxylic acids Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tricarboxylic acid or derivatives - Tertiary alcohol - Carboxylic acid salt - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.
• 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

Propiedades químicas y físicas

• Solubilidad: nsoluble in water, alcohol, ether. Soluble in ammonia solution and in solution of alkali citrates；Soluble in ammonia, alkali citrates. Insoluble in water, alcohol and ether.
• Sensibilidad: light sensitive
• Punto de fusión (°C): 300 °C
• Peso molecular: 398.080 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 397.984 Da
• Monoisotopic Mass: 397.984 Da
• Topological Polar Surface Area: 141.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 211.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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