≥98% 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.
Cyanoacetamide is the starting reagent for vitamin B6 synthesis.It reacts with reducing carbohydrates in borate buffer to give intense fluorescence andis useful for the automated analysis of carbohydrates as borate complexes.
Cyanoacetamide was used in spectrofluorimetric method for the determination of some antihistaminic H1 receptor antagonist drugs such as ebastine, cetirizine dihydrochloride and fexofenadine hydrochloride. It may be used in fluorometric determination of 3,4-dihydroxyphenylalanine. It was used as post column fluorigenic derivatizing agent for the bio-analysis and pharmacokinetics of chitosan ester in rabbit serum.
| Pubchem Sid | 488180602 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488180602 |
| Sonrisas canónicas | C(C#N)C(=O)N |
| IUPAC Name | 2-cyanoacetamide |
| InChIKey | DGJMPUGMZIKDRO-UHFFFAOYSA-N |
| INCHI | 1S/C3H4N2O/c4-2-1-3(5)6/h1H2,(H2,5,6) |
| Isómeros SMILES | C(C#N)C(=O)N |
| WGK Alemania | 2 |
| RTECS | AB5950000 |
| Número ONU | 3439 |
| Peso molecular | 84.08 |
| Beilstein | 878221 |
| Reaxy-Rn | 878221 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878221&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 | Primary carboxylic acid amides |
| Alternative Parents | Nitriles Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Primary carboxylic acid amide - Nitrile - Carbonitrile - 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 primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. |
| 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 |
|---|---|---|---|
 G2418291 | Certificate of Analysis | May 08, 2026 | C101310 |
| G2405168 | Certificate of Analysis | Apr 03, 2026 | C101310 |
| I2209199 | Certificate of Analysis | Mar 11, 2026 | C101310 |
| I2209198 | Certificate of Analysis | Mar 11, 2026 | C101310 |
| I2209197 | Certificate of Analysis | Mar 11, 2026 | C101310 |
| I2209196 | Certificate of Analysis | Mar 11, 2026 | C101310 |
| B2223241 | Certificate of Analysis | Sep 09, 2025 | C101310 |
| H2511046 | Certificate of Analysis | Aug 21, 2025 | C101310 |
| J2316015 | Certificate of Analysis | Jul 14, 2025 | C101310 |
| I2320082 | Certificate of Analysis | Jul 10, 2025 | C101310 |
| C2012048 | Certificate of Analysis | Jul 09, 2025 | C101310 |
| F2302906 | Certificate of Analysis | Mar 05, 2025 | C101310 |
| D2324100 | Certificate of Analysis | Feb 07, 2025 | C101310 |
| C2320589 | Certificate of Analysis | Jan 09, 2025 | C101310 |
| B2306879 | Certificate of Analysis | Nov 15, 2024 | C101310 |
| G2422557 | Certificate of Analysis | Apr 27, 2024 | C101310 |
| G2405169 | Certificate of Analysis | Apr 26, 2024 | C101310 |
| B2223253 | Certificate of Analysis | Dec 25, 2023 | C101310 |
| K2129379 | Certificate of Analysis | Sep 21, 2023 | C101310 |
| B2223289 | Certificate of Analysis | Dec 14, 2021 | C101310 |
| B2223280 | Certificate of Analysis | Dec 14, 2021 | C101310 |
| B2223250 | Certificate of Analysis | Dec 14, 2021 | C101310 |
| Solubilidad | Slightly soluble in water, soluble in ethanol. |
|---|---|
| Punto de inflamación (°F) | 419 °F |
| Punto de inflamación (°C) | 215 °C |
| Punto de fusión (°C) | 119-121°C |
| Peso molecular | 84.080 g/mol |
| XLogP3 | -1.000 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 84.0324 Da |
| Monoisotopic Mass | 84.0324 Da |
| Topological Polar Surface Area | 66.900 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 98.600 |
| 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. Le Lu, Weifang Zuo, Cuicui Wang, Cuixia Li, Tian Feng, Xi Li, Chao Wang, Yuxin Yao, Zongying Zhang, Xuesen Chen. (2021) Analysis of the postharvest storage characteristics of the new red-fleshed apple cultivar ‘meihong’. FOOD CHEMISTRY, [PMID:33752117] [10.1016/j.foodchem.2021.129470] |
| 2. Li Wang, Shengxian Liu, Wenjing Du, Tongyi Dou, Changhai Liang. (2020) High Regioselectivity Production of 5-Cyanovaleramide from Adiponitrile by a Novel Nitrile Hydratase Derived from Rhodococcus erythropolis CCM2595. ACS Omega, [PMID:32743216] [10.1021/acsomega.0c02188] |
| 3. Fei Pang, Mingyuan He, Jianping Ge. (2015) Controlled Synthesis of Fe3O4/ZIF-8 Nanoparticles for Magnetically Separable Nanocatalysts. CHEMISTRY-A EUROPEAN JOURNAL, 21 (18): (6879-6887). [PMID:25766136] [10.1002/chem.201405921] |
