Bismuth(III) citrate - PrimorTrace™, ≥99.9% metals basis , CAS No.813-93-4

CAS: 813-93-4 Cat. No.: B776936 Formule: C₆H₅BiO₇ Poids moléculaire: 398.08 Numéro CE: 212-390-1

QUALITÉ & PURETÉ PrimorTrace™, ≥99.9% metals basis

Synonyms

Bismuth citrate

Storage

Protected from light,Room temperature

Shipped In

Normal

Vue d’ensemble

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.

Spécifications

Synonymes

Bismuth citrate

Spécifications et pureté

PrimorTrace™, ≥99.9% metals basis

Conditions de stockage de stockage

Protected from light,Room temperature

Expédié en

Normal

Grade

PrimorTrace™

Pureté

≥99.9% metals basis

Noms et identifiants

Pubchem Sid

528772190

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528772190

Sourires canoniques

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

Isomères SMILES

C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O.[Bi+3]

Poids moléculaire

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
    • Classe Carboxylic acids and derivatives
      • Subclass Tricarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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
• Description: 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

Propriétés chimiques et physiques

• Solubilité: 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.
• Sensibilité: light sensitive
• Point de fusion (°C): 300 °C
• Poids moléculaire: 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