≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Ammelide can be synthesized via hydrolysis of 2-amino-4,6-dichloro-s-triazine in the presence of acid or base or by the reaction between urea and cyanogen iodide at 130-140 degrees.
AMMC is demethylated by Human CYP2D6 to the fluorescent product 3-[2-(N,N-diethyl-N-methy
| Pubchem Sid | 528769151 |
|---|---|
| Sorrisos canónicos | C1(=NC(=O)NC(=O)N1)N |
| IUPAC Name | 6-amino-1H-1,3,5-triazine-2,4-dione |
| InChIKey | YSKUZVBSHIWEFK-UHFFFAOYSA-N |
| INCHI | 1S/C3H4N4O2/c4-1-5-2(8)7-3(9)6-1/h(H4,4,5,6,7,8,9) |
| SMILES isoméricas | C1(=NC(=O)NC(=O)N1)N |
| WGK Alemanha | 3 |
| Peso molecular | 128.09 |
| Reaxy-Rn | 126963 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=126963&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 | Organoheterocyclic compounds |
| Classe | Triazines |
| Subclass | Triazinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Triazinones |
| Alternative Parents | Aminotriazines 1,3,5-triazines Heteroaromatic compounds Ureas Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Amino-1,3,5-triazine - Aminotriazine - Triazinone - 1,3,5-triazine - Heteroaromatic compound - Urea - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as triazinones. These are compounds containing a triazine ring which bears a ketone group a carbon atom. |
| External Descriptors | dihydroxy-1,3,5-triazine - monoamino-1,3,5-triazine |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Item |
|---|---|---|---|
 F2117092 | Certificate of Analysis | Sep 22, 2026 | A134713 |
| F2117094 | Certificate of Analysis | Sep 22, 2026 | A134713 |
| F2328199 | Certificate of Analysis | Apr 07, 2025 | A134713 |
| F2328205 | Certificate of Analysis | Apr 07, 2025 | A134713 |
| D2027049 | Certificate of Analysis | Feb 15, 2022 | A134713 |
| Sensibilidade | Moisture sensitive |
|---|---|
| Peso molecular | 128.090 g/mol |
| XLogP3 | -1.500 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 128.033 Da |
| Monoisotopic Mass | 128.033 Da |
| Topological Polar Surface Area | 96.600 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 196.000 |
| 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 |
| 1. Chong Xia, Yuanqing Zhu, Song Zhou, Yongming Feng, Jie Shi. (2023) Catalytic elimination potential and kinetic model of urea and its by-products on V2O5-WO3/TiO2 catalyst. FUEL, [PMID:] [10.1016/j.fuel.2023.130573] |
| 2. Hailiang Yang, Qian Chen, Yuankui Huang, Yaoping Hu. (2025) Carbon nitride quantum dots with full-color room-temperature phosphorescence via in situ precursor engineering and rigid matrix confinement. CARBON, [PMID:] [10.1016/j.carbon.2025.121074] |
