Bathocuproine (purified by sublimation) TCI B2694

Chemical Identity

CAS No.: 4733-39-5
PubChem: CID 65149·SID 87558362
Formula: C26H20N2
Molecular weight: 360.4 g/mol
Purity: >99.0%(HPLC)(T)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline
SMILES: CC1=CC(=C2C=CC3=C(C=C(N=C3C2=N1)C)C4=CC=CC=C4)C5=CC=CC=C5
InChIKey: STTGYIUESPWXOW-UHFFFAOYSA-N

Rp 5.830.650,00

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Bathocuproine is a chemical compound widely used as a nitrogen-donor ligand in catalytic reactions and organic synthesis. It plays a crucial role in laboratory settings by facilitating the formation of stable metal-ligand complexes, which are essential in various chemical processes. This compound is particularly valuable in catalysis due to its ability to interact with transition metal ions, making it a key component in the development of efficient catalytic systems. Its versatility allows it to be applied across multiple fields of chemistry, including inorganic and coordination chemistry.

One of the main reasons Bathocuproine is preferred is its structural complexity and its capacity to bind with a variety of metal ions such as copper, silver, and tin. These properties enable it to modify catalytic activity and enhance the specificity of chemical reactions. Additionally, its stability under certain conditions makes it a reliable choice for researchers aiming to achieve consistent results in their experiments. The compound's ability to act as a ligand in diverse chemical environments further contributes to its popularity in both academic and industrial research.

In Indonesian laboratories, Bathocuproine is commonly used by chemists and material scientists to expand their understanding of catalytic reactions and complex synthesis. Its presence in research settings supports the development of new chemical methodologies and contributes to advancements in both theoretical and applied chemistry. As a result, it remains a fundamental tool for those working in the field of catalysis and inorganic chemistry.

TCI brochures (PDF)

Electron Transport Material for OLED NBPhen 2025-02-27 · p. 1
Chemical Compounds Purified by Sublimation 2025-05-07 · p. 4
Organic Light-Emitting Diode (OLED) Materials 2026-08-18 · p. 6
Solar Cell Materials 2026-04-21 · p. 9
Ligands 2025-12-01 · p. 15

Related TCI products

Catalytic Reaction Development: Bathocuproine is ideal for designing new catalytic systems due to its ability to form stable metal-ligand complexes, enhancing reaction efficiency and selectivity.
Organic Synthesis Research: Its role as a nitrogen-donor ligand makes it suitable for organic synthesis, where it helps in the formation of complex molecular structures with high precision.
Inorganic Chemistry Studies: The compound is frequently used in inorganic chemistry to investigate metal-ligand interactions and their impact on reaction mechanisms.
Coordination Chemistry Experiments: Its capacity to bind with various metal ions makes it a valuable tool for studying coordination compounds and their properties.
Material Science Investigations: Researchers use Bathocuproine to explore its potential in creating new materials with unique catalytic properties and structural characteristics.

Brand	TCI
CAS number	4733-39-5
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > Nitrogen-Donor Ligands [Catalysis]
Pack sizes	As listed on product page
Physical form	Solid
Storage	Store in a cool, dry place away from light

Bathocuproine should be stored in a cool, dry environment, away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to incompatible substances, and ensure proper ventilation when working with the compound. Storage conditions should be consistent to preserve its stability and effectiveness in laboratory applications. Always follow standard safety protocols to minimize risks during handling and experimentation.

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