Iron(III) Tetraphenylporphyrin Chloride TCI I0937

Chemical Identity

CAS No.: 16456-81-8
PubChem: CID 11643338·SID 468592055
Formula: C44H28ClFeN4
Molecular weight: 704.0 g/mol
Purity: >97.0%(T)(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: iron(3+);5,10,15,20-tetraphenyl-2H-porphyrin-2,15-diide;chloride
SMILES: [CH-]1C=C2C(=C3C=CC(=N3)C(=C4C=CC(=N4)[C-](C5=NC(=C(C1=N2)C6=CC=CC=C6)C=C5)C7=CC=CC=C7)C8=CC=CC=C8)C9=CC=CC=C9.[Cl-].[Fe+3]
InChIKey: ZDYSAMCSFRQDMN-UHFFFAOYSA-M

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Iron(III) Tetraphenylporphyrin Chloride is a chemical compound widely utilized in laboratory settings for catalytic reactions and C-H activation studies. As a member of the porphyrin family, it possesses a complex molecular structure that enables it to act as a highly reactive catalyst. This compound is particularly valuable in organic and inorganic chemistry research due to its ability to facilitate a variety of chemical transformations. Its unique electronic properties make it a versatile tool for scientists aiming to explore new reaction pathways and mechanisms.

The compound’s reactivity, stability, and solubility in organic solvents make it a preferred choice for many researchers. Its ability to maintain structural integrity under various experimental conditions ensures consistent performance in laboratory applications. Additionally, its high purity and predictable behavior contribute to reliable results in chemical experiments. These properties position Iron(III) Tetraphenylporphyrin Chloride as a key reagent in modern chemical research, especially in catalytic processes that require precise control over reaction conditions.

In Indonesian laboratories, Iron(III) Tetraphenylporphyrin Chloride is commonly used in chemical research, particularly in catalysis and C-H activation studies. Its availability and performance make it a popular choice among researchers working on organic and inorganic chemistry projects. Its use is especially prevalent in academic and industrial research settings where efficient and reliable catalytic systems are required. The compound’s role in advancing chemical innovation is well recognized in the scientific community.

TCI brochures (PDF)

Hydrosilane for Alkene Hydrogenation and Quaternary Carbon Construction through C–C Bond Formation 2025-09-30 · p. 1
Magnetic Metal Complexes 2024-12-16 · p. 1
C-H Bond Activation Reaction 2025-06-20 · p. 8
Transition Metal Catalysts 2026-04-10 · p. 8

Related TCI products

C-H Activation Studies: This compound is ideal for C-H activation due to its ability to facilitate the breaking and forming of carbon-hydrogen bonds, making it essential for exploring new catalytic mechanisms.
Organic Synthesis Reactions: Its reactivity and stability make it a valuable catalyst in organic synthesis, particularly in substitution and oxidation reactions where precise control is required.
Inorganic Chemistry Research: The compound’s unique electronic properties enable it to participate in various inorganic reactions, supporting studies in coordination chemistry and metal-based catalysis.
Catalytic Oxidation Processes: Its ability to act as an efficient catalyst in oxidation reactions makes it suitable for applications in environmental and industrial chemistry.
Reductive Reaction Systems: The compound’s versatility allows it to be used in reductive processes, where it can facilitate the reduction of various organic and inorganic compounds.

Brand	TCI
CAS number	16456-81-8
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis]
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

Iron(III) Tetraphenylporphyrin Chloride should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is best stored in a well-ventilated area to minimize any potential risks associated with its use. Proper storage conditions help ensure the compound remains effective for use in laboratory experiments. Always follow standard laboratory safety protocols when handling this material.

References cited in the TCI brochure

Xu-cheng Gan. Iron-Catalyzed Hydrobenzylation: Stereoselective Synthesis of (−)-Eugenial C Journal of the American Chemical Society, 2023. doi:10.1021/jacs.3c05428
Nathan Dao. Metal-Hydride C–C Cross-Coupling of Alkenes Through a Double Outer-Sphere Mechanism The Journal of Organic Chemistry, 2024. doi:10.1021/acs.joc.4c00260
Xu-cheng Gan. Carbon quaternization of redox active esters and olefins by decarboxylative coupling Science, 2024. doi:10.1126/science.adn5619