≥99% 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
N.N'-Bis(2-hydroxyethyl)oxamide is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
| Pubchem Sid | 488184956 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184956 |
| Canonical Smiles | C(CO)NC(=O)C(=O)NCCO |
| IUPAC Name | N,N'-bis(2-hydroxyethyl)oxamide |
| InChIKey | FPQJEXTVQZHURJ-UHFFFAOYSA-N |
| INCHI | 1S/C6H12N2O4/c9-3-1-7-5(11)6(12)8-2-4-10/h9-10H,1-4H2,(H,7,11)(H,8,12) |
| Isomeric SMILES | C(CO)NC(=O)C(=O)NCCO |
| WGK Germany | 3 |
| Molecular Weight | 176.17 |
| Beilstein | 4(4)1541 |
| Reaxy-Rn | 1778350 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1778350&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 | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Alpha amino acid amides |
| Alternative Parents | N-acylethanolamines Secondary carboxylic acid amides Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-amino acid amide - N-acylethanolamine - Carboxamide group - Secondary carboxylic acid amide - Alkanolamine - Alcohol - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. |
| 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 |
|---|---|---|---|
 H1408086 | Certificate of Analysis | Mar 20, 2026 | B122646 |
| B2222328 | Certificate of Analysis | Dec 10, 2025 | B122646 |
| C1412061 | Certificate of Analysis | Oct 13, 2025 | B122646 |
| C2531107 | Certificate of Analysis | Mar 15, 2025 | B122646 |
| C2531264 | Certificate of Analysis | Mar 15, 2025 | B122646 |
| C2531265 | Certificate of Analysis | Mar 15, 2025 | B122646 |
| B2222317 | Certificate of Analysis | Dec 23, 2021 | B122646 |
| C2314468 | Certificate of Analysis | Dec 23, 2021 | B122646 |
| E2326216 | Certificate of Analysis | Dec 23, 2021 | B122646 |
| F2411077 | Certificate of Analysis | Dec 23, 2021 | B122646 |
| Solubility | Insoluble in water |
|---|---|
| Sensitivity | Moisture sensitive |
| Melt Point(°C) | 169°C |
| Molecular Weight | 176.170 g/mol |
| XLogP3 | -2.100 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 176.08 Da |
| Monoisotopic Mass | 176.08 Da |
| Topological Polar Surface Area | 98.700 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 142.000 |
| 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. Zhen Huang, Shimin Geng, Yizhen Chen, Ying Li, Mingen Fei, Renhui Qiu, Tingting Chen, Wendi Liu. (2025) Biobased comb polyurethane hot-melt adhesives consisting of dangling fatty acid chains and H-bonds for tailoring bonding strength. EUROPEAN POLYMER JOURNAL, [PMID:] [10.1016/j.eurpolymj.2025.113880] |
| 2. Yi Yang, Ruixue Li, Chentong Gao, Ziwei Qin, Hao-Yang Mi, Binbin Dong, Xin Jing, Chuntai Liu, Changyu Shen. (2024) Impact-resistant, high-toughness, self-healable elastomers with physical-chemical dual-crosslinking networks for efficient energy absorption. Applied Materials Today, [PMID:] [10.1016/j.apmt.2024.102522] |
| 3. Hao Wu, Zhou Lu, Ming Jin, Junhao Xie, Jinqiu Tao, Chengjun Yue, LEI DONG, Qianping Ran. (2025) Nature-inspired Dynamic Nanoconfinement Empowers Life-like Mechanical Adaptability and Robust Environmental Resilience in Polyurethane-urea Elastomers. Journal of Materials Chemistry A, [PMID:] [10.1039/D5TA04445F] |
