Determine the necessary mass, volume, or concentration for preparing a solution.
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10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs 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 36 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| ALogP | -0.2 |
|---|
| Sonrisas canónicas | CCN1C=C(C(=O)C2=CC(=C(N=C21)N3CCNCC3)F)C(=O)O |
|---|---|
| IUPAC Name | 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,8-naphthyridine-3-carboxylic acid |
| InChIKey | IDYZIJYBMGIQMJ-UHFFFAOYSA-N |
| INCHI | 1S/C15H17FN4O3/c1-2-19-8-10(15(22)23)12(21)9-7-11(16)14(18-13(9)19)20-5-3-17-4-6-20/h7-8,17H,2-6H2,1H3,(H,22,23) |
| Isómeros SMILES | CCN1C=C(C(=O)C2=CC(=C(N=C21)N3CCNCC3)F)C(=O)O |
| Peso molecular | 320.32 |
| Reaxy-Rn | 3628995 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3628995&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 | Organoheterocyclic compounds |
| Clase | Diazanaphthalenes |
| Subclass | Naphthyridines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthyridine carboxylic acids and derivatives |
| Alternative Parents | Pyridinylpiperazines N-arylpiperazines Fluoroquinolones Pyridinecarboxylic acids Dialkylarylamines Aminopyridines and derivatives Aryl fluorides Imidolactams Vinylogous amides Heteroaromatic compounds Amino acids Azacyclic compounds Carboxylic acids Dialkylamines Monocarboxylic acids and derivatives Organooxygen compounds Organofluorides Organic oxides Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Naphthyridine carboxylic acid - Fluoroquinolone - N-arylpiperazine - Pyridinylpiperazine - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Dialkylarylamine - Aminopyridine - Aryl fluoride - Aryl halide - 1,4-diazinane - Piperazine - Imidolactam - Pyridine - Heteroaromatic compound - Vinylogous amide - Amino acid or derivatives - Amino acid - Azacycle - Secondary amine - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Organic oxide - Organohalogen compound - Organofluoride - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as naphthyridine carboxylic acids and derivatives. These are compounds containing a naphthyridine moiety, where one of the ring atoms bears a carboxylic acid group. |
| External Descriptors | N-arylpiperazine - monocarboxylic acid - amino acid - 1,8-naphthyridine derivative - quinolone antibiotic - fluoroquinolone antibiotic |
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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 | May 13, 2026 | E425763 |
| Peso molecular | 320.320 g/mol |
|---|---|
| XLogP3 | -0.200 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 3 |
| Exact Mass | 320.128 Da |
| Monoisotopic Mass | 320.128 Da |
| Topological Polar Surface Area | 85.800 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 521.000 |
| 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. Huizhu Zhang, Yimin Tang, Weie Wang, Dongxue Yu, Libin Yang, Xin Jiang, Wei Song, Bing Zhao. (2023) A new semiconductor heterojunction SERS substrate for ultra-sensitive detection of antibiotic residues in egg. FOOD CHEMISTRY, [PMID:37603998] [10.1016/j.foodchem.2023.137163] |
| 2. Ye Jiang, Xiaochan Wang, Guo Zhao, Yinyan Shi, Yao Wu. (2023) In-situ SERS detection of quinolone antibiotic residues in aquaculture water by multifunctional Fe3O4@mTiO2@Ag nanoparticles. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, [PMID:37385202] [10.1016/j.saa.2023.123056] |
| 3. Panxue Wang, Li Wang, Cen Li, Xiang Li, Guoliang Li. (2022) Reliable and Rapid Detection and Quantification of Enrofloxacin Using a Ratiometric SERS Aptasensor. MOLECULES, 27 (24): (8764). [PMID:36557895] [10.3390/molecules27248764] |
| 4. Wang Jiarui, Feng Juanjuan, Sun Min, Lian Yujing, Wang Minglin, Qiao Luqin. (2022) Sulfonic acid-functionalized covalent organic frameworks as the coating for stir bar sorptive extraction of fluoroquinolones in milk samples. MICROCHIMICA ACTA, 190 (1): (1-9). [PMID:36469152] [10.1007/s00604-022-05534-9] |
| 5. Lishan Zhang, Zujie Yao, Huamei Tang, Qingli Song, Huanhuan Song, Jindong Yao, Zhen Li, Xiaofang Xie, Yuexu Lin, Xiangmin Lin. (2022) The Lysine Acetylation Modification in the Porin Aha1 of Aeromonas hydrophila Regulates the Uptake of Multidrug Antibiotics. MOLECULAR & CELLULAR PROTEOMICS, 21 (9): [PMID:35605723] [10.1016/j.mcpro.2022.100248] |
| 6. Yangjie LI, Jiaying HUANG, Jihui FANG, Zhiye HUANG. (2022) [Fast screening and confirmation of 73 common prohibited compounds in cosmetics by ultra performance liquid chromatography-quadrupole-time-of-flight high resolution mass spectrometry].. Chinese Journal of Chromatography, 40 (5): (433-442). [PMID:35478002] [10.3724/sp.j.1123.2021.09010] |
| 7. Faguang Ma, Yan Yan, Zhixin Yu, Yilin Wu, Xinlin Liu. (2020) Freestanding flexible molecularly imprinted nanocomposite membranes for selective separation applications: an imitated core–shell PEI@SiO2-based MIM design. NEW JOURNAL OF CHEMISTRY, 44 (44): (19091-19102). [PMID:] [10.1039/D0NJ03489D] |
| 8. Weie Wang, Qinqin Sang, Ming Yang, Juan Du, Libin Yang, Xin Jiang, Xiaoxia Han, Bing Zhao. (2019) Detection of several quinolone antibiotic residues in water based on Ag-TiO2 SERS strategy. SCIENCE OF THE TOTAL ENVIRONMENT, [PMID:31710852] [10.1016/j.scitotenv.2019.134956] |
| 9. Zhenping Liu, Mingliang Jin, Han Lu, Jiyuan Yao, Xin Wang, Guofu Zhou, Lingling Shui. (2019) Molecularly imprinted polymer decorated 3D-framework of functionalized multi-walled carbon nanotubes for ultrasensitive electrochemical sensing of Norfloxacin in pharmaceutical formulations and rat plasma. SENSORS AND ACTUATORS B-CHEMICAL, [PMID:] [10.1016/j.snb.2019.02.097] |
| 10. Jia Gao, Shi Zhou, Zhiqiang Hou, Qi Zhang, Minjia Meng, Chunxiang Li, Yilin Wu, Yongsheng Yan. (2019) One pot-economical fabrication of molecularly imprinted membrane employing carbon nanospheres sol coagulation bath with specific separation and advanced antifouling performances. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2019.01.079] |
| 11. Hua Jianhao, Jiao Yang, Wang Meng, Yang Yaling. (2018) Determination of norfloxacin or ciprofloxacin by carbon dots fluorescence enhancement using magnetic nanoparticles as adsorbent. MICROCHIMICA ACTA, 185 (2): (1-9). [PMID:29594473] [10.1007/s00604-018-2685-x] |
| 12. Qiong Yang, Xuanping Tan, Jidong Yang. (2015) Sensitive determination of enoxacin in pharmaceutical formulations by its quench effect on the fluorescence of glutathione-capped CdTe quantum dots. LUMINESCENCE, 31 (1): (241-246). [PMID:26105709] [10.1002/bio.2952] |
| 13. Dan Liu, Jiutong Ma, Yan Jin, Xiqian Li, Xiao Zhou, Qiong Jia, Weihong Zhou. (2014) Preparation of a monolith functionalized with zinc oxide nanoparticles and its application in the enrichment of fluoroquinolone antibiotics. JOURNAL OF SEPARATION SCIENCE, 38 (1): (134-140). [PMID:25354394] [10.1002/jssc.201400893] |
| 14. Xin Jiang, Kaiwei Li, Yimin Tang, Xiuwen Wang, Wei Kan, Libin Yang, Bing Zhao. (2024) A double defects-dominated flexible TiO2 matrix for in-situ SERS sensing of antibiotic residues in aquatic ecosystem (fish & fishpond water) and their on-site degradation in flowing water. SCIENCE OF THE TOTAL ENVIRONMENT, [PMID:38387568] [10.1016/j.scitotenv.2024.171154] |
| 15. Li Kaiwei, Jiang Han, Wang Liying, Wang Rui, Zhang Xuewei, Yang Libin, Jiang Xin, Song Wei, Zhao Bing. (2024) A flexible semiconductor SERS substrate by in situ growth of tightly aligned TiO2 for in situ detection of antibiotic residues. MICROCHIMICA ACTA, 191 (2): (1-11). [PMID:38286863] [10.1007/s00604-024-06193-8] |
| 16. Kaigang An, Xin Li, Jia Chen, Shuang Zhang, Jing Xiao, Qing Wang, Hongdeng Qiu. (2024) Deep eutectic solvent-assisted synthesis of La–Ce hybrid nanorods for the colorimetric determination of tetracycline in foods. Analytical Methods, 16 (22): (3551-3561). [PMID:38780040] [10.1039/D4AY00412D] |
| 17. Yuanchuan Ren, Yan Hu, Nanqi Ren, Xiaojuan Su, Fenghui Wu, Dandan Chen, Xuejun Zhu, Qiang Niu, Yan Guo. (2024) Electrochemical assisted single atom copper modified novel nitrogen doped porous carbon mediated catalytic activity based on D-band center modification: Rapid degradation of enoxacin. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2024.130854] |
| 18. Xiuzhen Wei, Zelong Chen, Liangliang Xu, Yue Li, Xuekang Zhang, Xianghao Zhang, Qinghua Zhou, Meilan Pan. (2024) Engineering Brønsted acid sites for enhanced nonradical pathways in antibiotic contaminant degradation. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2024.157225] |
| 19. Wenrui Li, Yike Dang, Ruihong Wang, Weizhong Jin, Xiangli Chen, Yafei Zhai, Zhuoqun Su, Guoliang Li. (2024) Fabrication of magnetic functionalized layered double hydroxide nanomaterials for detecting trace fluoroquinolones residues in meat integrated with HPLC-MS/MS. JOURNAL OF FOOD COMPOSITION AND ANALYSIS, [PMID:] [10.1016/j.jfca.2024.106672] |
| 20. Gaoshuang Hu, Ziyang Liu, Yiqin Zhang, Tao Zhao, Zhuqing Xing, Shan Gao, Jianxiong Hao. (2024) Quantum dot-based biomimetic fluorescence immunoassays for enrofloxacin detection in animal-derived foods. Analytical Methods, [PMID:39545783] [10.1039/D4AY01753F] |
| 21. Yin-Xia Sun, Xue Bai, Ai-Ping Luo, Yu Sun, Zhe-Peng Deng, Wan-Hong Sun, Wen-Yu Han. (2025) Ratiometric fluorescent sensor CQDx@Co/Mn-MOF for rapid and sensitive detection of quinolone antibiotics. TALANTA, [PMID:40179685] [10.1016/j.talanta.2025.128034] |
| 22. Jie Wu, Yuanjie Qin, Xiaoxin Mei, Lin Cai, Wen Hao, Guozhen Fang. (2025) Self-Enhanced Near-Infrared Copper Nanoscale Electrochemiluminescence Probe for the Sensitive Detection of Ciprofloxacin in Foods. Foods, 14 (3): (538). [PMID:39942131] [10.3390/foods14030538] |
| 23. Tianci Lv, Fubin Liu, Mengqian Xiao, Ying Liu, Litao Wang, Guihua Gao. (2024) Synthesis of reusable hierarchical Pore PVDF-MIL-101(Cr) foam for Solid phase extraction of fluoroquinolones from water and its adsorption behavior for anionic and cationic dyes. JOURNAL OF CHROMATOGRAPHY A, [PMID:39637615] [10.1016/j.chroma.2024.465577] |
| 24. Yanning Zheng, Dankui Liao, Bimei Xie, Jinlei Sun, Jianhua Sun, Zhangfa Tong, Guangzhi Zhou. (2024) Tuning the heterostructure improves the catalytic activity of recyclable nanozymes for efficient absorption and degradation of norfloxacin-contaminated water. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2024.126576] |
| 25. Jia Jia, Qian Liu, Tao Wang, Borui Zou, Xiong Xiong, Jun Xu, Chenxi Wu. (2025) Multiple stressors enhance Microcystis dominance and modulate phycospheric antibiotic resistome in aquatic mesocosm. JOURNAL OF HAZARDOUS MATERIALS, [PMID:40865219] [10.1016/j.jhazmat.2025.139633] |
| 26. Mantang Chen, Shucai Gao, Ruihong Liu, Xiaoyu Wang, Cong Nie, Fuwei Xie, Haidong Gao, Libin Wan. (2025) Imprinted metal-organic framework for selective extraction and determination of fluoroquinolone antibiotics in food samples. LWT-FOOD SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.lwt.2025.117743] |
| 27. Guangxin Yang, Jingru Zhang, Junyu Zhang, Peng Wang, Wei Xia, Jun Wang, Xiaosheng Shen, Cong Kong. (2025) Utilization of wolfberry biomass waste-derived biochar as an efficient solid-phase extraction material for antibiotic detection in aquatic products. FOOD CHEMISTRY, [PMID:40617214] [10.1016/j.foodchem.2025.145390] |
| 28. Jiaxuan Liu, Wensi Ma, Xinyue Huang, Lei Jiang, Lin Yuan, Xiuling Ji, Yujiao Tu. (2025) Rapeseed oil residue-based fluorescent probes for bifunctional detection of Hg2+ and aureomycin hydrochloride. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2025.114165] |
| 29. Shuanghuan Gu, Sen Wang, Yongju Zhang, Zhixiang Xu, Longhua Xu. (2025) A ternary AuNP/NiFe-LDH/MWCNT heterostructure enhanced electrochemical biomimetic sensor for sensitive detection of enrofloxacin in aquatic foods. FOOD CHEMISTRY, [PMID:41205465] [10.1016/j.foodchem.2025.146940] |
| 30. Jinzheng Zhang, Xiaoyu Lei, Jiajing Tang, Qing Zhao, Li Li, Jinlun Feng, Yubao Li, Yi Zuo. (2025) Moisture-Tolerant Polyurethane-Based Bone Cement Containing Enoxacin for the Sex-Specific Repair of Osteoporotic Defects. JOURNAL OF APPLIED POLYMER SCIENCE, [PMID:] [10.1002/app.58080] |
| 31. Jing Xu, Si-Heng Luo, Chen-ru Xiong, Jia-hao Liu, Zeyu Zhao, Wei-qi Lin, Wei Zhang, Ping Guo, Cheng Pan, Quanlong Li, Zhong-Qun Tian, Bin Ren, Guo-Kun Liu. (2025) AI-Enhanced Rapid SERS Screening of Trace Quinolone Antibiotics across the Source-Pathway-Sink Ecosystem. ANALYTICAL CHEMISTRY, [PMID:41263298] [10.1021/acs.analchem.5c05040] |
| 32. Wang Xugang, Zhang Chenxi, Yang Chengjie, Guo Xiaotong, Hu Siyun, Qian Chaonan, Liao Bingrui, Ashraf Usama, Jin Weiwei, Yang Fei, Ouyang Hehao, Liu Yixin, Chen Huanchun, Huang Qiuying, Si Youhui, Zhu Bibo, Cao Shengbo, Ye Jing. (2026) Secretory NS1’ protein of orthoflavivirus promotes viral transmission to mosquitoes by suppressing the RNAi pathway. Science China-Life Sciences, [PMID:41535661] [10.1007/s11427-025-3071-4] |
| 33. Jinli Lin, Xueying Wu, Fangkai Du, Lirong Jiang. (2026) Smartphone-assisted ratiometric fluorescence sensing platform based on Eu-DES@hydrogel for visual quantitative detection of levofloxacin in milk and honey. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2026.117172] |
| 34. Yi Jintao, Fu Nani, Zhong Wenhui, Liu Xia, Zhou Anqi, Li Xun. (2026) A CQDs-doped europium-DPA framework for fluorescence and colorimetric dual-mode sensing of amoxicillin and ciprofloxacin. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, [PMID:41718751] [10.1007/s00216-026-06405-5] |
| 35. Wang Yanbin, Wang Liling. (2026) Sulfur-doped iron-based nanoenzymes as excellent peroxidase mimics for norfloxacin detection and array-based recognition of quinolone antibiotics. MICROCHIMICA ACTA, 193 (4): (284). [PMID:] [10.1007/s00604-026-07999-4] |
| 36. Cong Yan, Ruyi Li, Ding Yang, Mingchuan Yu, Cong Liu, Hui Li, Yufei Zhou. (2026) Precise thermal regulation of defect and coordination structures in carbon nitride govern divergent photocatalytic activities. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:] [10.1016/j.jcis.2026.140390] |