≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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.
| Pubchem Sid | 488184302 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184302 |
| Canonical Smiles | CC(=O)NCO |
| IUPAC Name | N-(hydroxymethyl)acetamide |
| InChIKey | HWJHZLJIIWOTGZ-UHFFFAOYSA-N |
| INCHI | 1S/C3H7NO2/c1-3(6)4-2-5/h5H,2H2,1H3,(H,4,6) |
| Isomeric SMILES | CC(=O)NCO |
| RTECS | AC3610000 |
| Molecular Weight | 89.09 |
| Beilstein | 2(4)405 |
| Reaxy-Rn | 506226 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506226&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 | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | Acetamides |
| Alternative Parents | Secondary carboxylic acid amides Alkanolamines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acetamide - Secondary carboxylic acid amide - Alkanolamine - 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 acetamides. These are organic compounds with the general formula RNHC(=O)CH3, where R= organyl group. |
| 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 |
|---|---|---|---|
 G2528479 | Certificate of Analysis | Jul 29, 2025 | A151630 |
| G2522171 | Certificate of Analysis | Jul 25, 2025 | A151630 |
| G2522173 | Certificate of Analysis | Jul 25, 2025 | A151630 |
| G2522214 | Certificate of Analysis | Jul 25, 2025 | A151630 |
| G2312148 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312152 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312153 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312154 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312159 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312160 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312164 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| G2312611 | Certificate of Analysis | Jul 21, 2023 | A151630 |
| Solubility | Solubility in water: Completely soluble; Very soluble in Alcohol; Soluble in Chloroform; Insoluble in Ether |
|---|---|
| Sensitivity | Moisture sensitive. |
| Melt Point(°C) | 52 °C |
| Molecular Weight | 89.090 g/mol |
| XLogP3 | -1.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 89.0477 Da |
| Monoisotopic Mass | 89.0477 Da |
| Topological Polar Surface Area | 49.300 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 52.800 |
| 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. Mian Hu, Jiayi Zheng, Zhiheng Ye, Yufan Jin, Xinyu Pan, Jiahui Huang, Yage Zhang, Junliang Wang, Zhong-Ting Hu, Zhiyan Pan. (2025) Subcritical catalytic water oxidation for conversion DMAC waste carbon resources to acetic acid. Journal of Environmental Chemical Engineering, [PMID:] [10.1016/j.jece.2025.115965] |
