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14335

Sigma-Aldrich

2,2′-Biquinoline-4,4′-dicarboxylic acid

≥90% (TLC)

Synonym(s):

2,2′-Bicinchoninic acid

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About This Item

Empirical Formula (Hill Notation):
C20H12N2O4
CAS Number:
Molecular Weight:
344.32
Beilstein/REAXYS Number:
321561
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.25

Quality Level

assay

≥90% (TLC)

form

powder

storage temp.

2-8°C

SMILES string

OC(=O)c1cc(nc2ccccc12)-c3cc(C(O)=O)c4ccccc4n3

InChI

1S/C20H12N2O4/c23-19(24)13-9-17(21-15-7-3-1-5-11(13)15)18-10-14(20(25)26)12-6-2-4-8-16(12)22-18/h1-10H,(H,23,24)(H,25,26)

InChI key

AFYNADDZULBEJA-UHFFFAOYSA-N

Application

2,2′-Biquinoline-4,4′-dicarboxylic acid has been used in a study that synthesized and structurally characterized six metal-organic coordination polymers.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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C Faye et al.
Analytical biochemistry, 420(2), 147-154 (2011-10-11)
The efficient immobilization of antibodies on monolithic support is one of the most critical steps when preparing immunoaffinity supports. In this work, the ADECA (amino density estimation by colorimetric assay) method was adapted to tridimensional supports (in a dynamic mode)
Randall I Krohn
Current protocols in cell biology, Appendix 3, 3H-3H (2011-09-08)
Protein quantification is an important step for handling protein samples for isolation and characterization; it is a prerequisite step before submitting proteins for chromatographic, electrophoretic, or immunochemical analysis and separation. Colorimetric methods are fast, simple, and not laborious. This unit
Baoyan Bai et al.
Proteomics, 12(19-20), 3044-3048 (2012-08-15)
Efficient extraction and accurate quantification of nucleolar macromolecules are critical for in vitro analysis, especially for studying RNA, DNA, and protein dynamics under identical conditions. There is presently no single method that efficiently and simultaneously isolates these three macromolecular constituents
Erik H Christen et al.
Organic & biomolecular chemistry, 10(33), 6629-6632 (2012-07-24)
The Cu(I)-catalyzed cycloaddition of terminal azides and alkynes (click chemistry) represents a highly specific reaction for the functionalization of biomolecules with chemical moieties such as dyes or polymer matrices. In this study we evaluate the use of bicinchoninic acid (BCA)
C Petrella et al.
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society, 22(11), 1248-1256 (2010-07-28)
Cannabinoids (CBs) evoke their effects by activating the cannabinoid receptor subtypes CB1-r and CB2-r and exert anti-inflammatory effects altering chemokine and cytokine expression. Various cytokines and chemokines are produced and released by rodent pancreatic acini in acute pancreatitis. Although CB1-r

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