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Neocuproine

Neocuproine Structure
CAS No.
484-11-7
Chemical Name:
Neocuproine
Synonyms
2,9-DIMETHYL-1,10-PHENANTHROLINE;DMPHEN;Mephen;2,9-Dimethylphenanthroline;2,9-Dimethyl-o-phenanthroline;VUF 7738;NEOCUPROINE;Cuproin,neo;Neo-Cuproin;2,9-DimethyL
CBNumber:
CB0429520
Molecular Formula:
C14H12N2
Molecular Weight:
208.26
MOL File:
484-11-7.mol
MSDS File:
SDS
Modify Date:
2024/6/3 14:46:32

Neocuproine Properties

Melting point 159-164 °C
Boiling point 337.46°C (rough estimate)
Density 1.1345 (rough estimate)
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
InChIKey IYRGXJIJGHOCFS-UHFFFAOYSA-N
CAS DataBase Reference 484-11-7(CAS DataBase Reference)
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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
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  Yes
HS Code  29339990
NFPA 704
0
2 0

Neocuproine price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) N1501 Neocuproine ≥98% 484-11-7 1G ₹4286.7 2022-06-14 Buy
Sigma-Aldrich(India) N1501 Neocuproine ≥98% 484-11-7 5G ₹13076.6 2022-06-14 Buy
Sigma-Aldrich(India) N1501 Neocuproine ≥98% 484-11-7 25G ₹26337.23 2022-06-14 Buy
Sigma-Aldrich(India) 1.02968 Neocuproine GR for analysis 484-11-7 5G ₹22250 2022-06-14 Buy
ottokemi N 1377 Neocuproine , GR 99%+ 484-11-7 1gm ₹1341 2022-05-26 Buy
Product number Packaging Price Buy
N1501 1G ₹4286.7 Buy
N1501 5G ₹13076.6 Buy
N1501 25G ₹26337.23 Buy
1.02968 5G ₹22250 Buy
N 1377 1gm ₹1341 Buy

Neocuproine Chemical Properties,Uses,Production

Chemical Properties

OFF-WHITE TO VERY PALE YELLOW CRYSTALLINE POWDER

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.

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.]

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TIMTEC-BB SBB008718 NEOCUPROINE REAG NEOCUPROINE 10-Phenanthroline,2,9-dimethyl-1 2,9-dimethyl-10-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 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- Neocuproine, 98.5% 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 2,9-Dimethyl-o-phenanthroline 2,9-Dimethylphenanthroline Mephen DMPHEN 2,9-DIMETHYL-1,10-PHENANTHROLINE Neocuproine、2,9-Dimethyl-1,10-phenanthroline hemihydrate 484-11-7 C14H12N212H2O CH32C12H6N2 C14H12N205H2O Chelating Reagents Phenanthrolines Analytical Reagents Analytical Chromatography Product Catalog General Use Puriss p.a. Analytical Chemistry Chelating Reagents