Sulfisoxazole - analytical standard , CAS No.127-69-5

CAS: 127-69-5 Cat. No.: S114292 Molecular Weight: 267.3 Beilstein Registry Number: 6737262 EC Number: 204-858-9 PubChem CID: 5344
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
BRN 0263871 | Soxamide | Soxazole | Sulfisoxazol | Sulphadimethylisoxazole | UNII-740T4C525W | Alphazole | Koro-sulf | 5-Sulphanilamido-3,4-dimethyl-isoxazole | NSC-13120 | Unisulf | 5-(p-Aminobenzenesulfonamido)-3,4-dimethylisoxazole | Amidoxal | Gantris
Storage
Store at 2-8°C
Shipped In
Wet ice
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250mg
S114292-250mg
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500mg
S114292-500mg
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S114292-1g
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Why this grade

analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 53 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
BRN 0263871 | Soxamide | Soxazole | Sulfisoxazol | Sulphadimethylisoxazole | UNII-740T4C525W | Alphazole | Koro-sulf | 5-Sulphanilamido-3, 4-dimethyl-isoxazole | NSC-13120 | Unisulf | 5-(p-Aminobenzenesulfonamido)-3, 4-dimethylisoxazole | Amidoxal | Gantris
Specifications & Purity
analytical standard
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Analytical standard
Product Properties
ALogP1
Names and Identifiers
Canonical SmilesCC1=C(ON=C1C)NS(=O)(=O)C2=CC=C(C=C2)N
IUPAC Name4-amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzenesulfonamide
InChIKeyNHUHCSRWZMLRLA-UHFFFAOYSA-N
INCHI1S/C11H13N3O3S/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10/h3-6,14H,12H2,1-2H3
Isomeric SMILES CC1=C(ON=C1C)NS(=O)(=O)C2=CC=C(C=C2)N
WGK Germany 2
RTECS WO9100000
PubChem CID 5344
Molecular Weight 267.3
Beilstein 6737262

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzenesulfonamides
Intermediate Tree Nodes Not available
Direct ParentAminobenzenesulfonamides
Alternative Parents Benzenesulfonyl compounds  Aniline and substituted anilines  Organosulfonamides  Isoxazoles  Heteroaromatic compounds  Aminosulfonyl compounds  Oxacyclic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Aminobenzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Organosulfonic acid amide - Azole - Isoxazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Primary amine - Organosulfur compound - Organopnictogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
External Descriptors sulfonamide - isoxazoles - sulfonamide antibiotic
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CYP2C19 Tchem Cytochrome P450 2C19 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pneumoniae (31063 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus fumigatus (16427 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryctolagus cuniculus (11301 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Geotrichum candidum (421 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Syncephalastrum racemosum (262 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateItem
G2209214Certificate of AnalysisJan 19, 2026 S114292
G2209003Certificate of AnalysisJun 16, 2022 S114292
E1823119Certificate of AnalysisJan 25, 2022 S114292
Chemical and Physical Properties
Melt Point(°C)192-197°C
Molecular Weight267.310 g/mol
XLogP31.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count3
Exact Mass267.068 Da
Monoisotopic Mass267.068 Da
Topological Polar Surface Area107.000 Ų
Heavy Atom Count18
Formal Charge0
Complexity373.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Hao Cui, Wei Zhan, Xuan Ji, Mingye Jiang, Xiaoting Wu, Minru Huang, Chenhui Huang, Shanshan Ma.  (2023)  Removal of sulfonamide antibiotics by a sonocatalytic Fenton-like reaction: Efficiency and mechanisms.  ENVIRONMENTAL RESEARCH,      [PMID:37838205] [10.1016/j.envres.2023.117408]
2. Jia Zhao, Heng Zhang, Yang Shi, Jianhua Guo, Mengfan Luo, Peng Zhou, Yang Liu, Chuanshu He, Zhaokun Xiong, Gang Yao, Bo Lai.  (2023)  Enhanced ferrate decontamination efficiency by acetylene black: The role of ketonic groups as electron-donating sites.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125337]
3. Kai Hu, Lixin Li, Pengzhao Han, Weixia Zhu, Zhenqiang Zhang, Wenjie Zhao, Shusheng Zhang.  (2023)  Preparation and evaluation of a tryptophan based hypercrosslinked porous polymer as an efficient adsorbent for pipette tip solid-phase extraction of sulfonamides.  FOOD CHEMISTRY,      [PMID:37776656] [10.1016/j.foodchem.2023.137536]
4. Meiling Ping, Wenchao Lv, Chen Yang, Qian Chen, Zongwen Wang, Fengfu Fu.  (2023)  A Paper-Based Multicolor Colorimetric Aptasensor for the Visual Determination of Multiple Sulfonamides Based on Aptamer-Functionalized Magnetic Beads and NADH–Ascorbic Acid-Mediated Gold Nanobipyramids.  Chemosensors,  11  (7): (386).  [PMID:] [10.3390/chemosensors11070386]
5. Xu-Hui Li, Yuan-Yuan Cui, Xun Wu, Abdukader Abdukayum, Cheng-Xiong Yang.  (2023)  Fabrication of zwitterionic magnetic microporous organic network for efficient extraction of fluoroquinolone antibiotics from meat samples.  FOOD CHEMISTRY,      [PMID:37459710] [10.1016/j.foodchem.2023.136808]
6. Zongwen Wang, Xiating Li, Feng Zhang, Yu Gao, Jintian Cheng, FengFu Fu.  (2023)  Regulating the Growth Rate of Gold Nanobipyramids via a HCl-NADH-Ascorbic Acid System toward a Dual-Channel Multicolor Colorimetric Immunoassay for Simultaneously Screening and Detecting Multiple Sulfonamides.  ANALYTICAL CHEMISTRY,      [PMID:37382204] [10.1021/acs.analchem.3c01928]
7. Jia Zhao, Heng Zhang, Yang Shi, Mengfan Luo, Hongyu Zhou, Zhenjun Xie, Ye Du, Peng Zhou, Chuanshu He, Gang Yao, Bo Lai.  (2023)  Efficient activation of ferrate by Ru(III): Insights into the major reactive species and the multiple roles of Ru(III).  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:37379593] [10.1016/j.jhazmat.2023.131927]
8. Kaiyuan Luo, Yang Shi, Rongfu Huang, Xipeng Wei, Zelin Wu, Peng Zhou, Heng Zhang, Yin Wang, Zhaokun Xiong, Bo Lai.  (2023)  Activation of periodate by N-doped iron-based porous carbon for degradation of sulfisoxazole: Significance of catalyst-mediated electron transfer mechanism.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:37295335] [10.1016/j.jhazmat.2023.131790]
9. Liwei Yang, Fashan Yang, Heng Zhang, Hongyu Zhou, Mengfan Luo, Yunmei Liu, Chuanliang Zhao, Lu Zheng, Bo Lai.  (2023)  Insight into the electron transfer regime of periodate activation on MnO2: The critical role of surface Mn(IV).  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:37104949] [10.1016/j.jhazmat.2023.131479]
10. Qidi Pan, Zhe Gao, He Meng, Xianghua Guo, Meitian Zhang, Yiwei Tang.  (2023)  A Novel Sulfonamide, Molecularly Imprinted, Upconversion Fluorescence Probe Prepared by Pickering Emulsion Polymerization and Its Adsorption and Optical Sensing Performance.  MOLECULES,  28  (8): (3391).  [PMID:37110624] [10.3390/molecules28083391]
11. Xinhao Wang, Zhaokun Xiong, Hongle Shi, Zelin Wu, Bingkun Huang, Heng Zhang, Peng Zhou, Zhicheng Pan, Wen Liu, Bo Lai.  (2023)  Switching the reaction mechanisms and pollutant degradation routes through active center size-dependent Fenton-like catalysis.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2023.122569]
12. Pascaline Sanga, Juanjuan Wang, Xin Li, Jia Chen, Hongdeng Qiu.  (2023)  Effective Removal of Sulfonamides Using Recyclable MXene-Decorated Bismuth Ferrite Nanocomposites Prepared via Hydrothermal Method.  MOLECULES,  28  (4): (1541).  [PMID:36838529] [10.3390/molecules28041541]
13. Yahan Yu, Chunxiu Yu, Zelin Wu, Bingkun Huang, Peng Zhou, Heng Zhang, Wen Liu, Yucheng Liu, Zhaokun Xiong, Bo Lai.  (2023)  Switching the primary mechanism from a radical to a nonradical pathway in electrocatalytic ozonation by onsite alternating anode and cathode.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.141340]
14. Ligui Wu, Mingyu Wang, Lingling Rong, Wenbiao Wang, Linwei Chen, Qiaofeng Wu, Haoyu Sun, Xiangfeng Huang, Xiaoming Zou.  (2022)  Structural effects of sulfonamides on the proliferation dynamics of sulfonamide resistance genes in the sequencing batch reactors and the mechanism.  Journal of Environmental Sciences,      [PMID:37778792] [10.1016/j.jes.2022.11.014]
15. Zhangsong Jiang, Xiangfeng Huang, Qiaofeng Wu, Mi Li, Qili Xie, Zuwen Liu, Xiaoming Zou.  (2022)  Adsorption of sulfonamides on polyamide microplastics in an aqueous solution: behavior, structural effects, and its mechanism.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.140452]
16. Meng Xie, Mingya Yao, Shiyong Zhang, Lingshuai Kong, Lingxi Zhao, Jinhua Zhan, Ru-Song Zhao.  (2022)  Single-atom Co-N5 catalytic sites on carbon nanotubes as peroxymonosulfate activator for sulfamerazine degradation via enhanced electron transfer pathway.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2022.122398]
17. Yuhan Ning, Yixing Ye, Wanliang Liao, Yang Xu, Weiping Wang, Ai-jun Wang.  (2022)  Triazine-based porous organic polymer as pipette tip solid-phase extraction adsorbent coupled with HPLC for the determination of sulfonamide residues in food samples.  FOOD CHEMISTRY,      [PMID:35940095] [10.1016/j.foodchem.2022.133831]
18. Zhuo-Rui Jiang, Pengfei Wang, Yu-Xiao Zhou, Changhua Wang, Jiwen Jiang, Yeqing Lan, Cheng Chen.  (2022)  Fabrication of a 3D-blocky catalyst (CoMnOx@sponge) via mooring Co-Mn bimetallic oxide on sponge to activate peroxymonosulfate for convenient and efficient degradation of sulfonamide antibiotics.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.137306]
19. Mi Li, Xiaoyu Xiao, Zhangsong Jiang, Haihui Tang, Lingling Rong, Tiao Zhang, Taijia Li, Cui Hu, Ligui Wu, Xiaoming Zou.  (2021)  Metagenomic Insight into Sulfonamide-Induced Variation in Antibiotic Resistome of Soil Associated with Taxonomy, Mobile Genetic Elements (MGEs), and Function.  ACS Agricultural Science & Technology,      [PMID:] [10.1021/acsagscitech.1c00222]
20. Chenying Zhou, Peng Zhou, Minglu Sun, Yang Liu, Heng Zhang, Zhaokun Xiong, Juan Liang, Xiaoguang Duan, Bo Lai.  (2021)  Nitrogen-doped carbon nanotubes enhanced Fenton chemistry: Role of near-free iron(III) for sustainable iron(III)/iron(II) cycles.  WATER RESEARCH,      [PMID:34959068] [10.1016/j.watres.2021.117984]
21. Yu Wang, Jia Chen, Ming Guan, Hongdeng Qiu.  (2021)  Preparation of Fe/Ni Bimetallic Oxide Porous Graphene Composite Materials for Efficient Adsorption and Removal of Sulfonamides.  LANGMUIR,      [PMID:34624195] [10.1021/acs.langmuir.1c02275]
22. Qin Peige, Han Lizhen, Zhang Xiaowan, Li Mengyuan, Li Dan, Lu Minghua, Cai Zongwei.  (2021)  MIL-101(Fe)-derived magnetic porous carbon as sorbent for stir bar sorptive-dispersive microextraction of sulfonamides.  MICROCHIMICA ACTA,  188  (10): (1-11).  [PMID:34523015] [10.1007/s00604-021-04993-w]
23. Zeming Wang, Zihao Wang, Wei Li, Yeqing Lan, Cheng Chen.  (2021)  Performance comparison and mechanism investigation of Co3O4-modified different crystallographic MnO2 (α, β, γ, and δ) as an activator of peroxymonosulfate (PMS) for sulfisoxazole degradation.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.130888]
24. Houmei Liu, Pian Jin, Mi Jiang, Yu Duan, Guozheng Zhu, Hui Yu, Hongdeng Qiu.  (2021)  Performance evaluation of silica microspheres functionalized by different amine-ligands for hydrophilic interaction chromatography.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:33582513] [10.1016/j.chroma.2021.461967]
25. Mi Li, Lingling Rong, Shifan Zhou, Xiaoyu Xiao, Ligui Wu, Yuxing Fan, Conghui Lu, Xiaoming Zou.  (2020)  Dissipation of Sulfonamides in Soil Emphasizing Taxonomy and Function of Microbiomes by Metagenomic Analysis.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:33172257] [10.1021/acs.jafc.0c04496]
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