Determine the necessary mass, volume, or concentration for preparing a solution.
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≥80% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged Ships Normal 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Usually used in fabrication of high performance electrode of supercapacitor based on chemically modified graphene hydrogel.And also used in preparation of ordered assemblies of organic and biological molecules on gold surfaces.
| Sorrisi canonici | C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)N |
|---|---|
| IUPAC Name | 2-aminoanthracene-9,10-dione |
| InChIKey | XOGPDSATLSAZEK-UHFFFAOYSA-N |
| INCHI | 1S/C14H9NO2/c15-8-5-6-11-12(7-8)14(17)10-4-2-1-3-9(10)13(11)16/h1-7H,15H2 |
| Isomeri SMILES | C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)N |
| WGK Germania | 3 |
| RTECS | CB5120000 |
| Peso molecolare | 223.23 |
| Beilstein | 745903 |
| Reaxy-Rn | 745903 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=745903&ln= |
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 | Benzenoids |
| Classe | Anthracenes |
| Subclass | Anthraquinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 2-aminoanthraquinones |
| Alternative Parents | Aryl ketones Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | 2-aminoanthraquinone - Aryl ketone - Ketone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homopolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as 2-aminoanthraquinones. These are organic compounds containing an anthraquinone ring system, which is substituted at the 2-position by an amino group. |
| External Descriptors | anthraquinone |
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| Solubilità | Soluble in Dimethylformamide |
|---|---|
| Sensibilità | Air sensitive |
| Punto di infiammabilità (°F) | 541°F |
| Punto di infiammabilità (°C) | 283℃ |
| Punto di fusione (°C) | 302°C |
| Peso molecolare | 223.230 g/mol |
| XLogP3 | 2.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 223.063 Da |
| Monoisotopic Mass | 223.063 Da |
| Topological Polar Surface Area | 60.200 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 352.000 |
| 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 | 1 |