Bismuth(III) acetate - ≥99.9% metals basis , CAS No.22306-37-2

CAS: 22306-37-2 Cat. No.: B303105 Peso molecular: 386.11 Número EC: 244-904-5

GRADE & PURITY ≥99.9% metals basis

Synonyms

DTXSID101043458 | EINECS 249-426-0 | WKLWZEWIYUTZNJ-UHFFFAOYSA-K | D70195 | AKOS015915836 | C6H9BiO6 | FT-0725987 | bismuth(iii)acetate | 8AJA86Y692 | NSC 370498 | Acetic acid, bismuth salt | EINECS 244-904-5 | bismuth;triacetate | UNII-8AJA86Y692 | BISMU

Storage

Room temperature,Argon charged

Shipped In

Normal

Descripción general

(1) Bismuth (III) acetate is used as a raw material for the synthesis of bismuth (III) sulfide (Bi2S3), which can be used in solution-processable bulk heterojunction solar cells.

(2) Used to prepare gold-bismuth sulfide (Au-Bi2S3) heterogeneous nanostructures and bismuth titanate nanorods [4] as photocatalysts.

(3) It is also used to synthesize triarylbismuth compounds.

Specifications

Sinónimos

DTXSID101043458 | EINECS 249-426-0 | WKLWZEWIYUTZNJ-UHFFFAOYSA-K | D70195 | AKOS015915836 | C6H9BiO6 | FT-0725987 | bismuth(iii)acetate | 8AJA86Y692 | NSC 370498 | Acetic acid, bismuth salt | EINECS 244-904-5 | bismuth;triacetate | UNII-8AJA86Y692 | BISMU

Especificaciones y pureza

≥99.9% metals basis

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥99.9% metals basis

Nombres e identificadores

• Pubchem Sid: 504753423
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753423
• Sonrisas canónicas: CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Bi+3]
• IUPAC Name: bismuth;triacetate
• InChIKey: WKLWZEWIYUTZNJ-UHFFFAOYSA-K
• INCHI: 1S/3C2H4O2.Bi/c3*1-2(3)4;/h3*1H3,(H,3,4);/q;;;+3/p-3
• Isómeros SMILES: CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Bi+3]
• Peso molecular: 386.11
• Reaxy-Rn: 5428753
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5428753&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid salts
          • Level6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Monocarboxylic acids and derivatives Carboxylic acids Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Acetate salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• 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

• Sensibilidad: Moisture sensitive
• Peso molecular: 386.110 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 386.02 Da
• Monoisotopic Mass: 386.02 Da
• Topological Polar Surface Area: 120.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 25.500
• 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: 4

XLogP3

Referencias

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