Anhydrous lead acetate - ≥99% , CAS No.301-04-2

CAS: 301-04-2 Cat. No.: L196609 Formula: Pb(CH₃COO)₂ Peso molecolare: 325.29 Numero EC: 206-104-4

GRADE & PURITY ≥99%

Synonyms

Caswell No. 523A | Acetic acid, lead(2+) salt | EINECS 206-104-4 | Acetic acid, lead(II) salt | Lead(II) acetate | Bleiacetat [German] | Leadac | SCHEMBL56749 | Lead acetate anhydrous | Acetate de plomb | Acetic acid lead(2+) salt | LEAD ACETATE, ANHYDROU

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Panoramica

Lead Diacetate is a reagent used in hair colouring dyes. It is also used for enantioselective C-H olefination of diphenylacetic acids.

Specifications

Sinonimi

Caswell No. 523A | Acetic acid, lead(2+) salt | EINECS 206-104-4 | Acetic acid, lead(II) salt | Lead(II) acetate | Bleiacetat [German] | Leadac | SCHEMBL56749 | Lead acetate anhydrous | Acetate de plomb | Acetic acid lead(2+) salt | LEAD ACETATE, ANHYDROU

Specifiche e purezza

≥99%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

FedEx DG Service

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

504751821

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751821

Sorrisi canonici

CC(=O)[O-].CC(=O)[O-].[Pb+2]

IUPAC Name

lead(2+);diacetate

InChIKey

GUWSLQUAAYEZAF-UHFFFAOYSA-L

INCHI

1S/2C2H4O2.Pb/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

Isomeri SMILES

CC(=O)[O-].CC(=O)[O-].[Pb+2]

Numero UN

1616

Gruppo di imballaggio

III

Peso molecolare

325.29

Reaxy-Rn

3692537

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3692537&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: 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 oxides Organic lead salts 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 lead salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: 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: lead coordination entity

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

• Solubilità: DMSO (Slightly), Methanol (Slightly)
• Sensibilità: Moisture Sensitive
• Punto di fusione (°C): 280°C(lit.)
• Peso molecolare: 325.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 326.003 Da
• Monoisotopic Mass: 326.003 Da
• Topological Polar Surface Area: 80.300 Ų
• Heavy Atom Count: 9
• 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: 3

XLogP3