Determine the necessary mass, volume, or concentration for preparing a solution.
for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Oxadixyl (Standard) is the analytical standard of Oxadixyl. This product is intended for research and analytical applications. Oxadixyl is a fungicide with activity that inhibits the growth of fungi. Oxadixyl was tested during the malic fermentation of red wine, where its concentration may be affected. The biological activity of Oxadixyl helps to evaluate its effect on microorganisms during the winemaking process.
| Sonrisas canónicas | CC1=C(C(=CC=C1)C)N(C(=O)COC)N2CCOC2=O |
|---|---|
| IUPAC Name | N-(2,6-dimethylphenyl)-2-methoxy-N-(2-oxo-1,3-oxazolidin-3-yl)acetamide |
| InChIKey | UWVQIROCRJWDKL-UHFFFAOYSA-N |
| INCHI | 1S/C14H18N2O4/c1-10-5-4-6-11(2)13(10)16(12(17)9-19-3)15-7-8-20-14(15)18/h4-6H,7-9H2,1-3H3 |
| Isómeros SMILES | CC1=C(C(=CC=C1)C)N(C(=O)COC)N2CCOC2=O |
| WGK Alemania | 3 |
| RTECS | AB8131400 |
| PubChem CID | 53735 |
| Peso molecular | 278.3 |
| Beilstein | 7098783 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Anilides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Anilides |
| Alternative Parents | m-Xylenes Phenylhydrazines Oxazolidinones Organic carbonic acids and derivatives Carboxylic acid hydrazides Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Anilide - M-xylene - Xylene - Phenylhydrazine - Oxazolidinone - Oxazolidine - Carboxylic acid hydrazide - Carbonic acid derivative - Carboxylic acid derivative - Dialkyl ether - Ether - Organoheterocyclic compound - Oxacycle - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution. |
| External Descriptors | Amide fungicides |
| Punto de inflamación (°F) | >100 °C |
|---|---|
| Punto de inflamación (°C) | >100°C |
| Punto de fusión (°C) | 104-105°C |