2,9-Dimethyl-1,10-phenanthrolin

Neocuproine Struktur
484-11-7
CAS-Nr.
484-11-7
Bezeichnung:
2,9-Dimethyl-1,10-phenanthrolin
Englisch Name:
Neocuproine
Synonyma:
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
Summenformel:
C14H12N2
Molgewicht:
208.26
MOL-Datei:
484-11-7.mol

2,9-Dimethyl-1,10-phenanthrolin Eigenschaften

Schmelzpunkt:
159-164 °C
Siedepunkt:
337.46°C (rough estimate)
Dichte
1.1345 (rough estimate)
chüttdichte
280kg/m3
Brechungsindex
1.6152 (estimate)
RTECS-Nr.
SF8380000
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Löslichkeit
methanol: 0.1 g/mL, clear
Aggregatzustand
crystalline
pka
6.01±0.30(Predicted)
Farbe
white to beige
Wasserlöslichkeit
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 Datenbank
484-11-7(CAS DataBase Reference)
NIST chemische Informationen
1,10-Phenanthroline, 2,9-dimethyl-(484-11-7)
EPA chemische Informationen
1,10-Phenanthroline, 2,9-dimethyl- (484-11-7)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi,Xn
R-Sätze: 36/37/38-20/21/22-22
S-Sätze: 26-36/37/39-36-24/25
WGK Germany  3
TSCA  TSCA listed
HS Code  29339990
Speicherklasse 11 - Combustible Solids
Bildanzeige (GHS) Exclamation Mark (GHS07)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung
Sicherheit
P261 Einatmen von Staub vermeiden.
P304+P340 BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P405 Unter Verschluss aufbewahren.

2,9-Dimethyl-1,10-phenanthrolin Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R20/21/22:Gesundheitsschädlich beim Einatmen,Verschlucken und Berührung mit der Haut.
R22:Gesundheitsschädlich beim Verschlucken.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

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.

Verwenden

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.

läuterung methode

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

2,9-Dimethyl-1,10-phenanthrolin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


2,9-Dimethyl-1,10-phenanthrolin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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484-11-7(2,9-Dimethyl-1,10-phenanthrolin)Verwandte Suche:


  • 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
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