for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Bathocuproine disulfonic acid (BCDS) is a stable Cu+chelator and BCDS-Cu+inhibits the HIV-1 wild type protease as well as a mutant HIV-1 protease lacking cysteine. It is an extracellular copper chelator.Bathocuproinedisulfonic acid disodium salt hydrate was used as chelator in electron spin resonance spin trapping technique to study free radical generation in rats with acute sodium formate poisoning. It was used as reagent for determination of Cu and Cu-protein complexes.
| Pubchem Sid | 488202189 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488202189 |
| Canonical Smiles | CC1=C(C(=C2C=CC3=C(C(=C(N=C3C2=N1)C)S(=O)(=O)[O-])C4=CC=CC=C4)C5=CC=CC=C5)S(=O)(=O)[O-].O.[Na+].[Na+] |
| IUPAC Name | disodium;2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline-3,8-disulfonate;hydrate |
| InChIKey | ZAGWMJUGRCMNGX-UHFFFAOYSA-L |
| INCHI | 1S/C26H20N2O6S2.2Na.H2O/c1-15-25(35(29,30)31)21(17-9-5-3-6-10-17)19-13-14-20-22(18-11-7-4-8-12-18)26(36(32,33)34)16(2)28-24(20)23(19)27-15;;;/h3-14H,1-2H3,(H,29,30,31)(H,32,33,34);;;1H2/q;2*+1;/p-2 |
| Isomeric SMILES | CC1=C(C(=C2C=CC3=C(C(=C(N=C3C2=N1)C)S(=O)(=O)[O-])C4=CC=CC=C4)C5=CC=CC=C5)S(=O)(=O)[O-].O.[Na+].[Na+] |
| WGK Germany | 3 |
| PubChem CID | 71306850 |
| Molecular Weight | 564.54 (anhydrous basis) |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Quinolines and derivatives |
| Subclass | Phenylquinolines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylquinolines |
| Alternative Parents | Phenanthrolines Phenylpyridines Arylsulfonic acids and derivatives Methylpyridines Benzene and substituted derivatives Sulfonyls Organosulfonic acids Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phenylquinoline - 1,10-phenanthroline - 4-phenylpyridine - Arylsulfonic acid or derivatives - Methylpyridine - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Azacycle - Organic alkali metal salt - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic salt - Organic sodium salt - Organic cation - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 D2623241 | Certificate of Analysis | Mar 11, 2026 | B486593 |
| D2623242 | Certificate of Analysis | Mar 11, 2026 | B486593 |
| F2309241 | Certificate of Analysis | Mar 11, 2026 | B486593 |
| F2309244 | Certificate of Analysis | Mar 11, 2026 | B486593 |
| I2512249 | Certificate of Analysis | Aug 23, 2025 | B486593 |
| I2512250 | Certificate of Analysis | Aug 23, 2025 | B486593 |
| C2504410 | Certificate of Analysis | Feb 22, 2025 | B486593 |
| C2504411 | Certificate of Analysis | Feb 22, 2025 | B486593 |
| C2414332 | Certificate of Analysis | Feb 24, 2024 | B486593 |
| C2414333 | Certificate of Analysis | Feb 24, 2024 | B486593 |
| C2414334 | Certificate of Analysis | Feb 24, 2024 | B486593 |
| C2414335 | Certificate of Analysis | Feb 24, 2024 | B486593 |
| F2309240 | Certificate of Analysis | Apr 10, 2023 | B486593 |
| F2309242 | Certificate of Analysis | Apr 10, 2023 | B486593 |
| Molecular Weight | 582.600 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 2 |
| Exact Mass | 582.051 Da |
| Monoisotopic Mass | 582.051 Da |
| Topological Polar Surface Area | 158.000 Ų |
| Heavy Atom Count | 39 |
| Formal Charge | 0 |
| Complexity | 874.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 4 |
| 1. Wu Haibin, Liu Shoupei, Chen Sen, Qin Changlu, Yan Wenjiao, Cao Xiangting, Zhou Yongjian, Duan Yuyou. (2026) Generation of proliferative hESC-derived grape-clustered hepatocyte organoids with multipolar architecture as regenerative counterpart via synergy of YAP and IGF2 pathways. Cell Death & Disease, [PMID:] [10.1038/s41419-026-08635-y] |
