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2,9-Dimethyl-1,10-phenanthrolin

2,9-Dimethyl-1,10-phenanthroline

HCID 65237
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Grundinformationen

CAS
484-11-7
Standard-SMILES
Cc1ccc2ccc3ccc(C)nc3c2n1
InChIKey
IYRGXJIJGHOCFS-UHFFFAOYSA-N
Summenformel
C14H12N2
Durchschnittliche Molmasse
208,26 g/mol
Monoisotopische Masse
208,10004839

Überblick

Neocuproine is a member of the class of phenanthrolines that is 1,10-phenanthroline bearing two methyl substituents at positions 2 and 9. It has a role as a copper chelator and a chelator.

Namen und Bezeichner

Bevorzugter Name
2,9-Dimethyl-1,10-phenanthroline
IUPAC
2,9-dimethyl-1,10-phenanthroline
Lokaler Name
2,9-Dimethyl-1,10-phenanthrolin
Englischer Name
Neocuproine
Summenformel
C14H12N2
Molmasse
208.26

Namen und Synonyme

Neocuproine2,9-Dimethyl-1,10-phenanthroline484-11-7Neocuproin1,10-Phenanthroline, 2,9-dimethyl-2,9-DimethylphenanthrolineDMPHEN2,9-Dimethyl-o-phenanthroline8E7D2SH3BVDTXSID5060065NSC-4280VUF-7738
Weitere Namen anzeigen
Mephen2,9-dimethyl-10-phenanthrolineVUF 7738Cuproin,neo
CHEBI:912223,6-dimethyl-4,5-phenanthrolineRefChem:165152DTXCID1040619207-601-9neo-CuproinNSC4280MFCD00004973

Datenbank-Bezeichner

CAS
484-11-7、7296-20-0
PubChem CID
65237
DTXSID
DTXSID5060065
ChEMBL
CHEMBL375781
ChEBI
CHEBI:91222
UNII
8E7D2SH3BV
EC Number
207-601-9、230-732-8
Nikkaji

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3,3
Polarare Oberfläche (TPSA)
25,8 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
2
Frei drehbare Bindungen
0
Schwere Atome
16
Formalladung
0
Komplexität
227

Experimentelle und physikochemische Eigenschaften

PolymersOther Classes -> Polycyclic Aromatic Hydrocarbons
SpringerMaterials PropertiesCrystal structure
LogP2.46
Physical DescriptionBeige crystalline solid; [Sigma-Aldrich MSDS]

Physikochemische Eigenschaften

Schmelzpunkt
159 · 159-164 °C
Siedepunkt
337.46 °C · 337.46°C (rough estimate)
Dichte
1.1345 · 1.1345 (rough estimate)
Brechungsindex
1.6152 · 1.6152 (estimate)
storage temp.
Keep in dark place,Sealed in dry,Room Temperature
Löslichkeit
0.1 g/mL, · methanol: 0.1 g/mL, clear
Aggregatzustand
crystalline
pka
6.01 · 6.01±0.30(Predicted)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

This chemical does not meet GHS hazard criteria for 2.1% (1 of 47) of reports.

Warning

H315 (97.9%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 47 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Warning

Gefahrenhinweise

Regulatory Information · 2 Einträge

Chemical: 1,10-Phenanthroline, 2,9-dimethyl-

1,10-Phenanthroline, 2,9-dimethyl-: Does not have an individual approval but may be used under an appropriate group standard

Hazards SummaryA skin and strong eye irritant; [Sigma-Aldrich MSDS] See POLYCYCLIC AROMATIC HYDROCARBONS.
Hazard Classes and Categories · 2 Einträge

Skin Irrit. 2 (100%)

Skin Irrit. 2 (97.9%)

Sicherheitsdaten

wgk
3
tsca
TSCA listed
hs_code
2933990099
risk_code
36/37/38-20/21/22-22
hazard_code
Xi,Xn
safety_code
26-36/37/39-36-24/25
Speicherklasse
11 - Combustible Solids

Chemie und Industrie

Pharmakologische Informationen

MeSH Pharmacological Classification · 2 Einträge

Substances that inhibit or prevent the proliferation of NEOPLASMS.

Chemicals that bind to and remove ions from solutions. Many chelating agents function through the formation of COORDINATION COMPLEXES with METALS.

Verwendung und Herstellung

UsesUsed as a reagent in assays (blood glucose and spectrophotometric determination of copper); [Merck Index]
General Manufacturing Information1,10-Phenanthroline, 2,9-dimethyl-: ACTIVE
Anwendungen · 1 Eintrag

VerwendenDue 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.

Zugehörige Reaktionen

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Reaktionsgleichung von HRID 202172
HRID 202172als EduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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Reaktionsgleichung von HRID 257614
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Reaktionsgleichung von HRID 516426
HRID 516426als Eduktuspto-grants-2015_08
Reaktionsgleichung von HRID 516427
HRID 516427als Eduktuspto-grants-2015_08
Reaktionsgleichung von HRID 622653
HRID 622653als Eduktuspto-grants-1988_09
Reaktionsgleichung von HRID 666378
HRID 666378als EduktTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaktionsgleichung von HRID 1308832
HRID 1308832als KatalysatorHigh-throughput exploration of 50,688 Pd-, Ni- and Cu-catalysed C–N coupling reactions
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J5.993E
Farbe
white to beige
Wasserlöslichkeit
slightly soluble
Merck
6449 · 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 · 484-11-7(CAS DataBase Reference)
NIST chemische Informationen
1 · 1,10-Phenanthroline, 2,9-dimethyl-(484-11-7)
EPA chemische Informationen
1 · 1,10-Phenanthroline, 2,9-dimethyl- (484-11-7)

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

Copper(1+)bis(2,9-diMethyl- 1,10-phenanthrolineEthenamine, 2,2'-(2,3-dinitro-1,4-phenylene)bis[N,N-dimethyl-, (E,E)- (9CI)1,4-dimethyl-2,3-dinitrobenzene8-AminoquinaldineEthylvinylether

Nachgelagerte Produkte

2,2'-Bipyridil1,10-Phenanthroline-2,9-dicarboxylic acid1,10-Phenanthroline, 2,9-bis(bromomethyl)-

Ergänzende Hinweise

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