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Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate

  • CAS No. 1257642-74-2

  • Cat. No. CS-0540031
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate|CS-0540031

Structure of 1257642-74-2

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General Information

  • CAS No. 1257642-74-2
  • Cat. No. CS-0540031
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature, keep dry and cool
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₆H₂₀N₂Na₂O₇S₂
  • Molecular Weight 582.56
  • Synonym(s) Bathocuproinedisulfonic acid disodium salt hydrate
  • SMILES CC1=C(C(=C2C=CC3=C(C(=C(N=C3C2=N1)C)S(=O)(=O)[O-])C4=CC=CC=C4)C5=CC=CC=C5)S(=O)(=O)[O-].O.[Na+].[Na+]

Description

Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate delivers a highly water-soluble chelating ligand featuring two sulfonate groups and sterically shielded phenanthroline core. This robust complexing agent enables efficient metal coordination under physiological conditions, offering enhanced stability and solubility for biochemical applications.

Application

Sodium 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate hydrate functions as a water-soluble chelating ligand, enabling efficient coordination to transition metals in catalytic systems. Its sulfonate groups enhance solubility and stability in aqueous media, while the rigid phenanthroline core provides strong metal binding affinity. This compound serves as a versatile building block in homogeneous catalysis and metal complex synthesis, particularly for applications requiring hydrophilic character and robust ligand performance under physiological or aqueous conditions.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H413
Precautionary Statements : P264-P270-P273-P330-P501

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Computational Chemistry Data

  • TPSA   171.68
  • LogP   -2.27466
  • H_Acceptors   8
  • H_Donors   0
  • Rotatable_Bonds   4

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