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Moligand™, ≥98%(HPLC)(T) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Conservar a 2-8°C Ships Hielo húmedo 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 13 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Introducción del producto
Los estándares secundarios farmacéuticos para su aplicación en el control de calidad ofrecen a los laboratorios farmacéuticos y a los fabricantes una alternativa cómoda y rentable a la preparación de estándares de trabajo propios
| Pubchem Sid | 504750897 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504750897 |
| Sonrisas canónicas | CCS(=O)(=O)CCN1C(=NC=C1[N+](=O)[O-])C |
| IUPAC Name | 1-(2-ethylsulfonylethyl)-2-methyl-5-nitroimidazole |
| InChIKey | HJLSLZFTEKNLFI-UHFFFAOYSA-N |
| INCHI | 1S/C8H13N3O4S/c1-3-16(14,15)5-4-10-7(2)9-6-8(10)11(12)13/h6H,3-5H2,1-2H3 |
| Isómeros SMILES | CCS(=O)(=O)CCN1C(=NC=C1[N+](=O)[O-])C |
| RTECS | NI6255000 |
| PubChem CID | 5479 |
| Peso molecular | 247.27 |
| Reaxy-Rn | 618182 |
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 | Organoheterocyclic compounds |
| Clase | Azoles |
| Subclass | Imidazoles |
| Intermediate Tree Nodes | Substituted imidazoles |
| Direct Parent | Nitroimidazoles |
| Alternative Parents | Nitroaromatic compounds 1,2,5-trisubstituted imidazoles N-substituted imidazoles Sulfones Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | 1,2,5-trisubstituted-imidazole - Nitroaromatic compound - Nitroimidazole - Trisubstituted imidazole - N-substituted imidazole - Sulfone - Heteroaromatic compound - Sulfonyl - C-nitro compound - Organic nitro compound - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organosulfur compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as nitroimidazoles. These are compounds containing an imidazole ring which bears a nitro group. |
| External Descriptors | imidazoles |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 20, 2026 | T162647 | |
| Certificate of Analysis | Mar 11, 2026 | T162647 | |
| Certificate of Analysis | Mar 11, 2026 | T162647 | |
| Certificate of Analysis | Mar 11, 2026 | T162647 | |
| Certificate of Analysis | Mar 11, 2026 | T162647 | |
| Certificate of Analysis | Mar 11, 2026 | T162647 | |
| Certificate of Analysis | May 21, 2022 | T162647 | |
| Certificate of Analysis | May 21, 2022 | T162647 | |
| Certificate of Analysis | May 21, 2022 | T162647 |
| Solubilidad | Insoluble in water; Soluble in Acetone; Slightly soluble in Methanol; Very slightly soluble in Ethanol |
|---|---|
| Punto de fusión (°C) | 129 °C |
| Peso molecular | 247.270 g/mol |
| XLogP3 | -0.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 247.063 Da |
| Monoisotopic Mass | 247.063 Da |
| Topological Polar Surface Area | 106.000 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 345.000 |
| 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. Anlin Xu, Wanqun Liu, Ziyan Yang, Liya Cao, Ignasi Sirés, Qiqi Zhang, Yongjun Zhang. (2023) Waste tire upcycling for the efficient electrogeneration of H2O2 in advanced degradation of the antibiotic tinidazole by electro-Fenton process. Journal of Cleaner Production, [PMID:] [10.1016/j.jclepro.2023.139661] |
| 2. Shaojie Wang, Yongbo Wang, Yuanna Ning, Qiming Liu. (2023) Inner filter effect-based near-infrared fluorescent probe for detection of metronidazole on a smartphone-integrated analytical platform. ANALYST, 148 (11): (2544-2552). [PMID:37144556] [10.1039/D3AN00039G] |
| 3. Zhiyong Zheng, Yuehua Deng, Weining Xie, Sirui Chen, Xiaoxiao Liang, Shiyuan Liu, Yanbin Jiang, Huaiyu Yang. (2023) Co-Former Screening Method for Multicomponent Crystals Based on Partial Least Squares Regression: A Case Study of Ciprofloxacin. CRYSTAL GROWTH & DESIGN, [PMID:] [10.1021/acs.cgd.2c01414] |
| 4. Lin Li, Yingying Li, Sijia Zhang, Ting Wang, Xiaohong Hou. (2022) Monolithic and compressible MIL-101(Cr)/cellulose aerogel/melamine sponge based microextraction in packed syringe towards trace nitroimidazoles in water samples prior to UPLC-MS/MS analysis. TALANTA, [PMID:36122434] [10.1016/j.talanta.2022.123935] |
| 5. Yang Wang, Hongwei Yuan, Ye Wan, Lei Zhang. (2022) Three-dimensional acanthosphere-like hierarchical Co@graphitic carbon for dispersive magnetic solid-phase extraction of nitroimidazole. JOURNAL OF CHROMATOGRAPHY A, [PMID:35623194] [10.1016/j.chroma.2022.463163] |
| 6. Tao Li, Liukai Zhu, Jiaheng Li, Zidan Cao, Jiao Sha, Yu Li, Baozeng Ren. (2022) Solubility, thermodynamic properties and molecular simulation of tinidazole in fourteen mono-solvents at different temperatures. JOURNAL OF CHEMICAL THERMODYNAMICS, [PMID:] [10.1016/j.jct.2022.106767] |
| 7. Yu Wang, Juanjuan Wang, Ming Guan, Parashuram Kallem, Hongdeng Qiu, Jia Chen. (2022) Bimetallic nitrogen-doped porous graphene for highly efficient magnetic solid phase extraction of 5-nitroimidazoles in environmental water. ANALYTICA CHIMICA ACTA, [PMID:35361436] [10.1016/j.aca.2022.339698] |
| 8. Tong Jianan, Zhou Huiyun, Zhou Jingjing, Chen Yawei, Shi Jing, Zhang Jieke, Liang Xinyu, Du Tianyuan. (2021) Design and evaluation of chitosan-amino acid thermosensitive hydrogel. Marine Life Science & Technology, 4 (1): (74-87). [PMID:37073351] [10.1007/s42995-021-00116-9] |
| 9. Xueqing Guo, Yang Liu, Wenjuan Dong, Qin Hu, Yong Li, Shaomin Shuang, Chuan Dong, Lishuai Cai, Xiaojuan Gong. (2021) Azithromycin detection in cells and tablets by N,S co-doped carbon quantum dots. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, [PMID:33561684] [10.1016/j.saa.2021.119506] |
| 10. Gaofeng Liang, Hao Shi, Yijun Qi, Jinghua Li, Aihua Jing, Qiwei Liu, Wenpo Feng, Guangda Li, Shegan Gao. (2020) Specific Anti-biofilm Activity of Carbon Quantum Dots by Destroying P. gingivalis Biofilm Related Genes. International Journal of Nanomedicine, [PMID:32801701] [10.2147/IJN.S253416] |
| 11. Qianqian Wang, Weihua Liu, Lin Hao, Chun Wang, Qiuhua Wu, Zhi Wang. (2020) Fabrication of magnetic porous organic framework for effective enrichment and assay of nitroimidazoles in chicken meat. FOOD CHEMISTRY, [PMID:32619936] [10.1016/j.foodchem.2020.127427] |
| 12. Guodong Ren, Xiaoyu Hou, Yu Kang, Rong Zhang, Min Zhang, Wen Liu, Lihong Li, Shuangyan Wei, Haojiang Wang, Bin Wang, Haipeng Diao. (2020) Efficient preparation of nitrogen-doped fluorescent carbon dots for highly sensitive detection of metronidazole and live cell imaging. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, [PMID:32193157] [10.1016/j.saa.2020.118251] |
| 13. Na Xu, Hong-Wei Li, Yuqing Wu. (2016) Hydrothermal synthesis of polyethylenimine-protected high luminescent Pt-nanoclusters and their application to the detection of nitroimidazoles. ANALYTICA CHIMICA ACTA, [PMID:28110684] [10.1016/j.aca.2016.12.033] |
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