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CAS 4733-39-5

Bathocuproine TCI D0711

Bathocuproine TCI D0711

Chemical Identity

Other names
2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline
CAS No.
4733-39-5
Formula
C26H20N2
Molecular weight
360.46 g/mol
Purity
>95.0%(T)(HPLC)
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
MDL
MDL00004972
PubChem
CID 65149
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Bathocuproine is a chemical compound widely used in various chemical reactions, particularly in the fields of catalysis and inorganic chemistry. It serves as a key ligand in the synthesis of metal complexes, especially those involving transition metals like copper. In the laboratory, it functions as a versatile reagent that supports the creation of stable and specific reaction environments. Its role is critical in facilitating the coordination of metal ions, which is essential for many synthetic processes.

The compound is valued for its stable molecular structure and its ability to donate electrons, making it an effective nitrogen-donor ligand. These properties allow it to interact efficiently with transition metals, enhancing the reactivity and selectivity of chemical reactions. Its consistent chemical behavior also makes it a reliable choice for research involving metal reactivity and reaction mechanisms.

In Indonesian laboratories, Bathocuproine is commonly used in scientific research, particularly in chemistry and catalysis. It is frequently found in university laboratories and research institutions focused on the synthesis of chemical compounds and the study of metal interactions. Its reliability and effectiveness have made it a preferred material for various experimental setups.

  • Metal Complex Synthesis: Bathocuproine is ideal for synthesizing metal complexes due to its ability to coordinate with transition metals like copper, enhancing the stability and reactivity of the resulting compounds.
  • Catalytic Reactions: It is widely used in catalytic processes where stable and specific reaction environments are required, supporting the formation of desired products with high efficiency.
  • Reaction Environment Stabilization: Its molecular stability allows it to maintain consistent reaction conditions, which is crucial for reproducible and reliable experimental results.
  • Metal Reactivity Studies: The compound's consistent chemical behavior makes it suitable for investigating the reactivity of metals and the mechanisms of chemical reactions.
  • Ligand-Based Research: It is a preferred ligand in nitrogen-donor studies, supporting the development of new synthetic methods and the understanding of coordination chemistry.

Brand TCI
CAS number 4733-39-5
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Nitrogen-Donor Ligands [Catalysis]
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

Bathocuproine should be stored in a cool, dry place, away from light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which could degrade its chemical properties. In laboratory settings, it should be handled with care to avoid direct contact with skin and eyes, although it is generally considered safe under normal conditions. It is important to ensure that the storage area is well-ventilated to prevent the accumulation of any potentially harmful vapors. Proper labeling of containers is also essential to ensure safe handling and prevent accidental misuse.

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