Allantoin - ≥98% , CAS No.97-59-6

CAS: 97-59-6 Cat. No.: A101660 Peso molecular: 158.12 Beilstein Registry Number: 102364 Número EC: 202-592-8
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
UNII-344S277G0Z | 5-Ureidohydantoin | 5-ureido-Hydantoin | EINECS 202-592-8 | MFCD00005260 | BL Vital | Scar Gel | Allantoin Cream | BL Vital Skin | Scar Care | Glyoxylic(acid) diureide | CCRIS 1958 | Kenaf wet wipe | Sol Mouthwash | (2,5-dioxoimidazolidi
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
A101660-25g
4
16,90US$
100g
A101660-100g
5
19,90US$
500g
A101660-500g
2
43,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature Ships Normal 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 23 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Synthesis of sulofenur analogs for use as antitumor agents.

Specifications

Sinónimos
UNII-344S277G0Z | 5-Ureidohydantoin | 5-ureido-Hydantoin | EINECS 202-592-8 | MFCD00005260 | BL Vital | Scar Gel | Allantoin Cream | BL Vital Skin | Scar Care | Glyoxylic(acid) diureide | CCRIS 1958 | Kenaf wet wipe | Sol Mouthwash | (2, 5-dioxoimidazolidi
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Purine metabolite via the uric acid pathway. Uric acid also reacts with free radicals to produce allantoin, thus allantoin may be a useful biomarker for oxidative stress.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504750363
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750363
Sonrisas canónicasC1(C(=O)NC(=O)N1)NC(=O)N
IUPAC Name(2,5-dioxoimidazolidin-4-yl)urea
InChIKeyPOJWUDADGALRAB-UHFFFAOYSA-N
INCHI1S/C4H6N4O3/c5-3(10)6-1-2(9)8-4(11)7-1/h1H,(H3,5,6,10)(H2,7,8,9,11)
Isómeros SMILES C1(C(=O)NC(=O)N1)NC(=O)N
WGK Alemania 1
RTECS YT1600000
Peso molecular 158.12
Beilstein 102364
Reaxy-Rn 83514
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=83514&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
ClaseAzoles
SubclassImidazoles
Intermediate Tree Nodes Not available
Direct ParentImidazoles
Alternative Parents Isoureas  Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Imines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Imidazole - Isourea - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Carboximidic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Imine - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as imidazoles. These are compounds containing an imidazole ring, which is an aromatic five-member ring with two nitrogen atoms at positions 1 and 3, and three carbon atoms.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A498 (42825 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXF 393 (41971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TK-10 (45540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI/ADR-RES (33767 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T47D (39041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EKVX (44102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCC 2998 (41480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-92 (41141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs-578T (29457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGROV-1 (47897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LOX IMVI (44321 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-62 (47048 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-435 (38290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-N (28205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 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
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
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
C6 (2371 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:

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

38 results found

Lot NumberCertificate TypeFechaArticulo
J2209034Certificate of AnalysisApr 02, 2026 A101660
D2602196Certificate of AnalysisMar 21, 2026 A101660
D2602168Certificate of AnalysisMar 21, 2026 A101660
D2602169Certificate of AnalysisMar 21, 2026 A101660
D2602170Certificate of AnalysisMar 21, 2026 A101660
D2602171Certificate of AnalysisMar 21, 2026 A101660
E2423141Certificate of AnalysisFeb 05, 2026 A101660
K2307083Certificate of AnalysisAug 11, 2025 A101660
I2509235Certificate of AnalysisJul 22, 2025 A101660
I2509219Certificate of AnalysisJul 22, 2025 A101660
H2511213Certificate of AnalysisJul 22, 2025 A101660
H2511212Certificate of AnalysisJul 22, 2025 A101660
H2511211Certificate of AnalysisJul 22, 2025 A101660
E2325062Certificate of AnalysisFeb 07, 2025 A101660
K2408185Certificate of AnalysisOct 28, 2024 A101660
K2408183Certificate of AnalysisOct 28, 2024 A101660
K2408184Certificate of AnalysisOct 28, 2024 A101660
J2209056Certificate of AnalysisJul 19, 2024 A101660
E2423432Certificate of AnalysisMay 10, 2024 A101660
E2423140Certificate of AnalysisMay 10, 2024 A101660
E2423139Certificate of AnalysisMay 10, 2024 A101660
C2429002Certificate of AnalysisMar 13, 2024 A101660
C2429003Certificate of AnalysisMar 13, 2024 A101660
L2327032Certificate of AnalysisOct 25, 2023 A101660
K2307084Certificate of AnalysisOct 25, 2023 A101660
K2307027Certificate of AnalysisOct 25, 2023 A101660
I2113164Certificate of AnalysisJun 13, 2023 A101660
I2111098Certificate of AnalysisJun 12, 2023 A101660
I2111108Certificate of AnalysisJun 12, 2023 A101660
I2111084Certificate of AnalysisJun 12, 2023 A101660
H2109022Certificate of AnalysisMay 10, 2023 A101660
L2003096Certificate of AnalysisSep 16, 2022 A101660
L2003095Certificate of AnalysisSep 16, 2022 A101660
J2209033Certificate of AnalysisAug 26, 2022 A101660
J2209040Certificate of AnalysisAug 26, 2022 A101660
D2326037Certificate of AnalysisAug 26, 2022 A101660
E2310658Certificate of AnalysisJun 05, 2021 A101660
E2310652Certificate of AnalysisJun 05, 2021 A101660

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Propiedades químicas y físicas
SolubilidadSlightly soluble in water. Freely soluble in alkalis
SensibilidadMoisture sensitive.
Punto de fusión (°C)238-240°C
Peso molecular158.120 g/mol
XLogP3-2.200
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass158.044 Da
Monoisotopic Mass158.044 Da
Topological Polar Surface Area113.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity225.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
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. Qiuzheng Du, Wenjun Guo, Yingying Shi, Ziwei Jing, Zhi Sun.  (2023)  Boric acid-functionalized lanthanide metal-organic framework used as a ratiometric fluorescence probe for uric acid detection.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2023.109161]
2. Fanxing Xu, Jingxian Wu, Yumei Hu, Chun Chu, Wenjun Liu, Xiang Li, Wen Zheng, Weishuo Yang, Boyan Zhao, Jiangxue Guo, Zhenzhong Wang, Ying Jia, Wei Xiao.  (2023)  Mechanisms of action underlying the effect of Tongsaimai on wound healing based on experimental and network pharmacology.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:37031824] [10.1016/j.jep.2023.116451]
3. Xu Zhang, Xiaotong Wang, Rui Shi, Xiaoku Ran, Xiahong He, Deqiang Dou.  (2023)  Effective substances and mechanism of red ginseng on rats with spleen-deficiency syndrome based on the substance and energy metabolism as well as the “brain-gut” axis.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:37003398] [10.1016/j.jep.2023.116438]
4. Gang Wang, Jiali Li, Jing Ji, Lishuang Zhang, Bowen Li, Jiaqi Zhang, Xinya Wang, Wenju Song, Chunfeng Guan.  (2023)  Combined application of allantoin and strain JIT1 synergistically or additively promotes the growth of rice under 2, 4-DCP stress by enhancing the phosphate solubility, improving soil enzyme activities and photosynthesis.  JOURNAL OF PLANT PHYSIOLOGY,      [PMID:36739690] [10.1016/j.jplph.2023.153941]
5. Qiqin Wang, Lingjue Sun, Huihui Wu, Ning Deng, Xianglong Zhao, Jingwei Zhou, Tingting Zhang, Hai Han, Zhengjin Jiang.  (2022)  Rapid fabrication of zwitterionic sulfobetaine vinylimidazole-based monoliths via photoinitiated copolymerization for hydrophilic interaction chromatography.  Journal of Pharmaceutical Analysis,      [PMID:36320596] [10.1016/j.jpha.2022.05.008]
6. Haojiang Xie, Qiao Bai, Fankai Kong, Yang Li, Xiaoying Zha, Lingqin Zhang, Yiming Zhao, Shasha Gao, Ping Li, Qifeng Jiang.  (2022)  Allantoin-functionalized silk fibroin/sodium alginate transparent scaffold for cutaneous wound healing.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:35358577] [10.1016/j.ijbiomac.2022.03.147]
7. Lingjue Sun, Dongsheng Xu, Yuan Shen, Jacques Crommen, Qiqin Wang, Zhengjin Jiang.  (2021)  Photo-assisted generation of versatile zwitterionic carboxybetaine-based hypercrosslinked polymers for separation science.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2021.133374]
8. Liu Donghao, Yang Ping, Wang Fangqi, Wang Cong, Chen Li, Ye Sijing, Dramou Pierre, Chen Jianhua, He Hua.  (2021)  Study on performance of mimic uricase and its application in enzyme-free analysis.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  413  (26): (6571-6580).  [PMID:34417645] [10.1007/s00216-021-03620-0]
9. Ling Zhou, Kan Hu, Tengguo Dong, Qian Wang, Hengming Huang, Chunhua Lu, Jiahui Kou, Zhongzi Xu.  (2021)  Carbon ring and molecular scaffold co-doped g-C3N4 heterostructural nanosheets for highly efficient hydrogen evolution.  MATERIALS RESEARCH BULLETIN,      [PMID:] [10.1016/j.materresbull.2021.111482]
10. Zhou Ling, Sun Menglong, Kou Jiahui, Lu Chunhua, Li Ling, Zhang Fangshu, Xu Zhongzi.  (2020)  Embedding of stereo molecular scaffold into the planar g-C3N4 nanosheets for efficient photocatalytic hydrogen evolution under ordinary pressure.  JOURNAL OF MATERIALS SCIENCE,  56  (2): (1630-1642).  [PMID:] [10.1007/s10853-020-05287-x]
11. Xueying Liu, Xiaoku Ran, Muhammad Riaz, Haixue Kuang, Deqiang Dou, Decheng Cai.  (2019)  Mechanism Investigation of Tagetes patula L. against Chronic Nonbacterial Prostatitis by Metabolomics and Network Pharmacology.  MOLECULES,  24  (12): (2266).  [PMID:31216740] [10.3390/molecules24122266]
12. Nan Zhang, Tisong Liang, Quan Jin, Cai Shen, Yifan Zhang, Pu Jing.  (2019)  Chinese yam (Dioscorea opposita Thunb.) alleviates antibiotic-associated diarrhea, modifies intestinal microbiota, and increases the level of short-chain fatty acids in mice.  FOOD RESEARCH INTERNATIONAL,      [PMID:31229072] [10.1016/j.foodres.2019.04.016]
13. Chen Si, Wang Yating, An Zhihang, Ma Meng, Shi Yanqin, Wang Xu.  (2018)  Stability, antibacterial ability, and inhibition of “zinc burning” of amitrole as thermal stabilizer for transparent poly(vinyl chloride).  JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY,  137  (2): (437-446).  [PMID:] [10.1007/s10973-018-7929-9]
14. Zhong Shengliang, Li Bingmei, Ji Yanhua, Zeng Chenghui.  (2016)  Multifunctional Coordination Polymer Nanoparticles Based on Allantoin: Single Peak Upconversion Emission, Drug Delivery and Cytotoxicity Study.  Journal of Inorganic and Organometallic Polymers and Materials,  26  (3): (527-535).  [PMID:] [10.1007/s10904-016-0360-4]
15. Xu Xiaopeng, Chen Si, Wu Bozhen, Ma Meng, Shi Yanqin, Wang Xu.  (2014)  Effect of allantoin on the stabilization efficiency of Ca–Zn thermal stabilizers for poly(vinyl chloride).  JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY,  119  (1): (597-603).  [PMID:] [10.1007/s10973-014-4168-6]
16. Manjila Adhikari, Bianza Moise Bakadia, Li Wang, Ying Li, Zhijun Shi, Guang Yang.  (2024)  Electricallymodified bacterial cellulose tailored with plant based green materials for infected wound healing applications.  Biomaterials Advances,      [PMID:39481142] [10.1016/j.bioadv.2024.214087]
17. Yizhan Wang, Yunhui Shi, Jiawei Qiu, JiaBao Cheng, Yao Xu, Yongxin Wang.  (2024)  Insights into molecular interactions at organic-MBene heterointerfaces for efficient Zn-ion storage.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:39241451] [10.1016/j.jcis.2024.08.247]
18. Yue Kong, Xu Fan, Rongkai Wu, Shibin Nie, Chao Liu, Xiaoyong Liu, Guangyi Zhang, Bihe Yuan.  (2024)  Multifunctional flame-retardant cotton fabric with hydrophobicity and electrical conductivity for wearable smart textile and self-powered fire-alarm system.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.150677]
19. Liang Lai, Mengyao Zhang, Tong Li, Jiahuan Qu, Dongsheng Xu, Pei Yu, Zhengjin Jiang.  (2024)  Preparation and evaluation of a piperidinium-sulfonate based zwitterionic monolith for HILIC separation.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:38598890] [10.1016/j.chroma.2024.464864]
20. Qiaoxuan Zhang, Ning Deng, Yingying Dai, Min Zhan, Huihui Wu, Jialin Zeng, Qiqin Wang, Zhengjin Jiang.  (2024)  Zwitterionic sulfobetaine-based hypercrosslinked hydrophilic materials for bioanalysis.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.153018]
21. Qingquan Guo, Yudong Zhang, Chuanjin Tang, Qiuru Li, Fei Liu, Zhenming He, Chenyang Jiang, Jun Xu, Haishan Zhao.  (2025)  4-Hydroxyacetophenone is an Antipigmentation Reagent via Inhibiting Tryrosinase Activity.  ACS Omega,      [PMID:40821508] [10.1021/acsomega.5c03812]
22. Chen Guo, Yixiang Sun, Hongjun Chen, Guangyao Yin, Yizhi Song.  (2025)  Identification and assessment of Pichia kudriavzevii YS711 isolated from “Jiangshui” with the capacity for uric acid metabolism.  MICROBIOLOGICAL RESEARCH,      [PMID:40347632] [10.1016/j.micres.2025.128200]
23. Minyi Yuan, Zheng Zhao, Ji Wu, Sumin Bian, Yuling Liao, Ying Zhou, Huikai Shao, Zhengjin Jiang, Qiqin Wang.  (2025)  Zwitterionic Imidazolium Sulfonate Functionalized Polymeric Monolith for Mixed-Mode HILIC/RPLC Applications.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:41106254] [10.1016/j.chroma.2025.466462]
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