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

CAS: 301-04-2 Cat. No.: L196609 Summenformel: Pb(CH₃COO)₂ Molekulargewicht: 325.29 EG-Nummer: 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

Übersicht

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

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥99%

Storage

Room temperature,Argon charged

Verschickt in

FedEx DG Service

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

504751821

Pubchem Sid Url

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

Kanonisches Lächeln

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

Isomere SMILES

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

UN-Nummer

1616

Verpackungsgruppe

III

Molekulargewicht

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
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Ebene5 Carboxylic acid salts
          • Ebene6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: DMSO (Slightly), Methanol (Slightly)
• Empfindlichkeit: Moisture Sensitive
• Schmelzpunkt (°C): 280°C(lit.)
• Molekulargewicht: 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