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Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Armazenar a 2-8°C, carregado com árgon Ships Gelo húmido 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 24 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504752181 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504752181 |
| Sorrisos canónicos | CNC(=O)N |
| IUPAC Name | methylurea |
| InChIKey | XGEGHDBEHXKFPX-UHFFFAOYSA-N |
| INCHI | 1S/C2H6N2O/c1-4-2(3)5/h1H3,(H3,3,4,5) |
| SMILES isoméricas | CNC(=O)N |
| WGK Alemanha | 3 |
| RTECS | YT7175000 |
| CAS alternativo | 598-50-5,608090-15-9 |
| Termos de entrada MeSH | methylurea;monomethylurea |
| Peso molecular | 74.08 |
| Beilstein | 878189 |
| Reaxy-Rn | 878189 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878189&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 |
| Classe | Organic carbonic acids and derivatives |
| Subclass | Ureas |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Ureas |
| Alternative Parents | Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Urea - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as ureas. These are compounds containing two amine groups joined by a carbonyl (C=O) functional group. |
| External Descriptors | ureas |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 17, 2026 | M107951 | |
| Certificate of Analysis | Jun 17, 2026 | M107951 | |
| Certificate of Analysis | Apr 28, 2025 | M107951 | |
| Certificate of Analysis | Apr 28, 2025 | M107951 | |
| Certificate of Analysis | Aug 02, 2024 | M107951 | |
| Certificate of Analysis | Aug 02, 2024 | M107951 | |
| Certificate of Analysis | Aug 02, 2024 | M107951 | |
| Certificate of Analysis | Jul 01, 2024 | M107951 | |
| Certificate of Analysis | Jul 01, 2024 | M107951 | |
| Certificate of Analysis | Jul 01, 2024 | M107951 | |
| Certificate of Analysis | Jul 01, 2024 | M107951 | |
| Certificate of Analysis | Jan 03, 2023 | M107951 | |
| Certificate of Analysis | Jan 03, 2023 | M107951 | |
| Certificate of Analysis | Jan 03, 2023 | M107951 | |
| Certificate of Analysis | Jan 03, 2023 | M107951 | |
| Certificate of Analysis | Jan 03, 2023 | M107951 | |
| Certificate of Analysis | Dec 12, 2022 | M107951 | |
| Certificate of Analysis | Jun 30, 2022 | M107951 | |
| Certificate of Analysis | Jun 10, 2021 | M107951 |
| Solubilidade | Solubility in water: Completely soluble; Very soluble in Methanol; Insoluble in Ether |
|---|---|
| Sensibilidade | heat sensitive;Air sensitive;Hygroscopic |
| Ponto de fusão (°C) | 99°C |
| Peso molecular | 74.080 g/mol |
| XLogP3 | -1.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 74.048 Da |
| Monoisotopic Mass | 74.048 Da |
| Topological Polar Surface Area | 55.100 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 42.900 |
| 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. Yuan Zhang, Lu Yu, Wuxia Ge, Wentao Bi, David Da Yong Chen. (2023) Preparation of carbon-rich material from Dendrobium officinale polysaccharide in deep eutectic system. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:37832618] [10.1016/j.ijbiomac.2023.127394] |
| 2. Xinjin Yu, Zhimei Zhao, Xiaoli Yan, Jianhua Xie, Qiang Yu, Yi Chen. (2023) Extraction optimization of tea saponins from Camellia oleifera seed meal with deep eutectic solvents: Composition identification and properties evaluation. FOOD CHEMISTRY, [PMID:37392622] [10.1016/j.foodchem.2023.136681] |
| 3. Ying Zhang, Jian Ye, Yinzhi Jiang, Shuqin Jiang, Wei Xiao, Dongchu Wei. (2023) Alkylaluminum/Urea Hybrid Cocatalysts and Their Use in Iron-Catalyzed Oligomerization of Ethylene. Macromolecular Reaction Engineering, 17 (3): (2300013). [PMID:] [10.1002/mren.202300013] |
| 4. Wei Wang, Baian Pu, Chi Ma, Chengxiang Shi, Lun Pan, Xiangwen Zhang, Ji-Jun Zou. (2023) Pd/C catalytic cyclopropanation of polycyclic olefins for synthesis of high-energy-density strained fuels. AICHE JOURNAL, 69 (7): (e18085). [PMID:] [10.1002/aic.18085] |
| 5. Ziwei Ju, Jiaxuan Fan, Zilin Meng, Runhua Lu, Haixiang Gao, Wenfeng Zhou. (2022) A high-throughput semi-automated dispersive liquid–liquid microextraction based on deep eutectic solvent for the determination of neonicotinoid pesticides in edible oils. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2022.108193] |
| 6. Dan Cao, Min Liu, Yung-Chih Su, Zehui Yang, Wentao Bi, David Da Yong Chen. (2022) Adsorption behavior of anthraquinones in deep eutectic solvent on polyester fiber and its application. Sustainable Chemistry and Pharmacy, [PMID:] [10.1016/j.scp.2022.100680] |
| 7. Yinghui Bian, Weichuan Jiang, Yonglei Zhang, Lishun Zhao, Xiaohang Wang, Zichuan Lv, Shuai Zhou, Yuqing Han, Hui Chen, Meng-Chang Lin. (2021) Understanding the Oxidation and Reduction Reactions of Sulfur in Rechargeable Aluminum-Sulfur Batteries with Deep Eutectic Solvent and Ionic Liquid Electrolytes. ChemSusChem, 15 (1): (e202101398). [PMID:34532988] [10.1002/cssc.202101398] |
| 8. Hongyan Wang, Song Ma, Zhimao Zhou, Minjie Li, Hui Wang. (2020) Alkylation of isobutane with butene catalyzed by deep eutectic ionic liquids. FUEL, [PMID:] [10.1016/j.fuel.2020.117419] |
| 9. Zheng-Meng Jiang, Lan-Jin Wang, Zhao Gao, Bo Zhuang, Qiang Yin, E-Hu Liu. (2018) Green and efficient extraction of different types of bioactive alkaloids using deep eutectic solvents. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2018.10.057] |
| 10. Jiaqin Wang, Yanying Zhou, Man Wang, Wentao Bi, Hongli Li, David Da Yong Chen. (2018) High-Throughput Analysis for Artemisinins with Deep Eutectic Solvents Mechanochemical Extraction and Direct Analysis in Real Time Mass Spectrometry. ANALYTICAL CHEMISTRY, [PMID:29381342] [10.1021/acs.analchem.7b04060] |
| 11. Bo Zhuang, Li-Li Dou, Ping Li, E-Hu Liu. (2016) Deep eutectic solvents as green media for extraction of flavonoid glycosides and aglycones from Platycladi Cacumen. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, [PMID:27915199] [10.1016/j.jpba.2016.11.049] |
| 12. Li Duan, Li-Li Dou, Long Guo, Ping Li, E-Hu Liu. (2016) Comprehensive Evaluation of Deep Eutectic Solvents in Extraction of Bioactive Natural Products. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.6b00091] |
| 13. Xiaohua Zhao, Xiang Liu, Ming Lu. (2014) β-cyclodextrin-capped palladium nanoparticle-catalyzed ligand-free Suzuki and Heck couplings in low-melting β-cyclodextrin/NMU mixtures. APPLIED ORGANOMETALLIC CHEMISTRY, 28 (8): (635-640). [PMID:] [10.1002/aoc.3173] |
| 14. Han-Qing Pang, Jia-Xiu Guo, Yang Yang, Chuan Jiang, Xuan-Hao Zhang, Wei Shi, Chun-Yang Bi, Bing-Chun Yan. (2024) Development of deep eutectic solvents for the efficient extraction of active compounds and removal of hepatotoxic compounds from Polygonum multiflorum Thunb.. JOURNAL OF MOLECULAR LIQUIDS, [PMID:] [10.1016/j.molliq.2024.125591] |
| 15. Guanfeng Deng, Pingjin Li, Heng Liang, Tao Chen, Lijun Zhou, Hongyu Yang, Xiaoyu Jiang, Chunbang Ding, Shiling Feng. (2025) Extraction of polysaccharides from Camellia oleifera leaves by dual enzymes combined with deep eutectic solvents screened by ANN and COSMO-RS. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:39961566] [10.1016/j.ijbiomac.2025.141131] |
| 16. Si-wei Rao, Feng-xiang Zhang, Yuan-yuan Duan, Zi-hao Chen, Dong Liang, Wei Shi. (2024) Urea-based deep eutectic solvents enzyme system for high efficiency extraction of alkaloids and flavonoids in plants: Zanthoxylum nitidum (Roxb.) DC. as a case. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2024.109964] |
| 17. Zhenqian Wei, Weiyan Zhang, Menghao Du, Haiyan Zhong, Xuezhi Fang. (2024) Widely targeted metabolomic and KEGG analyses of natural deep eutectic solvent-based saponins extraction from Camellia oleifera Abel.: Effects on composition. FOOD CHEMISTRY, [PMID:38636384] [10.1016/j.foodchem.2024.139333] |
| 18. Wentao Zheng, Jialing Chen, Yujiao Jia, Nengqi Sun, Xiankun Wu. (2025) Thermodynamic analysis of nitric oxide absorption in deep eutectic solvents comprising 1,1,3,3-tetramethylguanidine. JOURNAL OF CHEMICAL THERMODYNAMICS, [PMID:] [10.1016/j.jct.2025.107563] |
| 19. Xinyue Zhang, Yuan Yao, Yingying Cao, Xin Tan, Xiaomin Fang, Yanqiang Zhang. (2025) Enhanced Cyclopropanation of Norbornene as a High-Energy Fuel by Pd Single-Site Catalysts. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.5c01267] |
| 20. Fuhui Luo, Fenfen Zeng, Zhongqiao Zhao, Xu Ren, Yong He, Xia Yang, Fengxiang Zhang, Hanqing Pang, Wei Shi. (2025) A Novel Green and Efficient Strategy for Natural Products by Extraction with Acidic Electrolytic Oxidation Water-Assisted Deep Eutectic Solvent. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.5c03706] |
| 21. Guanfeng Deng, Heng Liang, Qilu Xue, Tao Chen, Lijun Zhou, Ming Yuan, Chunbang Ding, Shiling Feng. (2025) Tailor-Made Deep Eutectic Solvents Designed via COSMO-RS for Enhanced Polyphenol Extraction from Lethariella cladonioides. Journal of Future Foods, [PMID:] [10.1016/j.jfutfo.2025.06.024] |
| 22. Yao Yuan, Zhang Xinyue, Cao Yingying, Liu Long, Zhang Yanqiang, Zhang Suojiang. (2025) Strain engineering of single-site Cu on SWCNTs for highly efficient diene cyclopropanation. Nature Communications, [PMID:41402267] [10.1038/s41467-025-66241-6] |
| 23. Xiaojun Bao, Yu Cao, Lei Gong, Renjiang Li, Dongshun Deng. (2026) Separation of Taurine and Na2SO4 Using in Situ Formation of Deep Eutectic Solvents: Experiments and Computation Simulation. NEW JOURNAL OF CHEMISTRY, [PMID:] [10.1039/D5NJ04739K] |
| 24. Yonghui Guo, Ruyu Yan, Yaya Jia, Yiming Yang, Zihan You, Xiaoyan Zhang, Shan Liu. (2026) Dual-mode interfacial regulation by a bifunctional additive for stable zinc anodes. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:] [10.1016/j.jcis.2026.141361] |
| 25. Yangyang Zhang, Weifeng Jin, Tianxue Chen, Jin Han, Li Yu, Haitong Wan, Haofang Wan. (2026) Experiment-confirmed machine learning optimization of NADES extraction with ultrasound assistance and Mendelian randomization evidence on antioxidant effects of ferulic acid and ligustilide from Angelicae Sinensis Radix. ULTRASONICS SONOCHEMISTRY, [PMID:] [10.1016/j.ultsonch.2026.108000] |
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