≥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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | CCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1 |
|---|---|
| IUPAC Name | N-phenyloctadecanamide |
| InChIKey | ZOLJFBQEKSZVCB-UHFFFAOYSA-N |
| INCHI | 1S/C24H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(26)25-23-20-17-16-18-21-23/h16-18,20-21H,2-15,19,22H2,1H3,(H,25,26) |
| Isomeric SMILES | CCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1 |
| PubChem CID | 69476 |
| Molecular Weight | 359.6 |
| Reaxy-Rn | 2660029 |
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 | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Anilides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Anilides |
| Alternative Parents | N-arylamides Fatty amides Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Anilide - N-arylamide - Fatty amide - Fatty acyl - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Aromatic homomonocyclic compound |
| Description | 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 | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 C2528644 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| C2528645 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| C2528646 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| C2528647 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| C2528648 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| C2528649 | Certificate of Analysis | Oct 14, 2024 | S161126 |
| Boil Point(°C) | 154°C/10mmHg(lit.) |
|---|---|
| Melt Point(°C) | 94 °C |
| Molecular Weight | 359.600 g/mol |
| XLogP3 | 9.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 17 |
| Exact Mass | 359.319 Da |
| Monoisotopic Mass | 359.319 Da |
| Topological Polar Surface Area | 29.100 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 309.000 |
| 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 |
