Iohexol - 10mM in DMSO , Diagnostic agent, CAS No.66108-95-0, Diagnostic agent

CAS: 66108-95-0 Cat. No.: I425328 Peso molecular: 821.14 Beilstein Registry Number: 2406632 Número EC: 266-164-2
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
iohexol|66108-95-0|Omnipaque|Nycodenz|Exypaque|Iohexolum|Omnipaque 240|Omnipaque 70|Omnipaque 140|Omnipaque 180|Omnipaque 210|Omnipaque 300|Omnipaque 350|Oraltag|WIN 39424|WIN-39424|Iohexolum [INN-Latin]|CHEBI:31709|EINECS 266-164-2|BRN 2406632|N,N'-Bis(2
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
I425328-1ml
1
39,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 36 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Useful as a nonionic density gradient medium.

Specifications

Sinónimos
iohexol | 66108-95-0 | Omnipaque | Nycodenz | Exypaque | Iohexolum | Omnipaque 240 | Omnipaque 70 | Omnipaque 140 | Omnipaque 180 | Omnipaque 210 | Omnipaque 300 | Omnipaque 350 | Oraltag | WIN 39424 | WIN-39424 | Iohexolum [INN-Latin] | CHEBI:31709 | EINECS 266-164-2 | BRN 2406632 | N, N'-Bis(2
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Non-ionic monomeric triiodinated x-ray contrast agent. Density gradient medium to measure hemodynamic parameters in vivo. Induces apoptosis. Orally active.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Diagnostic agent
Propiedades del producto
ALogP-3
Nombres e identificadores
Sonrisas canónicasCC(=O)N(CC(CO)O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)C(=O)NCC(CO)O)I
IUPAC Name5-[acetyl(2,3-dihydroxypropyl)amino]-1-N,3-N-bis(2,3-dihydroxypropyl)-2,4,6-triiodobenzene-1,3-dicarboxamide
InChIKeyNTHXOOBQLCIOLC-UHFFFAOYSA-N
INCHI1S/C19H26I3N3O9/c1-8(29)25(4-11(32)7-28)17-15(21)12(18(33)23-2-9(30)5-26)14(20)13(16(17)22)19(34)24-3-10(31)6-27/h9-11,26-28,30-32H,2-7H2,1H3,(H,23,33)(H,24,34)
Isómeros SMILES CC(=O)N(CC(CO)O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)C(=O)NCC(CO)O)I
Peso molecular 821.14
Beilstein 2406632
Reaxy-Rn 2406632
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2406632&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassAnilides
Intermediate Tree Nodes Acetanilides - Haloacetanilides
Direct ParentO-haloacetanilides
Alternative Parents P-haloacetanilides  Iodobenzenes  Aryl iodides  Tertiary carboxylic acid amides  Acetamides  Secondary alcohols  Propargyl-type 1,3-dipolar organic compounds  Carboximidic acids  Primary alcohols  Organopnictogen compounds  Organonitrogen compounds  Organoiodides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents O-haloacetanilide - P-haloacetanilide - Halobenzene - Iodobenzene - Aryl halide - Aryl iodide - Acetamide - Tertiary carboxylic acid amide - Carboxamide group - Secondary alcohol - Carboximidic acid - Carboximidic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Alcohol - Organoiodide - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as o-haloacetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.
External Descriptors organoiodine compound - benzenedicarboxamide
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 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
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
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
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
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
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
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
CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA2A Tclin Adenosine A2a receptor (16305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BDKRB2 Tclin Bradykinin B2 receptor (3970 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRNA4 Tclin Neuronal acetylcholine receptor protein alpha-4 subunit (1265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MC3R Tchem Melanocortin receptor 3 (5659 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Mc4r Melanocortin receptor 4 (1205 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
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadLight sensitive
Punto de fusión (°C)180 ℃
Peso molecular821.100 g/mol
XLogP3-3.000
Hydrogen Bond Donor Count8
Hydrogen Bond Acceptor Count9
Rotatable Bond Count12
Exact Mass820.88 Da
Monoisotopic Mass820.88 Da
Topological Polar Surface Area200.000 Ų
Heavy Atom Count34
Formal Charge0
Complexity653.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count3
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Yijie Wu, Tiantian She, Yunheng Wang, Zhe Xu, Tao Huang, Qiuyi Ji, Haiou Song, Shaogui Yang, Shiyin Li, Shicheng Yan, Limin Zhang, Huan He.  (2023)  Enhancing cationic superexchange interaction via adjustive lattice distortion in cobalt-based perovskite for improved Fenton-like decontamination.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2023.123569]
2. Qiuyi Ji, Pingping Lu, Shuying Li, Yuqi Lai, Jiandong Zhu, Zhe Xu, Gancheng Zuo, Yuan Ding, Shiyin Li, Shaogui Yang, Limin Zhang, Huan He.  (2023)  Covalent bond enhanced highly stable urea perylene diimide polymer for concurrent photocatalysis-persulfate activation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.126066]
3. Tiantian She, Yijie Wu, Qiuyi Ji, Zhe Xu, Yunheng Wang, Hailong Chu, Yazi Liu, Haiou Song, Shaogui Yang, Shiyin Li, Limin Zhang, Huan He.  (2023)  Passivating surface states of graphitic carbon nitride for improved photocatalytic Fenton-like decontamination.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125193]
4. Tingting Yu, Tingting Yu, Xiang Zhong, Xiang Zhong, Qihang Yang, Qihang Yang, Chao Gao, Chao Gao, Wenyue Chen, Wenyue Chen, Xiang Liu, Xiang Liu, Zhang Liu, Zhang Liu, Tingting Zhu, Tingting Zhu, Dongyu Li, Dongyu Li, Peng Fei, Peng Fei, Zaozao Chen, Zaozao Chen, Zhongze Gu, Zhongze Gu, Dan Zhu, Dan Zhu.  (2023)  On-chip clearing for live imaging of 3D cell cultures.  Biomedical Optics Express,  14  (6): (3003-3017).  [PMID:37342722] [10.1364/BOE.489219]
5. Ning Wang, Wenxuan Li, Tiantian Du, Man Li, Qian Zhao, Mei Li, Hongbo Wang, Li Song.  (2023)  Degradation of iohexol by potassium ferrate in synthetic water and wastewater effluent: Influencing factors, kinetics, and potential intermediates.  Environmental Technology & Innovation,      [PMID:] [10.1016/j.eti.2023.103026]
6. Yang Xiao-Yan, Zhang Jin-Guo, Zhou Qiao-Mei, Yu Jie-Ni, Lu Yuan-Fei, Wang Xiao-Jie, Zhou Jia-Ping, Ding Xin-Fa, Du Yong-Zhong, Yu Ri-Sheng.  (2022)  Extracellular matrix modulating enzyme functionalized biomimetic Au nanoplatform-mediated enhanced tumor penetration and synergistic antitumor therapy for pancreatic cancer.  JOURNAL OF NANOBIOTECHNOLOGY,  20  (1): (1-24).  [PMID:36496411] [10.1186/s12951-022-01738-6]
7. Hong-Zhe Li, Kai Yang, Hu Liao, Simon Bo Lassen, Jian-Qiang Su, Xian Zhang, Li Cui, Yong-Guan Zhu.  (2022)  Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics.  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,  119  (40): (e2201473119).  [PMID:36161886] [10.1073/pnas.2201473119]
8. Yinhao Dai, Chengdu Qi, Hui Cao, Yanni Wen, Yijie Zhao, Chenmin Xu, Shaogui Yang, Huan He.  (2022)  Enhanced degradation of sulfamethoxazole by microwave-activated peracetic acid under alkaline condition: Influencing factors and mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2022.120716]
9. Cheng Xinying, Ji Qiuyi, Sun Dunyu, Zhang Jinghua, Chen Xianxian, He Huan, Li Shiyin, Yang Shaogui, Zhang Limin.  (2022)  A comparative study on adsorption behavior of iodinated X-ray contrast media iohexol and amidotrizoic acid by magnetic-activated carbon.  ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH,  29  (30): (45404-45420).  [PMID:35147873] [10.1007/s11356-022-19127-9]
10. Xie Jun, Zhou Zonglang, Ma Sihan, Luo Xian, Liu Jiajing, Wang Shengyu, Chen Yuqiang, Yan Jianghua, Luo Fanghong.  (2021)  Facile Fabrication of BiF3: Ln (Ln = Gd, Yb, Er)@PVP Nanoparticles for High-Efficiency Computed Tomography Imaging.  Nanoscale Research Letters,  16  (1): (1-10).  [PMID:34390420] [10.1186/s11671-021-03591-2]
11. Cheng Wang, Lingyun Wu, Wenxiang Li, Junhao Fei, Jiaqi Xu, Si Chen, Senxiang Yan, Xu Wang.  (2021)  An injectable double-crosslinking iodinated composite hydrogel as a potential radioprotective spacer with durable imaging function.  Journal of Materials Chemistry B,  (15): (3346-3356).  [PMID:33881426] [10.1039/D0TB02953J]
12. Wang XiuLi, Lu Yinguang, Hua Kunwei, Yang Dezhi, Yang Yaling.  (2021)  Iodine-doped carbon dots with inherent peroxidase catalytic activity for photocatalytic antibacterial and wound disinfection.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  413  (5): (1373-1382).  [PMID:33386935] [10.1007/s00216-020-03100-x]
13. Weiming Xiang, Qiuyi Ji, Chenmin Xu, Yang Guo, Yazi Liu, Dunyu Sun, Wenwu Zhou, Zhe Xu, Chengdu Qi, Shaogui Yang, Shiyin Li, Cheng Sun, Huan He.  (2020)  Accelerated photocatalytic degradation of iohexol over Co3O4/g-C3N4/Bi2O2CO3 of p-n/n-n dual heterojunction under simulated sunlight by persulfate.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2020.119847]
14. Zheng Xiaoke, Li Chenghui, He Yaqin, Wu Lan, Hou Xiandeng.  (2020)  A novel bi-modal probe based on BaHoF5 and Cu-doped QDs with enhanced CT contrast efficiency and fluorescent brightness for tumor-targeting imaging.  MICROCHIMICA ACTA,  187  (5): (1-11).  [PMID:32249330] [10.1007/s00604-020-04240-8]
15. Chen-Yan Hu, Yuan-Zhang Hou, Yi-Li Lin, Yan-Guo Deng, Shuang-Jing Hua, Yi-Fan Du, Chiu-Wen Chen, Chung-Hsin Wu.  (2019)  Investigation of iohexol degradation kinetics by using heat-activated persulfate.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.122403]
16. Chen-Yan Hu, Yuan-Zhang Hou, Yi-Li Lin, Yan-Guo Deng, Shuang-Jing Hua, Yi-Fan Du, Chiu-Wen Chen, Chung-Hsin Wu.  (2019)  Kinetics and model development of iohexol degradation during UV/H2O2 and UV/S2O82− oxidation.  CHEMOSPHERE,      [PMID:31100631] [10.1016/j.chemosphere.2019.05.012]
17. Xiaoke Zheng, Shanling Wang, Lan Wu, Xiandeng Hou.  (2018)  Microwave-assisted facile synthesis of mono-dispersed Ba/Ho co-doped nanohydroxyapatite for potential application as binary CT imaging contrast agent.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2018.05.044]
18. Li Cui, Kai Yang, Hong-Zhe Li, Han Zhang, Jian-Qiang Su, Maria Paraskevaidi, Francis L. Martin, Bin Ren, Yong-Guan Zhu.  (2018)  Functional Single-Cell Approach to Probing Nitrogen-Fixing Bacteria in Soil Communities by Resonance Raman Spectroscopy with 15N2 Labeling.  ANALYTICAL CHEMISTRY,      [PMID:29557648] [10.1021/acs.analchem.7b05080]
19. Chen-Yan Hu, Ling Xu, Yi-Li Lin, Cong Li.  (2024)  A comparative study on the degradation of iohexol and diatrizoate during UV/persulfate process: kinetics, degradation pathways and iodinated disinfection by-products.  Environmental Science-Water Research & Technology,  10  (3): (718-728).  [PMID:] [10.1039/D3EW00696D]
20. Shuohua Zhou, Weiming Xiang, Qiang Zhong, Shaogui Yang, Gancheng Zuo, Zhe Xu, Qiuyi Ji, Jijie Kong, Chenmin Xu, Bing Yang, Dunyu Sun, Yinhao Dai, Yazi Liu, Huan He, Shiyin Li.  (2024)  Activation of peroxymonosulfate (PMS) by rGO supported Co3O4 catalyst for iohexol degradation.  Desalination and Water Treatment,      [PMID:] [10.1016/j.dwt.2024.100332]
21. Miao Jiang, Pengyun Wu, Yuwei Zhang, Mengling Wang, Mingjie Zhang, Zhaoxiang Ye, Xuejun Zhang, Cai Zhang.  (2024)  Artificial Intelligence-Driven Platform: Unveiling Critical Hepatic Molecular Alterations in Hepatocellular Carcinoma Development.  Advanced Healthcare Materials,      [PMID:38657582] [10.1002/adhm.202400291]
22. Yalin Yang, Shuang Jiang, Yu Mu, Chilu Liu, Yanxing Han, Jiandong Jiang, Yuhong Wang.  (2024)  Berberine alleviated contrast-induced acute kidney injury by mitophagy-mediated NLRP3 inflammasome inactivation in a mice model.  TOXICOLOGY AND APPLIED PHARMACOLOGY,      [PMID:38705399] [10.1016/j.taap.2024.116952]
23. Chen-Yan Hu, Li-Li Hu, Zheng-Yu Dong, Xin-Yu Yang, Hao Liu, Jia-Nan Chen, Ling-Mei Gao.  (2024)  Enhanced degradation of emerging contaminants by Far-UVC photolysis of peracetic acid: Synergistic effect and mechanisms.  WATER RESEARCH,      [PMID:38909423] [10.1016/j.watres.2024.121943]
24. Naying Qi, Jia Dong, Xiaoyang Cai, Hongtao Fan, Ying Zhang, Chang Liu, Hongguo Wang, Siqi Zhang.  (2024)  Graphene-based nanomaterials for adsorption of iodinated X-ray contrast media from contaminated water: A comparative study.  CHEMOSPHERE,      [PMID:39038712] [10.1016/j.chemosphere.2024.142915]
25. Cheng Wang, Wenfeng Tan, Xionghan Feng.  (2024)  Iron (hydr)oxides-induced activation of sulfite for contaminants degradation: The critical role of structural Fe(III).  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:39018598] [10.1016/j.jhazmat.2024.135144]
26. Cheng Wang, Shuijing Zhou, Xiaoming Wang, Wenfeng Tan, Xionghan Feng.  (2024)  Photocatalytic activation of sulfite by maghemite (γ-Fe2O3) for iohexol degradation and alleviation effect of HCO3− on water acidification.  ENVIRONMENTAL POLLUTION,      [PMID:38355082] [10.1016/j.envpol.2024.123557]
27. Chen-Yan Hu, Li-Li Hu, Tian-Yang Zhang, Xin-Yu Yang, Hao Liu, Jia-Nan Chen, Ling-Mei Gao, Zheng-Yu Dong.  (2025)  Rapid oxidation of emerging contaminants by far-UVC/chlorine system: Energy efficiency and synergistic mechanism.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2025.106958]
28. Yunheng Wang, Hengle Wang, Tiantian She, Renjie Wang, Zhe Xu, Qiuyi Ji, Shaogui Yang, Limin Zhang, Huan He.  (2024)  Transition metal induced interfacial d-p orbital hybridization boosting biochar for efficient fenton-like decontamination.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.130859]
29. Mian Li, Lian-Yu Qiu, Tian-Yang Zhang, Bin Xu, Dan Yang, Ting Ye, Heng Luo.  (2025)  Comparative evaluation of UV/Fe(C2O4)33−/PS and Fe2+/PS advanced oxidation processes: degradation efficiency, mechanisms, and environmental risks.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.134736]
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