≥95%(GC) 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
N-Methylpropionamide has been used to investigate amide-induced phase separation of hexafluoro-2-propanol-water mixtures.
| Pubchem Sid | 488181992 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488181992 |
| Sonrisas canónicas | CCC(=O)NC |
| IUPAC Name | N-methylpropanamide |
| InChIKey | QJQAMHYHNCADNR-UHFFFAOYSA-N |
| INCHI | 1S/C4H9NO/c1-3-4(6)5-2/h3H2,1-2H3,(H,5,6) |
| Isómeros SMILES | CCC(=O)NC |
| WGK Alemania | 3 |
| RTECS | UE4515000 |
| Peso molecular | 87.12 |
| Reaxy-Rn | 1737640 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1737640&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 |
| Clase | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | Secondary carboxylic acid amides |
| Alternative Parents | Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Secondary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as secondary carboxylic acid amides. These are compounds containing a secondary carboxylic acid amide functional group, with the general structure RC(=O)N(R')H (R,R'=alkyl, aryl). |
| 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 |
|---|---|---|---|
 F23101134 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F23101135 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F23101136 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F23101137 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F23101139 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F2312466 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F2312468 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| F2312470 | Certificate of Analysis | Jun 20, 2023 | N159394 |
| Sensibilidad | Hygroscopic |
|---|---|
| Índice de refracción | n20/D 1.436 |
| Punto de inflamación (°F) | 222.8 °F |
| Punto de inflamación (°C) | 105°C(lit.) |
| Punto de ebullición (°C) | 146 °C |
| Punto de fusión (°C) | −43 °C |
| Peso molecular | 87.120 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 87.0684 Da |
| Monoisotopic Mass | 87.0684 Da |
| Topological Polar Surface Area | 29.100 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 51.500 |
| 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. Yang You, Anqiang Zhang, Yaling Lin. (2016) Crosslinking mechanism of supramolecular elastomers based on linear bifunctional polydimethylsiloxane oligomers. JOURNAL OF APPLIED POLYMER SCIENCE, 133 (18): [PMID:] [10.1002/app.43385] |
