4,4'-Diaminodiphenyl Sulfone(DDS) - Moligand™, 10mM in DMSO , CAS No.80-08-0

CAS: 80-08-0 Cat. No.: D426062 Peso molecular: 248.3 Beilstein Registry Number: 788055 Número EC: 201-248-4
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
dapsone|80-08-0|4,4'-Sulfonyldianiline|4,4'-Diaminodiphenyl sulfone|Diaphenylsulfone|4,4'-Diaminodiphenylsulfone|Dapson|4-Aminophenyl sulfone|Novophone|DADPS|Diaphenylsulfon|Dapsonum|Diphenasone|Sulphadione|Aczone|Sulfona|Bis(4-aminophenyl) sulfone|p-Amin
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
D426062-1ml
2
26,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, 10mM in DMSO Moligand™ 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 114 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
dapsone | 80-08-0 | 4, 4'-Sulfonyldianiline | 4, 4'-Diaminodiphenyl sulfone | Diaphenylsulfone | 4, 4'-Diaminodiphenylsulfone | Dapson | 4-Aminophenyl sulfone | Novophone | DADPS | Diaphenylsulfon | Dapsonum | Diphenasone | Sulphadione | Aczone | Sulfona | Bis(4-aminophenyl) sulfone | p-Amin
Especificaciones y pureza
Moligand™, 10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Antibacterial and anti-inflammatory agent. Neuroprotective and anti-apoptotic effects.
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.
Grado
Moligand™
Tipo de acción
INHIBITOR
Propiedades del producto
ALogP1
Nombres e identificadores
Sonrisas canónicasC1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N
IUPAC Name4-(4-aminophenyl)sulfonylaniline
InChIKeyMQJKPEGWNLWLTK-UHFFFAOYSA-N
INCHI1S/C12H12N2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H,13-14H2
Isómeros SMILES C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N
WGK Alemania 1
RTECS BY8925000
Peso molecular 248.3
Beilstein 788055
Reaxy-Rn 788055
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=788055&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
SubclassBenzenesulfonyl compounds
Intermediate Tree Nodes Not available
Direct ParentBenzenesulfonyl compounds
Alternative Parents Aniline and substituted anilines  Sulfones  Primary amines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzenesulfonyl group - Aniline or substituted anilines - Sulfonyl - Sulfone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzenesulfonyl compounds. These are aromatic compounds containing a benzenesulfonyl group, which consists of a monocyclic benzene moiety that carries a sulfonyl group.
External Descriptors sulfone - substituted aniline
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
MPO Tchem Myeloperoxidase (1 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
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
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
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
MAOB Tclin Monoamine oxidase B (8835 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
Objetivos asociados (no humanos)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
folP Dihydropteroate synthase (129 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
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecium (13803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium avium (4587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lacticaseibacillus casei (578 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 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
Candida tropicalis (8381 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania donovani (89745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium berghei (192651 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
Trypanosoma brucei rhodesiense (7991 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium vivax (152 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPPK-DHPS Dihydropteroate synthetase, putative (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium leprae (477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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
SensibilidadMoisture sensitive.
Punto de fusión (°C)173-178°C
Peso molecular248.300 g/mol
XLogP31.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass248.062 Da
Monoisotopic Mass248.062 Da
Topological Polar Surface Area94.600 Ų
Heavy Atom Count17
Formal Charge0
Complexity306.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Fan Shu, Weilin Chen, Gang Liu.  (2023)  Functionalization of Violet Phosphorus Quantum Dots with Azo-Containing Star-Shape Polymer for Optically Controllable Memory.  Processes,  11  (12): (3429).  [PMID:] [10.3390/pr11123429]
2. Congcong Zhai, Wenchao Zhang, Rongjie Yang.  (2023)  Synthesis of a novel bis(diphenylphosphinyl)-containing pyromellitimide and its application in epoxy resins.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2023.110574]
3. Chunying Min, Zhaolong Sun, Qiuying Li, Hang Yu, Zhiwei Xu, Hongyu Liang.  (2023)  Three-dimensional interconnected graphene architecture reinforced epoxy composite with superior mechanical and tribological properties.  Journal of Materials Research and Technology-JMR&T,      [PMID:] [10.1016/j.jmrt.2023.10.099]
4. Qing Wu, Bolin Xiao, Qianli Liu, Hao Deng, Ziyi Ye, Yating Li, Renjie Yao, Jianfeng Zhu.  (2023)  New strategy for enhancing interfacial adhesion between carbon fiber and epoxy by using mussel-inspired polydopamine-Fe complex nanospheres.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2023.111032]
5. Xian Hou, Zhenjia Yuan, Jinlong Liu, Hongzhen Ma.  (2023)  Multifunctional Dapsone Additives Prepare Efficient and Stable Perovskite Solar Cells.  ACS Applied Energy Materials,      [PMID:] [10.1021/acsaem.3c01209]
6. Zichun Ding, Lishuai Zong, Chenghao Wang, Siying Wang, RunZe Liu, Xigao Jian, Jinyan Wang.  (2023)  A new approach to enhance the performance of phthalonitrile: study of carborane curing agents with dual functions.  Molecular Systems Design & Engineering,  (12): (1492-1497).  [PMID:] [10.1039/D3ME00103B]
7. Changhai Zhang, Zeyang Liu, Tiandong Zhang, Xubin Wang, Chao Yin, Xianli Liu, Qingguo Chi.  (2023)  High-temperature resistance and excellent electrical insulation in epoxy resin blends.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (35): (e54359).  [PMID:] [10.1002/app.54359]
8. Hongwei Gu, Qi Cao, Jiahui Li, Jing Zhao, Shouhai Zhang, Xigao Jian, Zhihuan Weng.  (2023)  Enhancing the comprehensive performance of bisphenol A epoxy resin via blending with a bio-based counterpart.  POLYMER,      [PMID:] [10.1016/j.polymer.2023.126038]
9. Zhengyan Chen, Maoyu Zhang, Penggang Ren, Zhou Lan, Zhengzheng Guo, Hongxia Yan, Yanling Jin, Fang Ren.  (2023)  Enhanced mechanical and tribological properties of epoxy composites reinforced by novel hyperbranched polysiloxane functionalized graphene/MXene hybrid.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.143086]
10. Yongzheng Zhao, Yan Li, Jiaxuan Li, Yifan Xiao, Wenmin Mu, Zhongwei Wang, Liang Song, Jinhong Yu.  (2023)  Flame Retardancy of Epoxy Resins Modified with Few-Layer Black Phosphorus.  Polymers,  15  (7): (1655).  [PMID:37050271] [10.3390/polym15071655]
11. Xinxin Fang, Xin Guo, Weilin Tang, Qun Gu, Yue Wu, Hua Sun, Junfei Gao.  (2023)  Efficient Toughening of DGEBA with a Bio-Based Protocatechuic Acid Derivative.  ACS Omega,      [PMID:36969454] [10.1021/acsomega.2c07140]
12. Lifen Tong, Ting Wang, Yaqi Chen, Guo Lin, Liang He, Xiaobo Liu.  (2023)  Nitrogen self-doped porous lamellar carbon with superior electrochemical performance.  DIAMOND AND RELATED MATERIALS,      [PMID:] [10.1016/j.diamond.2023.109787]
13. Xiao-Lu Pu, Song Gu, Yan-Fang Xiao, Yu-Zhong Wang, Li Chen.  (2022)  Novel organophosphonate-decorated WS2 nanosheets towards flame retardancy and mechanical enhancement of epoxy resin.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2022.110170]
14. Shao-Dong Xu, Song Gu, Xiao-Lu Pu, Yan-Fang Xiao, Jia-Hui Lu, Yu-Zhong Wang, Li Chen.  (2022)  Reaction-induced phase separation towards in situ network in epoxy resins for simultaneously improving thermal conductivity and fire safety.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2022.110326]
15. Shao-Dong Xu, Song Gu, Xiao-Lu Pu, Yan-Fang Xiao, Jia-Hui Lu, Yu-Zhong Wang, Li Chen.  (2022)  In situ phase separation of novel phosphorus-containing polyester in epoxy resins towards simultaneously improved thermal conductivity and fire safety.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2022.110113]
16. Chi Qingguo, Zhang Xiaowen, Zhang Changhai, Feng Yu, Tang Chao, Li Zhonghua, Zhang Tiandong.  (2022)  Heat-resistant and electrical properties of bismaleimide modified epoxy resin.  JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS,  33  (22): (17868-17876).  [PMID:] [10.1007/s10854-022-08650-7]
17. Rui Cai, Jinlong Zhao, Naixin Lv, Anqing Fu, Chengxian Yin, Chengjun Song, Min Chao.  (2022)  Curing and Molecular Dynamics Simulation of MXene/Phenolic Epoxy Composites with Different Amine Curing Agent Systems.  Nanomaterials,  12  (13): (2249).  [PMID:35808085] [10.3390/nano12132249]
18. Tingting Wang, Li Yuan, Guozheng Liang, Aijuan Gu.  (2022)  Constructing nano SiO2-anchored hyperbranched polymer hybrid architectures for thermosetting epoxy systems with outstanding mechanical property.  POLYMER COMPOSITES,  43  (8): (5375-5389).  [PMID:] [10.1002/pc.26841]
19. Yunxia Yang, Dan Xiao.  (2022)  Fabrication of two multifunctional phosphorus–nitrogen flame retardants toward improving the fire safety of epoxy resin.  E-POLYMERS,  22  (1): (430-444).  [PMID:] [10.1515/epoly-2022-0042]
20. Shaoling Lin, Boqing Tao, Xiaomin Zhao, Guohua Chen, De-Yi Wang.  (2021)  Surface Functionalization of Black Phosphorus via Amine Compounds and Its Impacts on the Flame Retardancy and Thermal Decomposition Behaviors of Epoxy Resin.  Polymers,  13  (21): (3635).  [PMID:34771191] [10.3390/polym13213635]
21. Hongmei Chen, Yanyun Fan, Zheng Fan, Hongyan Xu, Danfeng Cui, Chenyang Xue, Wendong Zhang.  (2021)  Electronic tuning of g-C3N4 via competitive coordination to stimulate high-efficiently photocatalytic for hydrogen evolution.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2021.162027]
22. Tian-Yu Gao, Fen-Dou Wang, Yu Xu, Chun-Xiang Wei, San-E Zhu, Wei Yang, Hong-Dian Lu.  (2021)  Luteolin-based epoxy resin with exceptional heat resistance, mechanical and flame retardant properties.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.131173]
23. Long Ni, Yinfu Luo, Xionghou Peng, Shengtai Zhou, Huawei Zou, Mei Liang.  (2021)  Investigation of the properties and structure of semi-rigid closed-cellular polyimide foams with different diamine structures.  POLYMER,      [PMID:] [10.1016/j.polymer.2021.123957]
24. Kaiyi Tian, Senyuan Yang, Jiaxuan Niu, Hanxiang Wang.  (2021)  Enhanced Thermal Conductivity and Mechanical Toughness of the Epoxy Resin by Incorporation of Mesogens Without Nanofillers.  IEEE Access,      [PMID:] [10.1109/ACCESS.2021.3058612]
25. Yuan Zu, Lishuai Zong, Jinyan Wang, Xigao Jian.  (2021)  Kinetic analysis of the curing of branched phthalonitrile resin based on dynamic differential scanning calorimetry.  POLYMER TESTING,      [PMID:] [10.1016/j.polymertesting.2021.107062]
26. Jiandong Zuo, Zhao Liu, Chaoyun Luo, Feng Lin.  (2020)  Preparation and properties of high refractive index polythioetherimide film based on thiol-ene click chemistry.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2020.106048]
27. Yuan Zu, Fengfeng Zhang, Dandan Chen, Lishuai Zong, Jinyan Wang, Xigao Jian.  (2020)  Wave-transparent composites based on phthalonitrile resins with commendable thermal properties and dielectric performance.  POLYMER,      [PMID:] [10.1016/j.polymer.2020.122490]
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