Skip to Content
Merck
CN

121908

Neocuproine hydrate

99%

Synonym(s):

2,9-Dimethyl-1,10-phenanthroline hydrate

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C14H12N2 · xH2O
CAS Number:
Molecular Weight:
208.26 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-601-9
MDL number:
Assay:
99%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

MFZBSWSCIWCRKS-UHFFFAOYSA-N

InChI

1S/C14H12N2.H2O/c1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9;/h3-8H,1-2H3;1H2

SMILES string

[H]O[H].Cc1ccc2ccc3ccc(C)nc3c2n1

assay

99%

solubility

methanol: soluble 50 mg/mL, clear, colorless to dark yellow

Quality Level

General description

Neocuproine hydrate is chelating agent and forms complex with Cu+ formed by reduction of Cu+2 by hydroxylamine hydrochloride and produces electrochemiluminescence. It is an efficient ligand for alcohol oxidation with palladium in 1:1 water/DMSO mixtures.

Application

Neocuproine hydrate was used in determination of copper ions in aqueous solution using electrochemiluminescence.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Determining copper ions in water using electrochemiluminescence.
High B, et al.
Analytica Chimica Acta, 449(1), 17-22 (2001)
Catalytic Conversions in Water. Part 23: Steric Effects and Increased Substrate Scope in the Palladium-Neocuproine Catalyzed Aerobic Oxidation of Alcohols in Aqueous Solvents#.
Brink GJ, et al.
Advanced Synthesis & Catalysis, 345(12), 1341-1352 (2003)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service