Lead acetate basic - PbO：75.6~80.5 % , CAS No.51404-69-4

CAS: 51404-69-4 Cat. No.: L193681 Fórmula: C₄H₈O₆Pb₂ Peso molecular: 566.50 Número CE: 257-175-3

GRADE & PURITY PbO：75.6~80.5 %

Synonyms

AKOS030228727 | CCRIS 4042 | EC 257-175-3 | Lead(II) acetate basic, LR, anhydrous, 72-75% Pb basis, 21.5-24% acetic acid basis | Acetic acid, lead salt, basic | Lead(II) acetate basic | EINECS 257-175-3 | Lead(II) acetate basic, anhydrous, ACS reagent, fo

Storage

Room temperature,Argon charged

Shipped In

Normal

Visão geral

Lead acetate is a white crystalline solid, that is prepared by dissolving lead (II) oxide or lead (II) carbonate in concentrate d acetic acid. It is very soluble in water and its solution is often used to prepare other compounds. A trihydrate known as the “sugar of lead” because of its sweet taste, is the most common commercial form of lead (II) acetate, and can be prepared by dissolving lead (II) oxide in hot dilute acetic acid. It is generally used for dyeing and cloth printing, in the production of other lead compounds and of lead acetate

Specifications

Sinónimos

AKOS030228727 | CCRIS 4042 | EC 257-175-3 | Lead(II) acetate basic, LR, anhydrous, 72-75% Pb basis, 21.5-24% acetic acid basis | Acetic acid, lead salt, basic | Lead(II) acetate basic | EINECS 257-175-3 | Lead(II) acetate basic, anhydrous, ACS reagent, fo

Especificações e pureza

PbO：75.6~80.5 %

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Nomes e identificadores

• Pubchem Sid: 488201120
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488201120
• Sorrisos canónicos: CC(=O)O[Pb]OC(=O)C.O.O.[Pb]
• InChIKey: XAOPZCQFBUCRKR-UHFFFAOYSA-L
• INCHI: 1S/2C2H4O2.2H2O.2Pb/c2*1-2(3)4;;;;/h2*1H3,(H,3,4);2*1H2;;/q;;;;;+2/p-2
• SMILES isoméricas: CC(=O)O[Pb]OC(=O)C.O.O.[Pb]
• Peso molecular: 566.50

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Dicarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Dicarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Dicarboxylic acids and derivatives
• Alternative Parents: Acetate salts Organic oxoanionic compounds Organic oxides Organic lead salts Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dicarboxylic acid or derivatives - Acetate salt - Carboxylic acid salt - Organic metal salt - Organic plumbite - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic lead salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid 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

Propriedades químicas e físicas

• Sensibilidade: Air sensitive
• Peso molecular: 570.000 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 570.001 Da
• Monoisotopic Mass: 570.001 Da
• Topological Polar Surface Area: 54.600 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 110.000
• 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: 4

XLogP3

Referências

1. Qianfen Zhuang, Chao Zeng, Yaxin Mu, Tao Zhang, Guotao Yi, Yong Wang.  (2023)  Lead(II)-triggered aggregation-induced emission enhancement of adenosine-stabilized gold nanoclusters for enhancing photoluminescence detection of nabam—disodium ethylenebis(dithiocarbamate).  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.144113]

2. Congyang Mao, Wanyu Jin, Yiming Xiang, Yizhou Zhu, Jun Wu, Xiangmei Liu, Shuilin Wu, Wei Qiao, Kenneth M. C. Cheung, Kelvin Wai Kwok Yeung.  (2025)  Biosynthesis of H2S and Siderophores Targeting Gram-Negative Bacterial Resistance to Reactive Oxygen Species.  Advanced Science,      [PMID:40948366] [10.1002/advs.202505748]

Perguntas frequentes

How should this product be stored?

Store at room temperature under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 51404-69-4, the molecular formula is C4H8O6Pb2, and the molecular weight is 566.50 g/mol. InChIKey XAOPZCQFBUCRKR-UHFFFAOYSA-L.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.