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35020

Supelco

2,2′-Biquinoline

for spectrophotometric det. of Cu, ≥99.0%

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Synonym(s):
2,2′-Diquinolyl, Cuproin
Empirical Formula (Hill Notation):
C18H12N2
CAS Number:
119-91-5
Molecular Weight:
256.30
Beilstein:
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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WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The Determination of Impurities in Nuclear Grade Sodium Metal.
Silverman L.
Science, 70-71 (2013)
J Chowdhury et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(11), 2107-2115 (2000-11-01)
Surface enhanced Raman scattering (SERS) in silver sol and normal Raman spectra in the bulk and in solution of 2,2' biquinoline (BQ) molecule have been investigated. The observed Raman bands along with their corresponding FTIR bands have been assigned based
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
Analyst, 83, 299-299 (1958)
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
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