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CAS 1662-01-7

Bathophenanthroline (purified by sublimation) TCI B2695

Bathophenanthroline (purified by sublimation) TCI B2695

Chemical Identity

CAS No.
1662-01-7
PubChem
CID 72812·SID 87558363
Formula
C24H16N2
Molecular weight
332.4 g/mol
Purity
>99.0%(HPLC)(T)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4,7-diphenyl-1,10-phenanthroline
SMILES
C1=CC=C(C=C1)C2=C3C=CC4=C(C=CN=C4C3=NC=C2)C5=CC=CC=C5
InChIKey
DHDHJYNTEFLIHY-UHFFFAOYSA-N
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Bathophenanthroline (purified by sublimation), with the CAS number 1662-01-7, is a nitrogen-donor ligand widely used in chemical reactions and laboratory analysis. It is a key component in the field of inorganic chemistry and catalysis, where it plays a crucial role in the synthesis of metal complexes and catalytic processes. Its unique molecular structure, consisting of three aromatic rings and four amino groups, allows it to act as a versatile ligand in various chemical environments. This compound is particularly valued for its stability and reactivity, making it a reliable choice for researchers working in both academic and industrial settings.

The chemical properties of Bathophenanthroline make it a preferred choice in laboratory settings. It exhibits high reactivity and the ability to form stable metal complexes, which is essential for analytical and synthetic applications. Its capacity to bind with specific metals also enhances its utility in quantitative analysis. These characteristics ensure that it remains a valuable tool in the study of inorganic chemistry and catalytic reactions, supporting accurate and reproducible results in laboratory experiments.

In Indonesian laboratories, Bathophenanthroline is commonly used in scientific research, especially in the fields of inorganic chemistry and catalysis. It is frequently found in university laboratories and research institutions due to its wide range of applications and reliability. Its presence in these settings highlights its importance in advancing chemical research and analytical techniques within the Indonesian scientific community.

  • Metal complex synthesis: Bathophenanthroline is ideal for forming stable metal complexes, making it essential in coordination chemistry studies.
  • Catalytic reactions: Its reactivity and ligand properties make it suitable for catalytic processes in organic and inorganic chemistry.
  • Quantitative analysis: The compound's ability to bind with specific metals aids in accurate and precise analytical techniques.
  • Inorganic chemistry research: It supports the study of metal-ligand interactions and structural analysis in anorganic compounds.
  • Laboratory teaching: Its stability and reactivity make it a valuable tool for demonstrating chemical reactions and ligand behavior in educational settings.

Brand TCI
CAS number 1662-01-7
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Nitrogen-Donor Ligands [Catalysis]
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light and moisture

Bathophenanthroline should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which can affect its stability. As a nitrogen-donor ligand, it is generally non-toxic but should be handled with care in laboratory settings to avoid direct contact. Proper ventilation is advised when working with the compound to ensure a safe environment. Laboratory personnel should follow standard safety protocols when handling and storing this material to minimize any potential risks.

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