≥90% 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Formic hydrazide was used in the synthesis of 1,2,4-triazole derivatives. It was also used in the synthesis of new anticancer agent, 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(β-D-glucopyranosyl)-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazole-5,7(6H)-dione
| Sonrisas canónicas | C(=O)NN |
|---|---|
| IUPAC Name | formohydrazide |
| InChIKey | XZBIXDPGRMLSTC-UHFFFAOYSA-N |
| INCHI | 1S/CH4N2O/c2-3-1-4/h1H,2H2,(H,3,4) |
| Isómeros SMILES | C(=O)NN |
| WGK Alemania | 3 |
| RTECS | LQ8615000 |
| Peso molecular | 60.06 |
| Beilstein | 635759 |
| Reaxy-Rn | 635759 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635759&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 | Not available |
| Direct Parent | Carboxylic acid hydrazides |
| Alternative Parents | Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carboxylic acid hydrazide - 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 carboxylic acid hydrazides. These are carboxylic acid derivatives containing a carbonyl group in which the carbon is directly linked to a hydrazide group (N-N). |
| 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 |
|---|---|---|---|
 F2526351 | Certificate of Analysis | Jul 15, 2024 | F109757 |
| K1920219 | Certificate of Analysis | Sep 08, 2023 | F109757 |
| C2302554 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| C2302555 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| C2302556 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| C2302831 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| D2617098 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| L2426210 | Certificate of Analysis | Jan 04, 2023 | F109757 |
| E1810047 | Certificate of Analysis | Mar 31, 2022 | F109757 |
| Solubilidad | Soluble in water, ethanol and acetone. |
|---|---|
| Sensibilidad | heat & Moisture sensitive |
| Punto de inflamación (°F) | 233.6 °F |
| Punto de inflamación (°C) | 112℃ |
| Punto de ebullición (°C) | 90 °C/0.7 mmHg |
| Punto de fusión (°C) | 52-57°C |
| Peso molecular | 60.056 g/mol |
| XLogP3 | -2.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 60.0324 Da |
| Monoisotopic Mass | 60.0324 Da |
| Topological Polar Surface Area | 55.100 Ų |
| Heavy Atom Count | 4 |
| Formal Charge | 0 |
| Complexity | 20.000 |
| 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. Jingyi Zhang, Zidan Cao, Di Fan, Yu Li, Tao Li, Baozeng Ren. (2023) Solid-liquid phase equilibrium of adiphenine hydrochloride in twelve pure solvents. JOURNAL OF CHEMICAL THERMODYNAMICS, [PMID:] [10.1016/j.jct.2023.107067] |
| 2. Jianhang Qi, Jiale Liu, Yongming Ma, Yanjie Cheng, Kai Chen, Wenjing Hu, Junwei Xiang, Xiaoru Wang, Jianwei Zhao, Yang Zhou, Anyi Mei, Hongwei Han. (2024) Modulating Dual Functionalities of Hydrazide Derivatives for Iodide Oxidation Suppression and Defect Passivation in Printable Mesoscopic Perovskite Solar Cells. Advanced Energy Materials, [PMID:] [10.1002/aenm.202402344] |
| 3. Pengshuai Zhang, Haiyan Luo, Lan Cui, Jixiu Deng, Shiyu Xie, Danfeng Liu, Shuqi Wang, Xiaoying Si, Zichao Wang, Yameng Wan, En Zhang, Xing Li, Lu Zhang. (2022) Assessment of solid–liquid equilibrium behavior and thermodynamic analysis of natural plant extracts artemisinin (Form I) in twelve mono-solvents. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2022.120975] |
