Determine the necessary mass, volume, or concentration for preparing a solution.
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2mM 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 41 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Cephalexin Hydrate is a semi-synthetic, cephalosporin antibiotic. it is a first generation cephalosporin. The compound is most effective against gram positive cocci and has moderate activity against some gram negative bacilli.
| Canonical Smiles | CC1=C(N2C(C(C2=O)NC(=O)C(C3=CC=CC=C3)N)SC1)C(=O)O |
|---|---|
| IUPAC Name | (6R,7R)-7-[[(2R)-2-amino-2-phenylacetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| InChIKey | ZAIPMKNFIOOWCQ-UEKVPHQBSA-N |
| INCHI | 1S/C16H17N3O4S/c1-8-7-24-15-11(14(21)19(15)12(8)16(22)23)18-13(20)10(17)9-5-3-2-4-6-9/h2-6,10-11,15H,7,17H2,1H3,(H,18,20)(H,22,23)/t10-,11-,15-/m1/s1 |
| Isomeric SMILES | CC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)SC1)C(=O)O |
| Molecular Weight | 347.38 |
| Reaxy-Rn | 630107 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=630107&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 |
| Class | Lactams |
| Subclass | Beta lactams |
| Intermediate Tree Nodes | Cephems |
| Direct Parent | Cephalosporins |
| Alternative Parents | N-acyl-alpha amino acids and derivatives Alpha amino acid amides Phenylacetamides Aralkylamines 1,3-thiazines Tertiary carboxylic acid amides Secondary carboxylic acid amides Amino acids Azetidines Thiohemiaminal derivatives Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Cephalosporin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Phenylacetamide - Aralkylamine - Meta-thiazine - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Amino acid or derivatives - Amino acid - Carboxamide group - Azetidine - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Thioether - Hemithioaminal - Dialkylthioether - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Amine - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as cephalosporins. These are compounds containing a 1,2-thiazine fused to a 2-azetidinone to for a oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid moiety or a derivative thereof. |
| External Descriptors | cephalosporin |
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| Melt Point(°C) | >161°C |
|---|---|
| Molecular Weight | 347.400 g/mol |
| XLogP3 | 0.600 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 347.094 Da |
| Monoisotopic Mass | 347.094 Da |
| Topological Polar Surface Area | 138.000 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 600.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| 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 |
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| 30. Zhenbin Chen, Haohan Cai, Feng Huang, Zongping Wang, Yiqun Chen, Zizheng Liu, Pengchao Xie. (2024) Degradation of β-lactam antibiotics by Fe(III)/HSO3− system and their quantitative structure-activity relationship. ENVIRONMENTAL RESEARCH, [PMID:38986801] [10.1016/j.envres.2024.119577] |
| 31. Yang Zhitao, Wang Shan, Wang Shijie, Han Sijia, Wei Lingzui, Yang Wenlong. (2024) Detection of doxycycline by using a tapered droplet structure fiber sensor. REVIEW OF SCIENTIFIC INSTRUMENTS, 95 (3): [PMID:38477656] [10.1063/5.0164105] |
| 32. Wei Jiang, Run-Han Yan, Ru-Ping Liang, Jian-Ding Qiu. (2024) Double-lanthanide functionalized covalent organic framework hybrid material for the enhanced adsorption of fluoroquinolone antibiotics via synergistic effect. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2024.130753] |
| 33. Rilong Liu, Hangzhen Lan, Song Yan, Lu Huang, Daodong Pan, Yichun Wu. (2024) Penicillin binding proteins-based immunoassay for the selective and quantitative determination of beta-lactam antibiotics. ENZYME AND MICROBIAL TECHNOLOGY, [PMID:39241682] [10.1016/j.enzmictec.2024.110507] |
| 34. Senwei Jiang, Hangzhen Lan, Daodong Pan, Lu Huang, Yichun Wu. (2024) Penicillin-Binding Proteins and Graphene/Chitosan Nanocomposite-Based Electrochemical Assay for Multiple Beta-Lactam Antibiotics Detection in Milk. International Journal of Electrochemistry, 2024 (1): (1463794). [PMID:] [10.1155/2024/1463794] |
| 35. Shengxi Zhai, Mengyuan Bai, Fengling Yue, Haifang Wang, Jingcheng Huang, Haowei Dong, Bei Yuan, Zhengtao Li, Pengwei Zhang, Mingxin Zhao, Yemin Guo, Xia Sun, WenPing Zhao. (2024) Strip biosensors based on broad-spectrum aptamers and cationic polymers for the on-site rapid detection of tetracycline antibiotics residues in milk. FOOD CHEMISTRY, [PMID:39467503] [10.1016/j.foodchem.2024.141743] |
| 36. Linqian Hou, Qiulan Li, Jitao Li, Dezhi Yang, Yaling Yang. (2025) Cu,Fe,B/Cur-CDs with peroxidase- and ascorbic acid oxidase-like catalytic activity for dual-signal fluorescence sensing of metronidazole. FOOD CHEMISTRY, [PMID:40774207] [10.1016/j.foodchem.2025.145757] |
| 37. Xiaofei Fu, Chenyang Zhu, Jitao Yan, Xinru Lu, Zuming He, Yongmei Xia, Wenqian Lian, Qiangshun Wu, Jiali Chen, Jiameng Pu, Tinghai Yang, Yong Gao. (2025) “Three-in-one”: Triple-engineered charge transfer in Bi4O5Br2/FeS2 hybrid for efficient treatment of cefalexin and real pharmaceutical wastewater. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.168514] |
| 38. Yilin Wu, Jian Lu, Xinyu Lin, Jia Gao, Li Chen, Jiuyun Cui, Peng Lv, Xinlin Liu, Minjia Meng, Yongsheng Yan. (2018) Bioinspired Synthesis of Janus Nanocomposite-Incorporated Molecularly Imprinted Membranes for Selective Adsorption and Separation Applications. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.8b01442] |
| 39. Chunyan Zhao, Jiangdong Dai, Zhiping Zhou, Xiaohui Dai, Yongli Zou, Ping Yu, Tianbian Zou, Chunxiang Li, Yongsheng Yan. (2013) One-pot method for obtaining hydrophilic tetracycline-imprinted particles via precipitation polymerization in ethanol. JOURNAL OF APPLIED POLYMER SCIENCE, 131 (7): [PMID:] [10.1002/app.40071] |
| 40. Yulin Chen, Danying Xing, Yang Sui, Zexin Liu, Xiaodan Zhao. (2025) Efficacy and mechanism of peracetic acid activation with CuFeS2 to degrade tetracycline: Synergy of copper and iron species. Journal of Water Process Engineering, [PMID:] [10.1016/j.jwpe.2025.107042] |
| 41. 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] |