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    Neocuproine hemihydrate

    Available from stock

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      Neocuproine hemihydrate

      SKU
      N0115

      Category: Fluorescent Detection

      Synonyms
      2,9-Dimethyl-1,10-phenanthroline, DMPHEN, NSC 4280, VUF 7738
      484-11-7
      CAS-Number
      C14H12N2 · 0.5H2O
      Molecular Formula
      217.27
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥99% (Assay)
      Appearance
      White to light yellow powder
      Identity
      1H-NMR
      Water content (K.F.)
      ≤5%

      Properties

      Solvents
      Soluble in methanol (50 mg/ml), ethanol (10 mg/ml) or DMSO (25 mg/ml).
      Melting Point
      159 - 164 °C

      Documentation

      Safety Data Sheet (SDS)
      CDX N0115 SDS.pdf
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Hazard statements
      H302 - H315 - H318 - H335
      Precautionary statements
      P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310
      GHS Symbol
      GHS05+GHS07
      Signal word
      Danger
      Transportation
      Not dangerous goods
      Description
      Neocuproine is a complexing reagents, known for its ability to form stable complexes with metal ions, particularly CU2+ ions. This property makes it valuable in various analytical and research applications, including spectrophotometry and electrochemistry. In the presence of CU2+ ions, neocuproine forms a brightly colored complex that can be used for the quantitative determination of copper in solution. The Neocuproine-CU2+ complex exists in a 2:1 ratio with a maximum absorption at 454 nm. Neocuproine is used in complex with Cu2+ as chromogenic oxidant in the total antioxidant capacity assay (CUPRAC method). In addition to its analytical uses, neocuproine and its derivatives have been employed in the field of coordination chemistry to study and synthesize metal complexes. These complexes often have unique properties and are of interest for their potential applications in catalysis, material science, and other areas of chemical research. This compound is also widely used in some biomedical fields, such as in the study of copper metabolism disorders and neurodegenerative diseases and neocuproine-CU2+ complexes have shown biological properties, such as antitumor activity.
      Smiles
      Cc1ccc2ccc3ccc(C)nc3c2n1
      References
      (1) A. Mohindru, et al., Biochem. Pharmacol. 32, 3627 (1983) , (2) H.H. Al-Sa′doni, et al., Br. J. Pharmacol. 121, 1047 (1997) , (3) J.G. De Man, et al., Eur. J. Pharmacol. 381, 151 (1999) , (4) R. Apak, et al., Free Radic. Res. 39, 949 (2005) , (5) A.A. Gouda & A.S. Amin, Arabian J. Chem. 3, 159 (2010) , (6) O.V. Patel, et al., Biometals 26, 415 (2013) , (7) K.A. Jesse, et al., Inorg. Chem. 58, 9057 (2019)

      Neocuproine is a complexing reagents, known for its ability to form stable complexes with metal ions, particularly CU2+ ions. This property makes it valuable in various analytical and research applications, including spectrophotometry and electrochemistry. In the presence of CU2+ ions, neocuproine forms a brightly colored complex that can be used for the quantitative determination of copper in solution. The Neocuproine-CU2+ complex exists in a 2:1 ratio with a maximum absorption at 454 nm. Neocuproine is used in complex with Cu2+ as chromogenic oxidant in the total antioxidant capacity assay (CUPRAC method). In addition to its analytical uses, neocuproine and its derivatives have been employed in the field of coordination chemistry to study and synthesize metal complexes. These complexes often have unique properties and are of interest for their potential applications in catalysis, material science, and other areas of chemical research. This compound is also widely used in some biomedical fields, such as in the study of copper metabolism disorders and neurodegenerative diseases and neocuproine-CU2+ complexes have shown biological properties, such as antitumor activity.

      SKU: N0115 Category: Fluorescent Detection
      • Additional information

      Additional information

      Synonyms

      2,9-Dimethyl-1,10-phenanthroline, DMPHEN, NSC 4280, VUF 7738

      Purity

      ≥99% (Assay)

      Appearance

      White to light yellow powder

      CAS-Number

      484-11-7

      Molecular Formula

      C14H12N2 · 0.5H2O

      Molecular Weight

      217.27

      Identity

      1H-NMR

      Solvents

      Soluble in methanol (50 mg/ml), ethanol (10 mg/ml) or DMSO (25 mg/ml).

      Melting Point

      159 – 164 °C

      Smiles

      Cc1ccc2ccc3ccc(C)nc3c2n1

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Hazard statements

      H302 – H315 – H318 – H335

      Precautionary statements

      P280 – P301 + P312 + P330 – P302 + P352 – P305 + P351 + P338 + P310

      GHS Symbol

      GHS05+GHS07

      Signal word

      Danger

      Transportation

      Not dangerous goods

      References

      (1) A. Mohindru, et al., Biochem. Pharmacol. 32, 3627 (1983), (2) H.H. Al-Sa′doni, et al., Br. J. Pharmacol. 121, 1047 (1997), (3) J.G. De Man, et al., Eur. J. Pharmacol. 381, 151 (1999), (4) R. Apak, et al., Free Radic. Res. 39, 949 (2005), (5) A.A. Gouda & A.S. Amin, Arabian J. Chem. 3, 159 (2010), (6) O.V. Patel, et al., Biometals 26, 415 (2013), (7) K.A. Jesse, et al., Inorg. Chem. 58, 9057 (2019)

      Quantity

      25 g, 100 g, Bulk

      cdx-Water content (K.F.)

      ≤5%

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