Ethylvanillin(NSC 1803) - Moligand™, ≥98% , CAS No.121-32-4

CAS: 121-32-4 Cat. No.: E107635 Molecular Weight: 166.17 Beilstein Registry Number: 1073761 EC Number: 204-464-7
AVAILABLE TO ORDER
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. ≥98%
Synonyms
AB00949623_05 | ETHYL VANILLIN [FCC] | NSC 1803 | Vanillal | CAS-121-32-4 | ETHYL VANILLIN [USP-RS] | ETHYL VANILLIN [WHO-DD] | SR-01000865052 | Vanillin, ethyl- | VANILLIN,ETHYL [VANDF] | A804713 | Arovanillon | BBL023011 | s4568 | NCGC00256500-01 | SY01
Storage
Protected from light,Argon charged,Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
25g
E107635-25g
7

$10.90

$16.90
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100g
E107635-100g
9

$14.90

$22.90
Save $8.00 (34.93%)
500g
E107635-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$42.90

$64.90
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Why this grade

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

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Storage & shipping

Protected from light,Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 32 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

It plays an important role as an antioxidant and is also used as a flavoring agent, in perfumes, and in organic synthesis. It holds anti-angiogenic, anti-inflammatory and antinociceptive properties.

Specifications

Synonyms
AB00949623_05 | ETHYL VANILLIN [FCC] | NSC 1803 | Vanillal | CAS-121-32-4 | ETHYL VANILLIN [USP-RS] | ETHYL VANILLIN [WHO-DD] | SR-01000865052 | Vanillin, ethyl- | VANILLIN, ETHYL [VANDF] | A804713 | Arovanillon | BBL023011 | s4568 | NCGC00256500-01 | SY01
Specifications & Purity
Moligand™, ≥98%
Storage
Protected from light, Argon charged, Room temperature
Shipped In
Normal
Grade
Moligand™
Purity
≥98%
Names and Identifiers
Pubchem Sid488180803
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180803
Canonical SmilesCCOC1=C(C=CC(=C1)C=O)O
IUPAC Name3-ethoxy-4-hydroxybenzaldehyde
InChIKeyCBOQJANXLMLOSS-UHFFFAOYSA-N
INCHI1S/C9H10O3/c1-2-12-9-5-7(6-10)3-4-8(9)11/h3-6,11H,2H2,1H3
Isomeric SMILES CCOC1=C(C=CC(=C1)C=O)O
WGK Germany 3
RTECS CU6125000
Molecular Weight 166.17
Beilstein 1073761
Reaxy-Rn 1073761
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1073761&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
SuperclassOrganic oxygen compounds
ClassOrganooxygen compounds
SubclassCarbonyl compounds
Intermediate Tree Nodes Aldehydes - Aryl-aldehydes - Benzaldehydes
Direct ParentHydroxybenzaldehydes
Alternative Parents Phenoxy compounds  Phenol ethers  Benzoyl derivatives  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Hydroxybenzaldehyde - Phenoxy compound - Phenol ether - Benzoyl - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Ether - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
External Descriptors aromatic ether - phenols - benzaldehydes
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAKI-1 (44928 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KM12 (47707 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M14 (47487 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-3 (48710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-8 (47708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-5 (47095 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SN12C (47755 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
Lymphoblastoid cell (5959 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
Malme-3M (44254 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 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.

17 results found

Lot NumberCertificate TypeDateItem
C2212320Certificate of AnalysisDec 10, 2025 E107635
I2509384Certificate of AnalysisAug 29, 2025 E107635
I2509383Certificate of AnalysisAug 29, 2025 E107635
I2509326Certificate of AnalysisAug 29, 2025 E107635
C2604013Certificate of AnalysisAug 29, 2025 E107635
I2509325Certificate of AnalysisAug 29, 2025 E107635
G2415616Certificate of AnalysisApr 29, 2024 E107635
G2415612Certificate of AnalysisApr 29, 2024 E107635
G2415608Certificate of AnalysisApr 29, 2024 E107635
F2506489Certificate of AnalysisApr 29, 2024 E107635
C2212255Certificate of AnalysisFeb 18, 2022 E107635
D2310315Certificate of AnalysisFeb 18, 2022 E107635
D2310304Certificate of AnalysisFeb 18, 2022 E107635
C2507110Certificate of AnalysisFeb 18, 2022 E107635
C2214186Certificate of AnalysisFeb 18, 2022 E107635
C2212323Certificate of AnalysisFeb 18, 2022 E107635
L2322041Certificate of AnalysisFeb 18, 2022 E107635

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Chemical and Physical Properties
SolubilitySlightly soluble in water. Soluble in ethanol, ether, benzene.
SensitivitySensitive to air; sensitive to light
Flash Point(°F)293 °F
Flash Point(°C)145 °C
Boil Point(°C)149-150°C
Melt Point(°C)78°C
Molecular Weight166.170 g/mol
XLogP31.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass166.063 Da
Monoisotopic Mass166.063 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count12
Formal Charge0
Complexity147.000
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. Yurong Zhuang, Chenchen Wang, Yong Wang, Yuhui Chen, Songqin Liu, Wei Wei.  (2023)  Colorimetric and surface-enhanced Raman scattering method for vanillin detection based on two types of reduced silver nanoparticles.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2023.134267]
2. Chenghong Huang, Hong Tang, Xiaorong Huang, Hongjie Chen, Kang Yang, Qi Yin, Lin Zhang, Xia Li, Xue Mou, Shuangkou Chen, Yuchan Zhang, Yan Hu.  (2023)  Ethyl Vanillin Rapid Crystallization from Carboxymethyl Chitosan Ion-Switchable Hydrogels.  Gels,  (4): (335).  [PMID:37102947] [10.3390/gels9040335]
3. Zhentao Li, Zhengzheng Liao, Jinfang Hu, Zilin Chen.  (2023)  In situ growth of imine-based covalent organic framework as stationary phase for high-efficiency electrochromatographic separation.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:36881971] [10.1016/j.chroma.2023.463905]
4. Ruixue Yangcheng, Yuntong Cui, Shuang Luo, Jiansu Ran, Jianjian Wang.  (2023)  Hierarchical pore-trapped and hydrogen-bonded phosphoric acid in Pd-supported zeolite for the efficient aqueous hydrodeoxygenation of lignin derivatives at ambient temperature.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2023.112460]
5. Weichen Wang, Tian Sheng, Shanshuai Chen, Zhiyu Xiang, Fangyuan Zhou, Wanbin Zhu, Hongliang Wang.  (2022)  Defect engineering of Metal-Organic Framework for highly efficient hydrodeoxygenation of lignin derivates in water.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.139711]
6. Di Chen, Bin Wang, Xin-Li Xu, Man-Yu Zhang, Xin-Miao Bu, Sen Yang, Yanbo Luo, Xia Xu.  (2022)  Kapok fiber-supported liquid extraction for convenient oil samples preparations: A feasibility and proof-of-concept study.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:36095972] [10.1016/j.chroma.2022.463480]
7. Jiansu Ran, Ruixue YangCheng, Yuntong Cui, Jianjian Wang.  (2022)  Significant Promotion of Carboxyl Groups in Palladium Nanoparticles-Supported Biomass Carbon Catalysts for Efficient Low-Temperature Hydrodeoxygenation of Lignin Derivatives in Water.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.2c00572]
8. Li Minglei, Wang Dingzhong, Zhao Wuduo, Xi Hui, Xu Hengyi, Sun Shihao, Fu Yingjie, Zhang Shusheng, Mao Jian, Zhang Jianxun.  (2022)  Simultaneous determination of multiple flavorings in infant formula by direct analysis in real time-mass spectrometry.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2022.113586]
9. Zidan Zou, Chun Chen, Zhi Hu, Yue Shen, Zhen Fu, Wenchao Li, Yunxia Zhang, Haimin Zhang, Huijun Zhao, Guozhong Wang.  (2022)  Core shell hetero-structured SiO2@Ni/SiO2 catalyst for efficient aqueous-phase hydrogenation of bio-derived unsaturated compounds.  FUEL,      [PMID:] [10.1016/j.fuel.2022.123694]
10. Ruixue Yangcheng, Jiansu Ran, Zhaohui Liu, Yuntong Cui, Jianjian Wang.  (2022)  Phosphoric acid-modified commercial kieselguhr supported palladium nanoparticles as efficient catalysts for low-temperature hydrodeoxygenation of lignin derivatives in water.  GREEN CHEMISTRY,  24  (4): (1570-1577).  [PMID:] [10.1039/D1GC04243B]
11. Hao-Zhou Huang, Yue-Hua Cong, An Du, Bing Hu, Bao-Yan Zhang.  (2021)  Liquid crystalline dimers containing a cholesteryl group: chiral smectic phases and TGBA* phase.  LIQUID CRYSTALS,      [PMID:] [10.1080/02678292.2021.1900431]
12. Lu Xiaowen, Guo Chunmu, Zhang Mingyang, Leng Leipeng, Horton J. Hugh, Wu Wei, Li Zhijun.  (2021)  Rational design of palladium single-atoms and clusters supported on silicoaluminophosphate-31 by a photochemical route for chemoselective hydrodeoxygenation of vanillin.  Nano Research,  14  (11): (4347-4355).  [PMID:] [10.1007/s12274-021-3857-2]
13. Dongdong Wang, Wanbing Gong, Jifang Zhang, Miaomiao Han, Chun Chen, Yunxia Zhang, Guozhong Wang, Haimin Zhang, Huijun Zhao.  (2021)  Encapsulated Ni-Co alloy nanoparticles as efficient catalyst for hydrodeoxygenation of biomass derivatives in water.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(21)63828-7]
14. Zhijun Li, Xiaowen Lu, Weiwei Sun, Leipeng Leng, Mingyang Zhang, Honghong Li, Lu Bai, Dundong Yuan, J. Hugh Horton, Qian Xu, Jun Wang.  (2021)  One-step synthesis of single palladium atoms in WO2.72 with high efficiency in chemoselective hydrodeoxygenation of vanillin.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2021.120535]
15. Jing Yang, Shijie Xu, Jingkang Wang, Junbo Gong.  (2020)  Nucleation behavior of ethyl vanillin: Balance between chemical potential difference and saturation temperature.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2020.112609]
16. Xin Fu, Dongliang Zhu, Lan Huang, Xiangyang Yan, Shaomin Liu, Chenghui Wang.  (2019)  Superparamagnetic core-shell dummy template molecularly imprinted polymer for magnetic solid-phase extraction of food additives prior to the determination by HPLC.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2019.104169]
17. Fanyong Yan, Xiaodong Sun, Ruiqi Zhang, Yingxia Jiang, Jinxia Xu, Junfu Wei.  (2019)  Enhanced fluorescence probes based on Schiff base for recognizing Cu2+ and effect of different substituents on spectra.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:31174152] [10.1016/j.saa.2019.117222]
18. Li-Xian Zhu, Qin-Bao Lin, Jia-Yi Li, Hong-Mei Zhu, Hong-Sheng Ma, Huai-Ning Zhong, Jing-Jing Pan.  (2019)  Sources of potassium permanganate consumption for food contact paper.  Food Packaging and Shelf Life,      [PMID:] [10.1016/j.fpsl.2019.100319]
19. Rui Xiao, Xiaoting Zhang, Xiaona Zhang, Jiahua Niu, Minghua Lu, Xiuhua Liu, Zongwei Cai.  (2017)  Analysis of flavors and fragrances by HPLC with Fe3O4@GO magnetic nanocomposite as the adsorbent.  TALANTA,      [PMID:28213232] [10.1016/j.talanta.2017.01.065]
20. Hao Wu, Jingkang Wang, Yanan Zhou, Nannan Guo, Qi Liu, Shuyi Zong, Ying Bao, Hongxun Hao.  (2016)  Solid–liquid phase equilibrium and dissolution properties of ethyl vanillin in pure solvents.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2016.10.029]
21. Jingying Pan, Jie Fu, Shuguang Deng, Xiuyang Lu.  (2015)  Distribution coefficient of products from lignin oxidative degradation in organic-water systems.  FUEL PROCESSING TECHNOLOGY,      [PMID:] [10.1016/j.fuproc.2015.09.016]
22. Kissa R. Alunga, Yue-Yuan Ye, Shui-Rong Li, Duo Wang, Yun-Quan Liu.  (2015)  Catalytic oxidation of lignin–acetoderivatives: a potential new recovery route for value-added aromatic aldehydes from acetoderivatives.  Catalysis Science & Technology,  (7): (3746-3753).  [PMID:] [10.1039/C5CY00419E]
23. Detao Li, Zichen Ning, Zhuoshan Gong, Limin Zhou, Li Xu, Feiqiang He, Hamza Shehzad, Heng Jerry, Shichao Du, Jinbo Ouyang.  (2025)  Insights into salts/cocrystals formation of polyhydroxy natural products as well as their separation behavior via cocrystallization.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.131453]
24. Peng Qiannan, Zhao Cheng, Wang Xiaopeng, Cheng Kelin, Wang Congcong, Xu Xihui, Lin Lu.  (2025)  Modeling bacterial interactions uncovers the importance of outliers in the coastal lignin-degrading consortium.  Nature Communications,  16  (1): (1-13).  [PMID:39809803] [10.1038/s41467-025-56012-8]
25. Hongyu Qu, Xiangcheng Li, Xiao Han, Junjie Li, Xinqiang Feng, Chuang Liu, Zhendong Wang, Weimin Yang.  (2024)  Ni-Supported Germanosilicate Zeolite SCM-14 for Efficient Hydrogenolysis of 5-Hydroxymethylfurfural to 2,5-Dimethylfuran.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.4c03041]
26. Xuerui Lou, Minglei Li, Weiwei Guo, Yingjie Fu, Hui Xi, Peng Li, Wuduo Zhao, Shihao Sun.  (2024)  Rapid Determination of Flavorings in e-Cigarette Liquid by Direct Analysis in Real Time (DART) Mass Spectrometry (MS) in the Quick Strip Mode.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2024.2308054]
27. Zhang Hongtao, Gao Jiahui, Tan Lian, Zheng Li, Wang Longjie.  (2024)  Research on the Application of Terahertz Technology in Detecting Additives in Milk Powder.  Food Analytical Methods,      [PMID:] [10.1007/s12161-024-02720-8]
28. Jun Wu, Liqian Liu, Xinyue Yan, Gang Pan, Jiahao Bai, Chengbing Wang, Fuwei Li, Yong Li.  (2025)  Microenvironment engineering of nitrogen-doped hollow carbon spheres encapsulated with Pd catalysts for highly selective hydrodeoxygenation of biomass-derived vanillin in water.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(24)60261-5]
29. Zhenkun Mao, Changjun Hu, Zhentao Li, Zilin Chen.  (2019)  A reversed-phase/hydrophilic bifunctional interaction mixed-mode monolithic column with biphenyl and quaternary ammonium stationary phases for capillary electrochromatography.  ANALYST,  144  (14): (4386-4394).  [PMID:31210197] [10.1039/C9AN00428A]
30. Qunfeng Chen, Daobin Tang, Qi Zhang, Zhiyuan Tang, Longlong Ma, Xinghua Zhang.  (2025)  Electron-metal support interactions enhanced by W-O-Zr interface in Pd-UiO-66 catalyst for efficient HDO of lignin derivatives at room temperature.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.163903]
31. Feng He, Lingling Guo, Liqiang Liu, Xinxin Xu, Liguang Xu, Chuanlai Xu, Hua Kuang, Maozhong Sun.  (2025)  Highly Specific Monoclonal Antibodies Combined with A Multiplex Quantum Dot Microsphere-based Fluorescence Lateral Flow Immunochromatographic Assay for Simultaneous Detection of Vanillin, Methyl Vanillin, and Ethyl Vanillin in Food Samples.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:41147867] [10.1021/acs.jafc.5c09933]
32. Tianyin Huang, Yifan Yu, Wentao Zhang, Yue Zhao, Yiliang Tao, Wenguang Huang, Bingdang Wu.  (2026)  Molecular orbital-guided design of laccase–mediator systems for antibiotic removal in the presence of humic acid.  BIORESOURCE TECHNOLOGY,      [PMID:41513177] [10.1016/j.biortech.2026.133957]
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