
Disodium 2,2'-carbonylbis(5-methoxy-4-sulfophenolate) (CHEM111461)
| Record Information | |||||||||
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| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 22:54:22 UTC | ||||||||
| Update Date | 2026-04-05 22:54:22 UTC | ||||||||
| Accession Number | CHEM111461 | ||||||||
| Identification | |||||||||
| Common Name | Disodium 2,2'-carbonylbis(5-methoxy-4-sulfophenolate) | ||||||||
| Class | Small Molecule | ||||||||
| Description | Disodium 2,2'-carbonylbis(5-methoxy-4-sulfophenolate) is an organic compound with the formula C15H12Na2O11S2 and an average molecular weight of 478.35 g/mol. Disodium 2,2'-carbonylbis(5-methoxy-4-sulfophenolate) belongs to the benzophenones, a subclass of benzene and substituted derivatives within the organic compounds. This compound is categorized as a benzenoid. It has been identified in or released from one recorded source: electrical and electronic equipment, specifically antennas. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure | |||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C15H12Na2O11S2 | ||||||||
| Average Molecular Mass | 478.350 g/mol | ||||||||
| Monoisotopic Mass | 477.962 g/mol | ||||||||
| CAS Registry Number | Not Available | ||||||||
| IUPAC Name | Disodium 2,2'-carbonylbis(5-methoxy-4-sulfophenolate) | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | [Na+].[Na+].COC1=C(C=C(C(=O)C2=CC(=C(OC)C=C2[O-])S(O)(=O)=O)C([O-])=C1)S(O)(=O)=O | ||||||||
| InChI Identifier | InChI=1/C15H14O11S2.2Na/c1-25-11-5-9(16)7(3-13(11)27(19,20)21)15(18)8-4-14(28(22,23)24)12(26-2)6-10(8)17;;/h3-6,16-17H,1-2H3,(H,19,20,21)(H,22,23,24);;/q;2*+1/p-2 | ||||||||
| InChI Key | QDCHWIWENYCPIL-UHFFFAOYSA-L | ||||||||
| Chemical Taxonomy | |||||||||
| Classification | Not classified | ||||||||
| Biological Properties | |||||||||
| Status | Detected and Not Quantified | ||||||||
| Origin | Not Available | ||||||||
| Cellular Locations | Not Available | ||||||||
| Biofluid Locations | Not Available | ||||||||
| Tissue Locations | Not Available | ||||||||
| Pathways | Not Available | ||||||||
| Applications | Not Available | ||||||||
| Biological Roles | Not Available | ||||||||
| Chemical Roles | Not Available | ||||||||
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| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
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| Predicted Properties | Not Available | ||||||||
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| Route of Exposure | Not Available | ||||||||
| Mechanism of Toxicity | Not Available | ||||||||
| Metabolism | Not Available | ||||||||
| Toxicity Values | Not Available | ||||||||
| Lethal Dose | Not Available | ||||||||
| Carcinogenicity (IARC Classification) | Not Available | ||||||||
| Uses/Sources | Not Available | ||||||||
| Minimum Risk Level | Not Available | ||||||||
| Health Effects | Not Available | ||||||||
| Symptoms | Not Available | ||||||||
| Treatment | Not Available | ||||||||
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| Identifiers | Not Available | ||||||||
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| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||