Lead(IV) acetate - ≥96%, Contains 4-10% Glacial Acetic acid , CAS No.546-67-8

CAS: 546-67-8 Cat. No.: L106809 Molecular Weight: 443.38 Beilstein Registry Number: 3595640 EC Number: 208-908-0 PubChem CID: 9846230

GRADE & PURITY ≥96%, Contains 4-10% Glacial Acetic acid

Synonyms

LTA | lead (IV) tetra acetate | lead tetra-acetate | Lead tetracetate | Lead (IV) Acetate | Tetrakis(acetato-kappaO,kappaO')lead | AKOS025243798 | DTXSID801047756 | Lead (IV) Aceate | Lead (IV) tetraacetate | lead (IV) tetra-acetate | C8H12O8Pb | L0021

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

LTA | lead (IV) tetra acetate | lead tetra-acetate | Lead tetracetate | Lead (IV) Acetate | Tetrakis(acetato-kappaO, kappaO')lead | AKOS025243798 | DTXSID801047756 | Lead (IV) Aceate | Lead (IV) tetraacetate | lead (IV) tetra-acetate | C8H12O8Pb | L0021

Specifications & Purity

≥96%, Contains 4-10% Glacial Acetic acid

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥96%

Names and Identifiers

• Canonical Smiles: CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Pb]
• InChIKey: NVTAREBLATURGT-UHFFFAOYSA-J
• INCHI: 1S/4C2H4O2.Pb/c4*1-2(3)4;/h4*1H3,(H,3,4);/p-4
• Isomeric SMILES: CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Pb]
• WGK Germany: 3
• RTECS: AI5300000
• PubChem CID: 9846230
• UN Number: 2291
• Packing Group: III
• Molecular Weight: 443.38
• Beilstein: 3595640
• Reaxy-Rn: 3595640

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Organic lead salts Hydrocarbon derivatives Carbonyl compounds Organic anions
• Molecular Framework: Not available
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic lead salt - Organic salt - Organooxygen compound - Carbonyl group - Organic anion - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• 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

Chemical and Physical Properties

• Solubility: Soluble in water, ethanol, chloroform, benzene, nitrobenzene, tetrachloroethane, nitric acid, hot acetic acid and hydrochloric acid.
• Sensitivity: Moisture sensitive;air sensitive;heat sensitive
• Melt Point(°C): 175°C
• Molecular Weight: 443.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 0
• Exact Mass: 444.03 Da
• Monoisotopic Mass: 444.03 Da
• Topological Polar Surface Area: 161.000 Ų
• Heavy Atom Count: 17
• Formal Charge: -4
• 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: 5

XLogP3

References

1. Yanyue Liu, Yisheng Sun, Mengting Ye, Liqin Zhu, Lili Zhang, Shuhua Zhu.  (2021)  Improvement in storage quality of postharvest tomato fruits by nitroxyl liposomes treatment.  FOOD CHEMISTRY,      [PMID:33951606] [10.1016/j.foodchem.2021.129933]