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Neocuproine

CAS No.
484-11-7
Chemical Name:
Neocuproine
Synonyms
2,9-DIMETHYL-1,10-PHENANTHROLINE;DMPHEN;Mephen;2,9-Dimethylphenanthroline;2,9-dimethyl-10-phenanthroline;2,9-Dimethyl-o-phenanthroline;VUF 7738;NEOCUPROINE;Cuproin,neo;Neo-Cuproin
CBNumber:
CB0429520
Molecular Formula:
C14H12N2
Molecular Weight:
208.26
MDL Number:
MFCD00004973
MOL File:
484-11-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-10-21 17:18:09

Neocuproine Properties

Melting point 159-164 °C
Boiling point 337.46°C (rough estimate)
Density 1.1345 (rough estimate)
bulk density 280kg/m3
refractive index 1.6152 (estimate)
RTECS SF8380000
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility methanol: 0.1 g/mL, clear
form crystalline
pka 6.01±0.30(Predicted)
color white to beige
Water Solubility slightly soluble
Sensitive Light Sensitive
Merck 6449
InChI 1S/C14H12N2/c1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9/h3-8H,1-2H3
InChIKey IYRGXJIJGHOCFS-UHFFFAOYSA-N
SMILES Cc1ccc2ccc3ccc(C)nc3c2n1
CAS DataBase Reference 484-11-7(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 8E7D2SH3BV
NIST Chemistry Reference 1,10-Phenanthroline, 2,9-dimethyl-(484-11-7)
EPA Substance Registry System 1,10-Phenanthroline, 2,9-dimethyl- (484-11-7)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi,Xn
Risk Statements  36/37/38-20/21/22-22
Safety Statements  26-36/37/39-36-24/25
WGK Germany  3
TSCA  TSCA listed
HS Code  29339990
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

Neocuproine price More Price(69)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich N1501 Neocuproine ≥98% 484-11-7 1g $39.7 2026-04-30 Buy
Sigma-Aldrich N1501 Neocuproine ≥98% 484-11-7 5g $119 2026-04-30 Buy
Sigma-Aldrich 1.02968 Neocuproine GR for analysis 484-11-7 5G $260 2026-04-30 Buy
Cayman Chemical 20874 Neocuproine ≥98% 484-11-7 5g $60 2026-04-30 Buy
Cayman Chemical 20874 Neocuproine ≥98% 484-11-7 10g $104 2026-04-30 Buy
Product number Packaging Price Buy
N1501 1g $39.7 Buy
N1501 5g $119 Buy
1.02968 5G $260 Buy
20874 5g $60 Buy
20874 10g $104 Buy

Neocuproine Chemical Properties, Uses, Production

Chemical Properties

Neocuproine is a off-white to very pale yellow crystalline powder, in the presence of reducing agents it reacts with copper to give a copper(I) complex of composition MA2 and of tetrahedral symmetry.

Uses

Due to the steric hindrance of the methyl groups attached to the carbon atoms adjacent to the nitrogen donor atoms of phenanthroline, the reagent does not give the low spin vivid red complex characteristic of phenanthroline derivatives with iron(II). However, in the presence of reducing agents it reacts with copper to give a copper(I) complex of composition MA2 and of tetrahedral symmetry. This chelate is insoluble in water and can be extracted by chloroform in which the absorption maximum of the complex appears at 457 nm. In this way the concentration of the complex can be measured. The method is suitable for the determination of copper in iron, manganese and vanadium ores even in the presence of aluminium, germanium, titanium and silicon.
Neocuproine is today considered one of the most selective reagents. Unfortunately, it is rather expensive. 2,3-bis-(2-pyridyl)quinoxaline, prepared by Belcher et al. by condensation of o-diketone, 2,2'-dipyridyl and 0-phenylenediamine(44) contains the functional grouping characteristic of cuproine; it is quite suitable for the determination of copper and it is cheap. Starting with various substituted o-phenylene-diamines Belcher synthesized 25 different quinoxaline derivatives, of which 2,3-bis-[2-(-methyl)-pyridyl)]quinoxaline proved to be identical with neocuproine as regards analytical selectivity. Besides copper, titanium(III) is the only metal ion which gives a colour reaction with the reagent. However, the coloured titanium(III) complex is formed only at lower pH and hence it does not interfere with the determination of copper. The copper complex of the reagent can be extracted quantitatively with isopentyl alcohol usually as a perchlorate ion pair.

Uses

Neocuproine is a phenanthroline based metal ion chelating agent.

Definition

ChEBI: A member of the class of phenanthrolines that is 1,10-phenanthroline bearing two methyl substituents at positions 2 and 9.

Purification Methods

Purifiy it as the hemihydrate by crystallisation from water and as the anhydrous base from *benzene. [Beilstein 23/8 V 527.]

113397-69-6
484-11-7
Synthesis of Neocuproine from Ethenamine, 2,2'-(2,3-dinitro-1,4-phenylene)bis[N,N-dimethyl-, (E,E)- (9CI)
Global Suppliers ( 349)
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Nantong puyue biomedical Co., Ltd 0513-0513-0513-89158300 18014392889 sales@puyerbiopharma.com China 4956 58
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INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66
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TAIYUAN RHF CO.,LTD. +86 351 7031519 sales@RHFChem.com China 2334 56

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View Latest Price from Neocuproine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,9-Dimethyl-1,10-phenanthroline pictures 2026-10-21 2,9-Dimethyl-1,10-phenanthroline
484-11-7
$12.00-104.00 1g 0.98 10kg Shanghai UCHEM Inc.
Neocuproine pictures 2026-10-21 Neocuproine
484-11-7
10g 99% 1 KG Shanghai Massive Chemical Technology Co., Ltd
Neocuproine pictures 2026-07-22 Neocuproine
484-11-7
1kg 99% 20MT Watson Biotechnology Co.,Ltd
  • Neocuproine pictures
  • Neocuproine
    484-11-7
  • 99%
  • Shanghai Massive Chemical Technology Co., Ltd
  • Neocuproine pictures
  • Neocuproine
    484-11-7
  • $0.00
  • 99%
  • Watson Biotechnology Co.,Ltd
TIMTEC-BB SBB008718 NEOCUPROINE REAG NEOCUPROINE 10-Phenanthroline,2,9-dimethyl-1 2,9-Dimethyl-o-phenanthroline 2,9 DiMethy 1,10-phenanthrofine Neocuproine, 99+% 5GR NEOCUPROINE GR FOR ANALYSIS 5 G 2,9- twoMethyl -1,10-phen 2,9-Neocuproine VUF 7738 Cuproin,neo 2,9-dimethyl-1,10-phenanthroline,98% Neocuproine hemihydrate,2,9-Dimethyl-1,10-phenanthroline Neocuproine,2,9-Dimethyl-1,10-phenanthroline Neocuproine Hemihydr Neocuproine, 98.5% Neocuproine Vetec(TM) reagent grade, 98% 2,10-diMethyl-1,9-phenanthroline Neocuproine HeMihydrat Neo-Cuproin Neocuproin,hemihydrate neocuproine free base Neocuproine,98% NEOCUPROIN HEMIHYDRATE R. G. NeocuproineGr Neocuproine, 99+% NEOCUPROINE,REAGENT 2,9-DIMETHYL-1,10-PHENANTHROLINE REAGENT (ACS) 1,10-Phenanthroline, 2,9-dimethyl- 2,9-DIMETHYL-1,10-PHENANTHROLINE, REAGENT (ACS)2,9-DIMETHYL-1,10-PHENANTHROLINE, REAGENT (ACS)2,9-DIMETHYL-1,10-PHENANTHROLINE, REAGENT (ACS)2,9-DIMETHYL-1,10-PHENANTHROLINE, REAGENT (ACS) Neocuproine, 98.5%, reagent grade 2,9-DimethyL ine hemihydrate -1,10-phenanthroL Neocuproin hemihydrate, Reag. Neocuproine, 95%+ Neocuproine, GR 99%+ Neocuproine (2,9-Dimethyl-1,10-phenanthroline) extrapure, 99% 3-Dihydroflavone Neocuproine、2,9-Dimethyl-1,10-phenanthroline hemihydrate Neocuproine 99% AR 2,9-Dimethylphenanthroline 2,9-dimethyl-10-phenanthroline 2,9-DIMETHYL-1,10-PHENANTHROLINE DMPHEN Mephen 484-11-7 C14H12N212H2O CH32C12H6N2 C14H12N205H2O Chelating Reagents Phenanthrolines Analytical Reagents Analytical Chromatography Product Catalog General Use Puriss p.a. Analytical Chemistry