p-Hydroxybenzoic acid - ≥99% , CAS No.99-96-7

CAS: 99-96-7 Cat. No.: H108508 Molecular Weight: 138.12 Beilstein Registry Number: 970950 EC Number: 202-804-9
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
4-HYDROXYBENZOIC ACID [INCI] | BIDD:ER0706 | Benzoic acid, p-hydroxy | p-Oxybenzoesaure [German] | SALICYLIC ACID IMPURITY A (EP IMPURITY) | 4-HYDROXYBENZOIC ACID [FHFI] | 4-Hydroxybenzoic acid, ReagentPlus(R), 99% | 4-Carboxyphenol | 4-HBA | 4-HYDROXYBEN
Storage
Protected from light,Room temperature
Shipped In
Normal
Size
Status
Price
Qty
25g
H108508-25g
1
$9.90
100g
H108508-100g
2
$12.90
500g
H108508-500g
3

$28.90

$43.90
Save $15.00 (34.17%)
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,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 315 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
4-HYDROXYBENZOIC ACID [INCI] | BIDD:ER0706 | Benzoic acid, p-hydroxy | p-Oxybenzoesaure [German] | SALICYLIC ACID IMPURITY A (EP IMPURITY) | 4-HYDROXYBENZOIC ACID [FHFI] | 4-Hydroxybenzoic acid, ReagentPlus(R), 99% | 4-Carboxyphenol | 4-HBA | 4-HYDROXYBEN
Specifications & Purity
≥99%
Storage
Protected from light, Room temperature
Shipped In
Normal
Purity
≥99%
Names and Identifiers
Pubchem Sid508813306
Canonical SmilesC1=CC(=CC=C1C(=O)O)O
IUPAC Name4-hydroxybenzoic acid
InChIKeyFJKROLUGYXJWQN-UHFFFAOYSA-N
INCHI1S/C7H6O3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H,(H,9,10)
Isomeric SMILES C1=CC(=CC=C1C(=O)O)O
WGK Germany 1
RTECS DH1925000
Molecular Weight 138.12
Beilstein 970950
Reaxy-Rn 970950
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=970950&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.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentHydroxybenzoic acid derivatives
Alternative Parents Benzoic acids  Benzoyl derivatives  1-hydroxy-2-unsubstituted benzenoids  Monocarboxylic acids and derivatives  Carboxylic acids  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Hydroxybenzoic acid - Benzoic acid - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. These are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.
External Descriptors monohydroxybenzoic acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABAT Tclin Gamma-amino-N-butyrate transaminase (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARA Tclin Peroxisome proliferator-activated receptor alpha (9197 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH5A1 Tclin Succinate semialdehyde dehydrogenase (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NEU3 Tchem Sialidase 3 (398 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TPMT Tchem Thiopurine S-methyltransferase (45 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-1080 (3966 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LoVo (4724 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
N9 (414 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PANC-1 (6144 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HUVEC (11049 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KB (17409 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TLR2 Tchem Toll-like receptor 2 (975 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (300 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC22A8 Tclin Solute carrier family 22 member 8 (241 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 (221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A7 Tbio UDP-glucuronosyltransferase 1-7 (106 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A8 Tbio UDP-glucuronosyltransferase 1-8 (233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 (343 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UGT1A10 Tbio UDP-glucuronosyltransferase 1-10 (257 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ralstonia solanacearum (520 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Agrobacterium tumefaciens (620 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus flavus (8875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sorghum halepense (127 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Penicillium chrysogenum (1593 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meloidogyne incognita (862 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
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BV-2 (3710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-22 (3261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ambrosia artemisiifolia (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Chenopodium album (769 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Convolvulaceae (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cornus florida (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Curtobacterium flaccumfaciens (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Datura stramonium (35 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Helicoverpa zea (137 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Malassezia furfur (70 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nasturtium officinale (18 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pectobacterium carotovorum (295 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Senna obtusifolia (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sida spinosa (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sorghum (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Heterodera zeae (651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Colletotrichum acutatum (300 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hylobius abietis (106 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.

35 results found

Lot NumberCertificate TypeDateItem
E2626445Certificate of AnalysisMay 11, 2026 H108508
E2626444Certificate of AnalysisMay 11, 2026 H108508
E2626443Certificate of AnalysisMay 11, 2026 H108508
E2621776Certificate of AnalysisMay 11, 2026 H108508
E2626446Certificate of AnalysisMay 11, 2026 H108508
E2621404Certificate of AnalysisMay 11, 2026 H108508
E2621407Certificate of AnalysisMay 11, 2026 H108508
E2621416Certificate of AnalysisMay 11, 2026 H108508
K2520006Certificate of AnalysisAug 16, 2025 H108508
I2501486Certificate of AnalysisAug 16, 2025 H108508
I2501485Certificate of AnalysisAug 16, 2025 H108508
I2501333Certificate of AnalysisAug 16, 2025 H108508
G2524021Certificate of AnalysisDec 13, 2024 H108508
L2426461Certificate of AnalysisDec 13, 2024 H108508
L2426449Certificate of AnalysisDec 13, 2024 H108508
L2426450Certificate of AnalysisDec 13, 2024 H108508
L2426456Certificate of AnalysisDec 13, 2024 H108508
K2415393Certificate of AnalysisNov 02, 2024 H108508
K2415392Certificate of AnalysisNov 02, 2024 H108508
E2506173Certificate of AnalysisJul 23, 2024 H108508
J2428651Certificate of AnalysisJul 18, 2024 H108508
E2506179Certificate of AnalysisJul 18, 2024 H108508
E2506174Certificate of AnalysisJul 10, 2024 H108508
J2428646Certificate of AnalysisJul 10, 2024 H108508
B2324569Certificate of AnalysisNov 25, 2022 H108508
B2324570Certificate of AnalysisNov 25, 2022 H108508
G2430141Certificate of AnalysisNov 25, 2022 H108508
C2408015Certificate of AnalysisJul 16, 2022 H108508
I2222834Certificate of AnalysisJul 16, 2022 H108508
I2222833Certificate of AnalysisJul 16, 2022 H108508
I2222832Certificate of AnalysisJul 16, 2022 H108508
C2205286Certificate of AnalysisDec 24, 2021 H108508
C2205275Certificate of AnalysisDec 24, 2021 H108508
C2205261Certificate of AnalysisDec 24, 2021 H108508
D2126224Certificate of AnalysisMay 07, 2021 H108508

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Chemical and Physical Properties
SolubilityEasily soluble in ethanol, soluble in ether and acetone, slightly soluble in water and chloroform, almost insoluble in carbon disulfide.
SensitivityLight sensitive.
Flash Point(°C)199℃
Melt Point(°C)214-217°C
Molecular Weight138.120 g/mol
XLogP31.600
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass138.032 Da
Monoisotopic Mass138.032 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count10
Formal Charge0
Complexity125.000
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. Haining Du, Jiaxin Li, Xiangjuan Wei, Daqian Yang, Boya Zhang, Xingpei Fan, Meimei Zhao, Ruijiao Zhu, Ziyi Zhang, Yuxia Zhang, Xiaoyan Li, Ning Gu.  (2024)  Methylparaben induces hepatic glycolipid metabolism disorder by activating the IRE1α-XBP1 signaling pathway in male mice.  ENVIRONMENT INTERNATIONAL,      [PMID:38262168] [10.1016/j.envint.2024.108445]
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8. Daihong Gao, Denghao Ouyang, Xuebing Zhao.  (2023)  Controllable oxidative depolymerization of lignin to produce aromatic aldehydes and generate electricity under mild conditions with direct biomass fuel cells as flexible reactors.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.147874]
9. Jinxin Li, Hao Zhang, Ling Zhu, Gangcheng Wu, Hui Zhang.  (2023)  Influence of in vitro gastrointestinal digestion and colonic fermentation on carbonyl scavenging capacity of fiber-bound polyphenols from quinoa.  Food & Function,  14  (23): (10581-10590).  [PMID:37955444] [10.1039/D3FO03000H]
10. Yueqin Li, Yunzhen Zhang, Lezhen Dong, Ying Li, Yahui Liu, Yang Liu, Lingyi Liu, Lianliang Liu.  (2023)  Fermentation of Lactobacillus fermentum NB02 with feruloyl esterase production increases the phenolic compounds content and antioxidant properties of oat bran.  FOOD CHEMISTRY,      [PMID:37897817] [10.1016/j.foodchem.2023.137834]
11. Faguang Ma, Ming Yan, Rongxin Lin, Yilin Wu, Jianming Pan.  (2023)  Boronate-affinity sol–gel-imprinted membranes with MOFs-functionalized rotary-evaporating layers for high-precision specific recognition.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125458]
12. Liu Xinru, Ma Qianwei, Sun Yongjun, Ju Wenming, Kumrungsee Thanutchaporn, Zhou Zhongkai, Wang Lijuan, Cao Ruge.  (2023)  Effects of Processings and Complexation on Solubility, Antioxidant and Antibacterial Properties of Buckwheat Polyphenols.  Food and Bioprocess Technology,      [PMID:] [10.1007/s11947-023-03217-8]
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15. Xinlu Liu, Xiaoqian Chen, Huiyang Bian, Shuzhen Ni, Zongquan Li, Na Liu, Menghua Qin, Fengshan Zhang.  (2023)  Highly hydrophobic cotton fabric by in-situ co-deposition of lignin/metal particles for oil/water separation.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2023.117393]
16. Tianyuan Xu, Ting Chen, Zhenhua Chen, Yijun Cao, Yaowen Xing, Xiahui Gui.  (2023)  Oxalate enhanced aniline degradation by goethite: Structural dependent activity, hydroxyl radicals generation and toxicity evaluation.  CHEMOSPHERE,      [PMID:37572712] [10.1016/j.chemosphere.2023.139790]
17. Fangxin Deng, Qingze Chen, Yanping Zhu, Xiaoliang Liang, Runliang Zhu, Yunfei Xi.  (2023)  Hydrothermally treated peat/magnetite composites as highly efficient heterogeneous Fenton catalyst: Integrating multiple reaction mechanisms to enhance the catalytic reactivity for BPA removal.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.144946]
18. Xiaohui Fan, Jinjin Zhao, Cheng Cheng, Yin Xu, Hui Zhang.  (2023)  Engineered Fe-doped activated carbon from industry waste for peroxymonosulfate activation: Performance and mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.124607]
19. Jiangping Cao, Yifei He, Xiaoshuo Zhang, Lei Shi, Baizhao Zeng, Faqiong Zhao.  (2023)  Development of a tributyl phosphate-based hydrophobic deep eutectic solvent for liquid-liquid microextraction of total parabens in beverages.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2023.122593]
20. Xin Lv, Chenying Zhou, Zhichao Shen, Yuchen Zhang, Chuanshu He, Ye Du, Zhaokun Xiong, Rongfu Huang, Peng Zhou, Bo Lai.  (2023)  Waste leather derived porous carbon boosted Fenton oxidation towards removal of diethyl phthalate: Mechanism and long-lasting performance.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:37451102] [10.1016/j.jhazmat.2023.132040]
21. Dong Li, Chunran Zhou, Shuai Wang, Zhan Hu, Jia Xie, Canping Pan, Ranfeng Sun.  (2023)  Imidacloprid-induced stress affects the growth of pepper plants by disrupting rhizosphere-plant microbial and metabolite composition.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:37437628] [10.1016/j.scitotenv.2023.165395]
22. Zhenyu Li, Enhui Du, Panpan Hao, Liyuan Huai, Yang Zhong, Soliman I. El-Hout, Chunlin Chen, Jian Zhang.  (2023)  Diluted oxygen realizes high productivity of 2,5-Furandicarboxylic acid under ambient temperature.  CATALYSIS TODAY,      [PMID:] [10.1016/j.cattod.2023.114277]
23. Longwei Shi, Zheng Zhao, Lishuai Zong, Jinyan Wang, Xigao Jian.  (2023)  Reducing the dielectric loss of poly(aryl ether)s by grafting.  POLYMERS FOR ADVANCED TECHNOLOGIES,  34  (10): (3125-3136).  [PMID:] [10.1002/pat.6127]
24. Shuai Zhang, Mei Deng, Ruifen Zhang, Xuchao Jia, Fei Huang, Dong Zhao, Lihong Dong, Jianwei Chi, Zhida Sun, Qin Ma, Mingwei Zhang.  (2023)  Modulation effect of black rice dietary fiber on the metabolism and fermentation of cyanidin-3-glucoside in an in vitro human colonic model.  Food & Function,  14  (14): (6707-6717).  [PMID:37404037] [10.1039/D3FO00955F]
25. Li Chao, Li Jiale, Huang Niu, Kong Xin Ying, Xiao Qingyi, Huang Yingping, Wong Po Keung, Ye Liqun.  (2023)  Ultrastable Co-NC membrane for sterilization of Escherichia coli in flowing water.  npj Clean Water,  (1): (1-11).  [PMID:] [10.1038/s41545-023-00259-5]
26. Ya-Ling Tang, Guan-Qi Zheng, Yu-Xin Lin, Peng Lu, Hai-Bo Zhao, De-Ming Guo, Li Chen, Bo-Wen Liu, Yu-Zhong Wang.  (2023)  Bio-based long-chain aliphatic polyamide with intrinsic flame retardancy and great overall properties.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2023.110416]
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227. Xinke Li, Xinru Wang, Xing Wang, Hanwen Xin, Xujie Yang, Jinghui Zhou, Dayin Sun.  (2024)  Lignin-Decorated SiO2 Nanoparticles for Skin Cleansing Applications.  ACS Applied Nano Materials,      [PMID:] [10.1021/acsanm.3c05263]
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230. Huaimin Wang, Shuang Meng, Zixuan Zhang, Chenying Zhou, Heng Zhang, Yang Liu, Chuan-shu He, Peng Zhou, Bo Lai.  (2024)  Mechanical agitation and ultrasound constructed in situ Fenton system: The role of atomic hydrogen for Fe(III) reduction.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.126859]
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233. Min He, Yidong Bin, Lixian Huang, Caiying Li, Yuzhen Ma, Yan-Ni Luo, Shulin Zhao, Jinzhe Liang.  (2025)  Novel zinc(II) phthalocyanine nanoparticles as diagnosis-treatment nanoprobe for photoacoustic imaging-guided synergistic photothermal/photodynamic-enhanced cancer therapy.  Inorganic Chemistry Frontiers,      [PMID:] [10.1039/D4QI02898H]
234. Peng Zhang, Minglu Sun, Chenying Zhou, Chuan-Shu He, Yang Liu, Heng Zhang, Zhaokun Xiong, Wen Liu, Peng Zhou, Bo Lai.  (2024)  Origins of Selective Oxidation in Carbon-Based Nonradical Oxidation Processes toward Organic Pollutants: Quantitative Structure–Activity Relationships (QSARs).  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:38410972] [10.1021/acs.est.3c06252]
235. Hengyi Fu, Wenxiao Zheng, Weijian Duan, Guodong Fang, Xiaoguang Duan, Shaobin Wang, Chunhua Feng, Shishu Zhu.  (2024)  Overlooked Roles and Transformation of Carbon-Centered Radicals Produced from Natural Organic Matter in a Thermally Activated Persulfate System.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:39126387] [10.1021/acs.est.4c06770]
236. Ullah Saif, Liao Chengrui, Xu Yuanyuan, Li Wannian, Ali Izhar, Han Xiaomei, Ye Shaoming, Yang Mei.  (2024)  Phenolic Acid Concentration and Adsorption in the Soil of Monoculture Eucalyptus and Acacia Mangium Plantations Versus Species Mixtures in Subtropical Forests.  Journal of Soil Science and Plant Nutrition,      [PMID:] [10.1007/s42729-024-01794-x]
237. Xintong Li, Baocheng Qu, Jingyao Wang, Hongxia Zhao.  (2024)  Phototransformation of tetrabromobisphenol A bis (allyl ether) in an aqueous solution: Role of environmentally persistent free radicals.  CHEMOSPHERE,      [PMID:39293686] [10.1016/j.chemosphere.2024.143342]
238. Weidong Li, Haichao Li, Lin Luo, Sen Ma, Renjie Huang, Zheng Li, Lu Lin, Xianhai Zeng.  (2025)  Precise fractionation of hemicellulose from bamboo biomass achieved with renewable bifunctional 4-hydroxybenzoic acid stabilizing lignin βO4 bonds.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.132455]
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