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35020

Supelco

2,2′-Biquinoline

for spectrophotometric det. of Cu, ≥99.0%

Sinónimos:

2,2′-Diquinolyl, Cuproin

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About This Item

Fórmula empírica (notación de Hill):
C18H12N2
Número de CAS:
119-91-5
Peso molecular:
256.30
Beilstein/REAXYS Number:
187259
EC Number:
204-357-5
MDL number:
MFCD00006740
UNSPSC Code:
41116105
PubChem Substance ID:
329755111
NACRES:
NA.21

Quality Level

100

assay

≥99.0% (NT)
≥99.0%

quality

for spectrophotometric det. of Cu

technique(s)

UV/Vis spectroscopy: suitable

ign. residue

≤0.05%

mp

192-195 °C (lit.)
192-196 °C

SMILES string

c1ccc2nc(ccc2c1)-c3ccc4ccccc4n3

InChI

1S/C18H12N2/c1-3-7-15-13(5-1)9-11-17(19-15)18-12-10-14-6-2-4-8-16(14)20-18/h1-12H

InChI key

WPTCSQBWLUUYDV-UHFFFAOYSA-N

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General description

2,2′-Biquinoline is a white crystalline solid and it melts at 176°C. It is insoluble in water, but is soluble in ethyl, amyl and isoamyl alcohol, isoamyl acetate, dimethylformamide, acetic acid, acetonitrile and carbon tetrachloride.

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Descripción
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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCM3052
BCCJ4610
BCCF3848
BCBZ4884
BCBZ3139

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The Determination of Impurities in Nuclear Grade Sodium Metal.
Silverman L.
Science, 70-71 (2013)
Analyst, 83, 299-299 (1958)
Chun-fen Zhang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 23(2), 217-220 (2003-09-10)
Steady-state fluorescence and anisotropy measurements have been used to investigate the interaction of 2,2'-biquinoline (BQ) and 1,1'-(methylenedi-1,4-phenylene)bismaleimide (MDP-BMI) with alpha-, beta-, and gamma-cyclodextrins (CDs). It was found that the reaction patterns between fluorescence molecules and CDs are remarkably different. They
Leszek Pazderski et al.
Magnetic resonance in chemistry : MRC, 45(12), 1059-1071 (2007-11-30)
1H, 13C, and 15N NMR studies of platinide(II) (M=Pd, Pt) chloride complexes with quinolines (L=quinoline-quin, or isoquinoline-isoquin; LL=2,2'-biquinoline-bquin), having the general formulae trans-/cis-[ML2Cl2] and [M(LL)Cl2], were performed and the respective chemical shifts (delta1H, delta13C, delta15N) reported. 1H coordination shifts of
Daniela Pucci et al.
Dalton transactions (Cambridge, England : 2003), 40(17), 4614-4622 (2011-04-01)
The synthesis and characterization of a series of 2,2'-biquinolines differently substituted in the 4,4'-position and their corresponding silver(I) derivatives obtained through reaction with silver triflate in a 1 : 1 stoichiometric ratio are reported. In order to perform a systematic
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