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CAS 15187-16-3

Lead(II) Phthalocyanine (purified by sublimation) TCI L0230

Lead(II) Phthalocyanine (purified by sublimation) TCI L0230

Chemical Identity

CAS No.
15187-16-3
PubChem
CID 167255·SID 253659752
Formula
C32H16N8Pb
Molecular weight
720 g/mol
Purity
>98.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2,11,20,29,37,39-hexaza-38,40-diazanidanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13,15,17,19(39),20,22,24,26,28,30(37),31,33,35-nonadecaene;lead(2+)
SMILES
C1=CC=C2C(=C1)C3=NC4=NC(=NC5=C6C=CC=CC6=C([N-]5)N=C7C8=CC=CC=C8C(=N7)N=C2[N-]3)C9=CC=CC=C94.[Pb+2]
InChIKey
WSQYJDCCFQPFJC-UHFFFAOYSA-N
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Lead(II) Phthalocyanine is a chemical compound belonging to the class of metal complexes, widely utilized in the fields of catalysis and inorganic chemistry. It is a synthetic compound known for its unique molecular structure and intense coloration, typically appearing as a deep blue or blue-green hue. In laboratory settings, this compound plays a crucial role as a catalyst in various chemical reactions, particularly in oxidation and reduction processes. Its ability to stabilize and facilitate complex chemical transformations makes it an essential component in both academic and industrial research environments.

One of the key properties that make Lead(II) Phthalocyanine a preferred choice is its exceptional chemical and thermal stability. It exhibits high resistance to degradation when exposed to organic solvents, ensuring consistent performance in prolonged experimental conditions. Additionally, its ability to form stable complexes with various ligands enhances its utility in catalytic systems. The compound's high purity, achieved through sublimation purification, ensures that it meets the stringent quality requirements of advanced scientific research.

In Indonesian laboratories, Lead(II) Phthalocyanine is commonly used in chemical synthesis and material development experiments. Its reliability and performance in catalytic applications make it a favored material for researchers working on inorganic chemistry and advanced chemical processes. Its versatility and high-quality standards support its widespread use in both academic and industrial research settings.

TCI brochures (PDF)

  • Catalytic Oxidation Reactions: Lead(II) Phthalocyanine is ideal for oxidation processes due to its stability and ability to facilitate electron transfer.
  • Reduction Processes in Organic Chemistry: Its unique electronic structure makes it effective in promoting reduction reactions in organic synthesis.
  • Material Science Research: The compound is used in the development of new materials due to its structural and optical properties.
  • Inorganic Chemistry Experiments: Its role as a metal complex makes it a valuable tool for studying coordination chemistry and metal-ligand interactions.
  • Analytical Chemistry Applications: Its intense coloration aids in spectroscopic analysis and qualitative testing in laboratory settings.

Brand TCI
CAS number 15187-16-3
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Main-group Elements [Catalysis and Inorganic Chemistry]
Pack sizes As per supplier specifications
Physical form Powder
Storage Store in a cool, dry place away from light and moisture

Lead(II) Phthalocyanine should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep the compound in a sealed container to prevent exposure to air and contaminants. Due to its chemical stability, it does not require refrigeration but should be protected from prolonged exposure to humidity. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is not highly toxic, it is advisable to avoid inhalation of dust and ensure proper ventilation during handling. The compound is generally stable under normal storage conditions, making it suitable for long-term use in research applications.

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