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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.
| Sonrisas canónicas | C1CCCCCC(=O)NCCCCC1 |
|---|---|
| IUPAC Name | azacyclotridecan-2-one |
| InChIKey | JHWNWJKBPDFINM-UHFFFAOYSA-N |
| INCHI | 1S/C12H23NO/c14-12-10-8-6-4-2-1-3-5-7-9-11-13-12/h1-11H2,(H,13,14) |
| Isómeros SMILES | C1CCCCCC(=O)NCCCCC1 |
| WGK Alemania | 1 |
| RTECS | CL6940000 |
| Peso molecular | 197.32 |
| Beilstein | 122031 |
| Reaxy-Rn | 122031 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=122031&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Clase | Macrolactams |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Macrolactams |
| Alternative Parents | Secondary carboxylic acid amides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Macrolactam - Carboxamide group - Lactam - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Mar 12, 2024 | O159931 | |
| Certificate of Analysis | Feb 27, 2024 | O159931 | |
| Certificate of Analysis | Jan 19, 2024 | O159931 | |
| Certificate of Analysis | Aug 28, 2023 | O159931 | |
| Certificate of Analysis | Aug 28, 2023 | O159931 | |
| Certificate of Analysis | Dec 14, 2022 | O159931 | |
| Certificate of Analysis | Jul 21, 2022 | O159931 | |
| Certificate of Analysis | Jul 21, 2022 | O159931 | |
| Certificate of Analysis | Jul 21, 2022 | O159931 | |
| Certificate of Analysis | Jul 21, 2022 | O159931 |
| Punto de inflamación (°F) | 383 °F |
|---|---|
| Punto de inflamación (°C) | 195 °C |
| Punto de fusión (°C) | 152 °C |
| Peso molecular | 197.320 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 197.178 Da |
| Monoisotopic Mass | 197.178 Da |
| Topological Polar Surface Area | 29.100 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 156.000 |
| 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 |