≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | CCOC(=O)NN |
|---|---|
| IUPAC Name | ethyl N-aminocarbamate |
| InChIKey | VYSYZMNJHYOXGN-UHFFFAOYSA-N |
| INCHI | 1S/C3H8N2O2/c1-2-7-3(6)5-4/h2,4H2,1H3,(H,5,6) |
| Isomeric SMILES | CCOC(=O)NN |
| WGK Germany | 3 |
| RTECS | FE2545000 |
| Molecular Weight | 104.11 |
| Beilstein | 3,98 |
| Reaxy-Rn | 878265 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878265&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 | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Hydrazinecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Hydrazinecarboxylic acid esters |
| Alternative Parents | Organic carbonic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydrazinecarboxylic acid ester - Carbonic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as hydrazinecarboxylic acid esters. These are ester derivatives of hydrazinecarboxylic acids. |
| External Descriptors | Not available |
| Flash Point(°F) | 186°F |
|---|---|
| Flash Point(°C) | 86°C |
| Boil Point(°C) | 108-110 °C/22 mmHg |
| Melt Point(°C) | 44-47°C |
| Molecular Weight | 104.110 g/mol |
| XLogP3 | -0.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 104.059 Da |
| Monoisotopic Mass | 104.059 Da |
| Topological Polar Surface Area | 64.400 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 64.000 |
| 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. Ming He, Jing Li, Jiajing Xu, Lukun Wu, Ning Li, Shuai Zhang. (2024) Dynamic Recyclable High-Performance Epoxy Resins via Triazolinedione–Indole Click Reaction and Cation–π Interaction Synergistic Crosslinking. Polymers, 16 (13): (1900). [PMID:39000754] [10.3390/polym16131900] |
H2406544