Chemodex

Neocuproine hydrochloride monohydrate

CHF 122.00
In stock
CDX-N0114-G0055 gCHF 122.00
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Product Details
Synonyms 2,9-Dimethyl-1,10-phenanthroline hydrochloride; DMPHEN; NSC 4280; VUF 7738
Product Type Chemical
Properties
Formula C14H12N2 . HCl . H2O
MW 262.73
CAS 303136-82-5
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (NMR)
Appearance White to off-white powder.
Solubility Soluble in water (25mg/ml) or DMSO.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key APDYLFLZNGECIM-UHFFFAOYSA-N
Smiles CC1=NC2=C(C=C1)C=CC3=CC=C(C)N=C23.Cl.O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
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Product Specification Sheet
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Description

Neocuproine is a complexing reagent, 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.

Product 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)

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