Disodium 2-[(7-amino-1-hydroxy-3-sulphonato-2-naphthyl)azo]benzoate (CHEM089416)
| Record Information | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||
| Creation Date | 2026-04-05 02:11:01 UTC | ||||||||
| Update Date | 2026-08-28 22:50:19 UTC | ||||||||
| Accession Number | CHEM089416 | ||||||||
| Identification | |||||||||
| Common Name | Disodium 2-[(7-amino-1-hydroxy-3-sulphonato-2-naphthyl)azo]benzoate | ||||||||
| Class | Small Molecule | ||||||||
| Description | Disodium 2-[(7-amino-1-hydroxy-3-sulphonato-2-naphthyl)azo]benzoate belongs to the naphthalene sulfonic acids and derivatives, a subclass of naphthalenes within the organic compounds. This benzenoid compound has the formula C17H13N3O6S and an average molecular weight of 431.33 g/mol. | ||||||||
| Contaminant Sources | Not Available | ||||||||
| Contaminant Type | Not Available | ||||||||
| Chemical Structure |  | ||||||||
| Synonyms | Not Available | ||||||||
| Chemical Formula | C17H13N3O6S | ||||||||
| Average Molecular Mass | 431.330 g/mol | ||||||||
| Monoisotopic Mass | 387.053 g/mol | ||||||||
| CAS Registry Number | 518329-26-5 | ||||||||
| IUPAC Name | 2-[(7-amino-1-hydroxy-3-sulfonaphthalen-2-yl)diazenyl]benzoic acid | ||||||||
| Traditional Name | Not Available | ||||||||
| SMILES | [Na+].[Na+].NC1=CC2=C(O)C(N=NC3=C(C=CC=C3)C([O-])=O)=C(C=C2C=C1)S([O-])(=O)=O | ||||||||
| InChI Identifier | InChI=1/C17H13N3O6S.2Na/c18-10-6-5-9-7-14(27(24,25)26)15(16(21)12(9)8-10)20-19-13-4-2-1-3-11(13)17(22)23;;/h1-8,21H,18H2,(H,22,23)(H,24,25,26);;/q;2*+1/p-2 | ||||||||
| InChI Key | JAASVAXWTKMZPV-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 | ||||||||
| Physical Properties | |||||||||
| State | Not Available | ||||||||
| Appearance | Not Available | ||||||||
| Experimental Properties |
| ||||||||
| Predicted Properties | Not Available | ||||||||
| Spectra | |||||||||
| Spectra |
| ||||||||
| Toxicity Profile | |||||||||
| 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 | ||||||||
| Concentrations | |||||||||
| Not Available | |||||||||
| External Links | |||||||||
| Identifiers | Not Available | ||||||||
| References | |||||||||
| Synthesis Reference | Not Available | ||||||||
| MSDS | Not Available | ||||||||
| General References | Not Available | ||||||||
