4-Aminopyridine - ≥98% , Voltage-gated potassium channel blocker, CAS No.504-24-5, Voltage-gated potassium channel blocker

CAS: 504-24-5 Cat. No.: A113920 Molecular Weight: 94.11 Beilstein Registry Number: 105782 EC Number: 207-987-9
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
AI3-52547 | Amaya | Avitrol | Dalfampridine (USAN) | Fampridine-PR | BH3B64OKL9 | DTXCID003870 | p-amino pyridine | BRN 0105782 | gamma-Aminopyridine | C5H6N2 | pyridin-4-amine | SMR000058211 | 4 Aminopyridine | 4- Aminopyridine | DALFAMPRIDINE [USP-RS] |
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice,FedEx DG Service
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
A113920-5g
7
$9.90
25g
A113920-25g
6

$15.90

$24.90
Save $9.00 (36.14%)
100g
A113920-100g
3

$47.90

$75.90
Save $28.00 (36.89%)
250g
A113920-250g
1

$92.90

$149.90
Save $57.00 (38.03%)
500g
A113920-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$148.90

$235.90
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice,FedEx DG Service 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 67 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

4-Aminopyridine (4-AP) can be used as a:
· Catalyst in the regioselective acylation of N-tosylhydrazide.
· Starting material in the synthesis of 4-aminopyridine derivatives for neurological disorder studies.
· Precursor for the synthesis of enantiomerically pure 4-(pyrrolidino)pyridine (PPY) derivatives by cyclocondensation reaction.

Specifications

Synonyms
AI3-52547 | Amaya | Avitrol | Dalfampridine (USAN) | Fampridine-PR | BH3B64OKL9 | DTXCID003870 | p-amino pyridine | BRN 0105782 | gamma-Aminopyridine | C5H6N2 | pyridin-4-amine | SMR000058211 | 4 Aminopyridine | 4- Aminopyridine | DALFAMPRIDINE [USP-RS] |
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Potassium channel blocker. Blocks Kv channels. Convulsant, and useful tool to model epileptiform activity in vitro .
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice, FedEx DG Service
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
BLOCKER
Mechanism of action
Voltage-gated potassium channel blocker
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Pubchem Sid504750504
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750504
Canonical SmilesC1=CN=CC=C1N
IUPAC Namepyridin-4-amine
InChIKeyNUKYPUAOHBNCPY-UHFFFAOYSA-N
INCHI1S/C5H6N2/c6-5-1-3-7-4-2-5/h1-4H,(H2,6,7)
Isomeric SMILES C1=CN=CC=C1N
WGK Germany 3
RTECS US1750000
UN Number 2671
Packing Group II
Molecular Weight 94.11
Beilstein 105782
Reaxy-Rn 105782
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105782&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
SuperclassOrganoheterocyclic compounds
ClassPyridines and derivatives
SubclassAminopyridines and derivatives
Intermediate Tree Nodes Not available
Direct ParentAminopyridines and derivatives
Alternative Parents Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Aminopyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring.
External Descriptors aromatic amine - aminopyridine
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CYP2D6 Tclin Cytochrome P450 2D6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA7 Tclin Potassium voltage-gated channel subfamily A member 7 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNC1 Tclin Potassium voltage-gated channel subfamily C member 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCND3 Tclin Potassium voltage-gated channel subfamily D member 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA10 Tclin Potassium voltage-gated channel subfamily A member 10 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA4 Tclin Potassium voltage-gated channel subfamily A member 4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA2 Tclin Potassium voltage-gated channel subfamily A member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNC2 Tclin Potassium voltage-gated channel subfamily C member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNC3 Tclin Potassium voltage-gated channel subfamily C member 3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNA5 Tclin Potassium voltage-gated channel subfamily A member 5 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNB1 Tclin Potassium voltage-gated channel subfamily B member 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNB2 Tclin Potassium voltage-gated channel subfamily B member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCND1 Tclin Potassium voltage-gated channel subfamily D member 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCND2 Tclin Potassium voltage-gated channel subfamily D member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
DHFR Tclin Dihydrofolate reductase (3072 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLG Tclin Plasminogen (2339 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
PRSS1 Tclin Trypsin I (2306 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 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
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
DRD1 Tclin Dopamine D1 receptor (9720 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
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
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
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 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
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA3 Tclin Voltage-gated potassium channel subunit Kv1.3 (1067 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNA1 Tclin Voltage-gated potassium channel subunit Kv1.1 (248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERG Tbio Transcriptional regulator ERG (5589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Cruzipain (33337 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
Slc5a7 Choline transporter (45 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
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTR1 Pteridine reductase 1 (345 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Scn2a Sodium channel alpha subunits; brain (Types I, II, III) (344 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.

32 results found

Lot NumberCertificate TypeDateItem
K2527290Certificate of AnalysisNov 14, 2025 A113920
K2527283Certificate of AnalysisNov 14, 2025 A113920
K2527282Certificate of AnalysisNov 14, 2025 A113920
K2527281Certificate of AnalysisNov 14, 2025 A113920
F2525085Certificate of AnalysisAug 01, 2024 A113920
I2404086Certificate of AnalysisAug 01, 2024 A113920
I2404085Certificate of AnalysisAug 01, 2024 A113920
E2516141Certificate of AnalysisApr 15, 2024 A113920
J2313044Certificate of AnalysisSep 14, 2023 A113920
J2313043Certificate of AnalysisSep 14, 2023 A113920
J2313042Certificate of AnalysisSep 14, 2023 A113920
I2517069Certificate of AnalysisSep 14, 2023 A113920
H2308461Certificate of AnalysisJul 20, 2023 A113920
H2308436Certificate of AnalysisJul 20, 2023 A113920
H2308434Certificate of AnalysisJul 20, 2023 A113920
H2308432Certificate of AnalysisJul 20, 2023 A113920
H2308433Certificate of AnalysisJul 20, 2023 A113920
E2325871Certificate of AnalysisMay 15, 2023 A113920
E2325862Certificate of AnalysisMay 15, 2023 A113920
E2325899Certificate of AnalysisMay 15, 2023 A113920
E2325890Certificate of AnalysisMay 15, 2023 A113920
E2325879Certificate of AnalysisMay 15, 2023 A113920
E2325875Certificate of AnalysisMay 15, 2023 A113920
E2325874Certificate of AnalysisMay 15, 2023 A113920
E2325872Certificate of AnalysisMay 15, 2023 A113920
E2325868Certificate of AnalysisMay 15, 2023 A113920
B2328408Certificate of AnalysisFeb 11, 2023 A113920
B2328407Certificate of AnalysisFeb 11, 2023 A113920
B2328399Certificate of AnalysisFeb 11, 2023 A113920
B2328398Certificate of AnalysisFeb 11, 2023 A113920
B2328397Certificate of AnalysisFeb 11, 2023 A113920
B2327040Certificate of AnalysisNov 11, 2021 A113920

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Chemical and Physical Properties
SolubilitySoluble in water(112 g/L at 20 deg C). Soluble in ethyl ether, benzene. Slightly soluble in ligroin. Very soluble in ethanol. Soluble in methanol, acetone, tetrahydrofuran, isopropanol, acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, and ethanol.
SensitivityMoisture sensitive,heat sensitive
Flash Point(°F)327°F
Flash Point(°C)156 °C
Boil Point(°C)287 ° C
Melt Point(°C)155-158 °C (lit.)
Molecular Weight94.110 g/mol
XLogP30.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass94.0531 Da
Monoisotopic Mass94.0531 Da
Topological Polar Surface Area38.900 Ų
Heavy Atom Count7
Formal Charge0
Complexity48.000
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. Chengxiang Feng, Jiacong Wu, Xinnan Ma, Juan Han, Lei Wang, Yun Wang.  (2023)  An efficient, recyclable and stable immobilized enzyme cascade catalytic system with visible-light driven for the removal of organic matter in water.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.148111]
2. Hongjing Wang, Lin Cui, Songliang Liu, Hongjie Yu, Kai Deng, You Xu, Xiaonian Li, Ziqiang Wang, Liang Wang.  (2023)  Ultrafine AuCu nanowires for electrocatalytic nitrogen fixation.  Inorganic Chemistry Frontiers,  11  (3): (892-898).  [PMID:] [10.1039/D3QI01771K]
3. Wenli Hou, Xianyu Kang, Jiajie Lin, Mengying Xie, Yancai Li.  (2023)  The preparation of AuNPs/B-dNACNs and their application in P-aminophenol electrochemical sensing.  NEW JOURNAL OF CHEMISTRY,  47  (45): (20838-20845).  [PMID:] [10.1039/D3NJ03366J]
4. Xinlei Zhang, Fei Wu, Guicun Li, Lei Wang, Jianfeng Huang, Aili Song, Alan Meng, Zhenjiang Li.  (2023)  Construction of intramolecular donor–acceptor type carbon nitride for photocatalytic hydrogen production.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:37951001] [10.1016/j.jcis.2023.10.152]
5. Yanqiu Zhang, Minrui Sun, Yang Lu, Mingguo Peng, Erdeng Du, Xia Xu.  (2023)  Nitrogen-Doped Carbon Dots Encapsulated a Polyoxomolybdate-Based Coordination Polymer as a Sensitive Platform for Trace Tetracycline Determination in Water.  Nanomaterials,  13  (19): (2676).  [PMID:37836317] [10.3390/nano13192676]
6. Jiuli Chang, Fengfeng Song, Fang Xu, Dapeng Wu, Yan Hou, Kai Jiang, Yuming Guo, Zhiyong Gao.  (2023)  Enhanced electrocatalytic efficiencies for water electrolysis and para-nitrophenol hydrogenation by self-supported nickel cobalt phosphide-nickel iron layered double hydroxide p-n junction.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:37783006] [10.1016/j.jcis.2023.09.156]
7. Yanqiu Zhang, Minrui Sun, Yang Lu, Xia Xu, Erdeng Du, Mingguo Peng.  (2023)  Simultaneous high-performance detection and removal of tetracycline with a polyoxomolybdate-based coordination polymer.  Progress in Natural Science-Materials International,      [PMID:] [10.1016/j.pnsc.2023.08.015]
8. Qian Qu, Huan Li, Shuman Li, Zhijie Hu, Mingzhao Zhu, Junhong Chen, Xuebiao Sun, Yuqi Tang, Zejun Zhang, Yuanzhu Mi, Weichu Yu.  (2023)  Synthesis and demulsification mechanism of an ionic liquid with four hydrophobic branches and four ionic centers.  CHEMOSPHERE,      [PMID:37598952] [10.1016/j.chemosphere.2023.139802]
9. Yang Cao, Yinhua Wan, Chulong Chen, Jianquan Luo.  (2023)  Catalyst-anchored secondary polymerization for highly permeable acid-resistant nanofiltration membrane preparation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2023.121991]
10. Fan Wenjun, Duan Zhiyao, Liu Wei, Mehmood Rashid, Qu Jiating, Cao Yucheng, Guo Xiangyang, Zhong Jun, Zhang Fuxiang.  (2023)  Rational design of heterogenized molecular phthalocyanine hybrid single-atom electrocatalyst towards two-electron oxygen reduction.  Nature Communications,  14  (1): (1-11).  [PMID:36918545] [10.1038/s41467-023-37066-y]
11. Huawei Fang, Jianyang Gao, Jing Wang, Jixiang Xu, Lei Wang.  (2023)  Oxygen-doped and pyridine-grafted g-C3N4 for visible-light driven peroxymonosulfate activation: Insights of enhanced tetracycline degradation mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.123565]
12. Jiacong Wu, Xinnan Ma, Ting He, Juan Han, Yan Zhu, Chunmei Li, Yun Wang.  (2023)  A photo-enzyme coupling catalysis system with high enzyme loading for the efficient degradation of BPA in water.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.123392]
13. Hongjing Wang, Shiqian Jiao, Songliang Liu, Kai Deng, Hongjie Yu, Xin Wang, You Xu, Ziqiang Wang, Liang Wang.  (2022)  Ultrafine PdAgAu alloy nanowires for ethanol oxidation electrocatalysis.  Journal of Materials Chemistry A,  10  (45): (24051-24055).  [PMID:] [10.1039/D2TA05672K]
14. Hai-Fang Mao, Hong-Qing Fu, Ji-Bo Liu, Yun Zhao.  (2022)  Cycloaddition of carbon dioxide and epoxides over Fe-PYPA: Synthetic optimization and mechanistic study.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2022.108629]
15. Chongfu Wu, Zhenhua Sun, Changshen Ye, Zhaoyang Qi, Jie Chen, Zhixian Huang, Ting Qiu.  (2022)  Encapsulation of HPW and preparation of composites rich in Zr-defects by manual grinding: Synergistic catalysis for efficient oxidative desulfurization at room temperature.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.138906]
16. Junxiu Ye, Gufeng Li, Yao Zhang, Shiju Ji, Min Yang, Lijun Luo, Hongbin Wang, Jiaxiong Li, Guizhen Li.  (2022)  Fabrication of organobentonite by microwave-assisted heating and its adsorption property for phenol.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,  98  (3): (583-590).  [PMID:] [10.1002/jctb.7154]
17. Wei-Dong Xiao, Ling-Ping Xiao, Wen-Zhe Xiao, Qiang Wang, Shang-Ru Zhai, Run-Cang Sun.  (2022)  The new identity of cellulose pulp: A green silver nanoparticles support for highly efficient catalytic hydrogenation of 4-nitrophenol.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2022.131833]
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