2-(4-Hydroxyphenyl)ethanol - 10mM in DMSO , CAS No.501-94-0

CAS: 501-94-0 Cat. No.: H424324 Molecular Weight: 138.16 Beilstein Registry Number: 1859884 EC Number: 207-930-8
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GRADE & PURITY 10mM in DMSO
Synonyms
HYDROXYPHENETHYL ALCOHOL, P- | MLS001332424 | 1AK4MU3SNX | C06044 | SCHEMBL10620528 | bmse000173 | EN300-116733 | .beta.-(4-Hydroxyphenyl)ethanol | MFCD00002902 | 2-(4-Hydroxyphenyl)ethanol | 2-(4-hydroxyphenyl)-ethanol | Tyrosol | beta-(4-Hydroxyphenyl)e
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
H424324-1ml
1
$42.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 21 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

2-(4-Hydroxyphenyl)ethanol is a phenolic compound present in olives, which can exhibit a wide range of health benefits and pharmacological properties like anti-inflammatory, antiviral, anti-tumor and cardioprotection activity.

Specifications

Synonyms
HYDROXYPHENETHYL ALCOHOL, P- | MLS001332424 | 1AK4MU3SNX | C06044 | SCHEMBL10620528 | bmse000173 | EN300-116733 | .beta.-(4-Hydroxyphenyl)ethanol | MFCD00002902 | 2-(4-Hydroxyphenyl)ethanol | 2-(4-hydroxyphenyl)-ethanol | Tyrosol | beta-(4-Hydroxyphenyl)e
Specifications & Purity
10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
INHIBITOR
Names and Identifiers
Canonical SmilesC1=CC(=CC=C1CCO)O
IUPAC Name4-(2-hydroxyethyl)phenol
InChIKeyYCCILVSKPBXVIP-UHFFFAOYSA-N
INCHI1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2
Isomeric SMILES C1=CC(=CC=C1CCO)O
WGK Germany 3
Molecular Weight 138.16
Beilstein 1859884
Reaxy-Rn 1859884
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1859884&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.

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📊 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
ClassPhenols
SubclassTyrosols and derivatives
Intermediate Tree Nodes Not available
Direct ParentTyrosols
Alternative Parents 1-hydroxy-2-unsubstituted benzenoids  Benzene and substituted derivatives  Primary alcohols  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Tyrosol - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as tyrosols. These are organic aromatic compounds containing a phenethyl alcohol moiety that carries a hydroxyl group at the 4-position of the benzene group.
External Descriptors an aromatic compound
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 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
MET Tclin Hepatocyte growth factor receptor (10718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF-10A (2462 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-468 (9477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MM96L (154 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
SH-SY5Y (11521 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SW480 (6023 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NTRK2 Tclin Neurotrophic tyrosine kinase receptor type 2 (3279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Spinacia oleracea (250 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Choristoneura fumiferana (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
N2a (708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-12 (7051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mtcA1 Uncharacterized protein Rv1284/MT1322 (182 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PROBABLE TRANSMEMBRANE CARBONIC ANHYDRASE (CARBONATE DEHYDRATASE) (CARBONIC DEHYDRATASE) (107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAN2 Carbonic anhydrase 2 (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Verticillium dahliae (119 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:
Chemical and Physical Properties
Boil Point(°C)310°C
Melt Point(°C)90-95°C
Molecular Weight138.160 g/mol
XLogP30.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass138.068 Da
Monoisotopic Mass138.068 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count10
Formal Charge0
Complexity85.300
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
Citations of This Product
References
1. Chenchen Zhao, Yu Sha, Wei Zhuang, Yuan Rao, Jihang Zhang, Jinglan Wu, Tao Shen, Zhuotao Tan, Chenjie Zhu, Hongman Zhang, Hanjie Ying.  (2023)  Production of hydroxytyrosol from tyrosol via controllable oxidation with immobilized tyrosinase: A comparative study.  PROCESS BIOCHEMISTRY,      [PMID:] [10.1016/j.procbio.2023.06.017]
2. Tong Sun, Yan Liu, Ke Wang, Feiyu Duan, Lili Lu.  (2023)  Biotransformation of Tyrosol into a Novel Valuable α-Galactoside with Increased Solubility and Improved Anti-inflammatory Activities.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:37319317] [10.1021/acs.jafc.3c02529]
3. Jue Chen, Qibin Cheng, Qianqian Ma, Yuqi Wu, Liwei Zhang.  (2023)  Salidroside synthesis via glycosylation by β-D-glucosidase immobilized on chitosan microspheres in deep eutectic solvents.  BIOCATALYSIS AND BIOTRANSFORMATION,      [PMID:] [10.1080/10242422.2023.2178308]
4. Fengxia Tang, Chuan Li, Xiaoran Yang, Jiandu Lei, Hongxia Chen, Changwei Zhang, Chengzhang Wang.  (2022)  Effect of Variety and Maturity Index on the Physicochemical Parameters Related to Virgin Olive Oil from Wudu (China).  Foods,  12  (1): (7).  [PMID:36613224] [10.3390/foods12010007]
5. Jinbin Liu, Kaipeng Wang, Mian Wang, Huaxiang Deng, Xiaodong Chen, Yueling Shang, Xiaochen Liu, Xiaohong Yu.  (2022)  Efficient whole cell biotransformation of tyrosol from L-tyrosine by engineered Escherichia coli.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:35872508] [10.1016/j.enzmictec.2022.110100]
6. Li Jiang, Yanling Xiong, Yu Tu, Wentong Zhang, Qiyun Zhang, Peng Nie, Xiaojun Yan, Hongning Liu, Ronghua Liu, Guoliang Xu.  (2022)  Elucidation of the Transport Mechanism of Puerarin and Gastrodin and Their Interaction on the Absorption in a Caco-2 Cell Monolayer Model.  MOLECULES,  27  (4): (1230).  [PMID:35209020] [10.3390/molecules27041230]
7. Xu Yu, Li Yu, Fei Ma, Peiwu Li.  (2020)  Quantification of phenolic compounds in vegetable oils by mixed-mode solid-phase extraction isotope chemical labeling coupled with UHPLC-MS/MS.  FOOD CHEMISTRY,      [PMID:32721834] [10.1016/j.foodchem.2020.127572]
8. Wenjing Li, Congyong Sun, Wenwen Deng, Yingkun Liu, Michael Adu-Frimpong, Jiangnan Yu, Ximing Xu.  (2019)  Pharmacokinetic of gastrodigenin rhamnopyranoside from Moringa seeds in rodents.  FITOTERAPIA,      [PMID:31470062] [10.1016/j.fitote.2019.104348]
9. Jiahong Han, Min Dai, Yan Zhao, Enbo Cai, Lianxue Zhang, Xiaohuan Jia, Nian Sun, Xuan Fei, Hui Shu.  (2019)  Compatibility effects of ginseng and Ligustrum lucidum Ait herb pair on hematopoietic recovery in mice with cyclophosphamide-induced myelosuppression and its material basis.  Journal of Ginseng Research,      [PMID:32148411] [10.1016/j.jgr.2019.01.001]
10. Zhihua Liao, Fei Qiu, Junlan Zeng, Li Gu, Bangjun Wang, Xiaozhong Lan, Min Chen.  (2018)  A Novel UDP-Glycosyltransferase of Rhodiola crenulata Converts Tyrosol to Specifically Produce Icariside D2.  Biomed Research International,      [PMID:30027099] [10.1155/2018/7970590]
11. Xianglai Li, Zhenya Chen, Yifei Wu, Yajun Yan, Xinxiao Sun, Qipeng Yuan.  (2018)  Establishing an Artificial Pathway for Efficient Biosynthesis of Hydroxytyrosol.  ACS Synthetic Biology,      [PMID:29281883] [10.1021/acssynbio.7b00385]
12. Zhihong Wang, Chengzhang Wang, Changwei Zhang, Wenjun Li.  (2017)  Ultrasound-assisted enzyme catalyzed hydrolysis of olive waste and recovery of antioxidant phenolic compounds.  Innovative Food Science & Emerging Technologies,      [PMID:] [10.1016/j.ifset.2017.02.013]
13. Zhuang Yibin, Jiang Jingjie, Bi Huiping, Yin Hua, Liu Shaowei, Liu Tao.  (2015)  Synthesis of rosmarinic acid analogues in Escherichia coli.  BIOTECHNOLOGY LETTERS,  38  (4): (619-627).  [PMID:26667131] [10.1007/s10529-015-2011-1]
14. Yanhong BI, Zhaoyu WANG, Yanyong MAO, Shangyong ZHENG, Haijiang ZHANG, Hao SHI.  (2012)  Ionic Liquid Effects on the Activity of β-Glycosidase for the Synthesis of Salidroside in Co-solvent Systems.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(11)60395-1]
15. Yuqi Liu, Li Yuan, Guozheng Liang, Aijuan Gu.  (2024)  Preparation of Thermally Resistant and Mechanically Strong Biomass Benzoxazine Resins via Green Strategy.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.3c06195]
16. Jishan Li, Muyang Li, Chenyu Yong, Zhemin Zhou, Laichuang Han, Zhongmei Liu.  (2025)  Reshaping UDP-binding pocket of bacterial sucrose synthase to improve efficiency of UDP-glucose production.  BIORESOURCE TECHNOLOGY,      [PMID:40090494] [10.1016/j.biortech.2025.132396]
17. Yu Peng, Xiaoao Xiao, Tingting Ji, Xinyuan Wang, Yixuan Xu, Jianbo Xiao, Hui Cao, Zhiyong Chen, Huifan Liu, Yuanqing Gao, Hongxun Tao.  (2024)  Reveal the pharmacodynamic substances and mechanism of an edible medicinal plant Rhodiola crenulate in DSS-induced colitis through plasma pharmacochemistry and metabolomics.  Food Science and Human Wellness,      [PMID:] [10.26599/FSHW.2022.9250176]
18. Feng Lijuan, Yu Shuping, Jin Weimei, Xiao Changyan, Qiao Yan, Yang Guangfeng.  (2024)  The role of hydroponic solution of Ulva fasciata in modulating the antibiotic resistance of Vibrio alginolyticus.  JOURNAL OF APPLIED MICROBIOLOGY,      [PMID:39533112] [10.1093/jambio/lxae281]
19. Tong Sun, Jingyi Yang, Lili Lu.  (2025)  Glycosylation and sugar variations in tyrosol yield promising prebiotic-like effects.  Current Research in Food Science,      [PMID:41080798] [10.1016/j.crfs.2025.101206]
20. Siwen Li, Hongyan Zhu, Songtao Li, Rasmané SEMDE, Hongbo Teng, Mengqi Shi, Liang Huang, Xinru Lou, Beining Jia, Yan Zhao.  (2025)  Protocatechuic Acid improves Alzheimer's disease by regulating the cholinergic synaptic signaling pathway.  CHEMISTRY & BIODIVERSITY,      [PMID:39776239] [10.1002/cbdv.202402771]
21. Zhiyun Yang, Xiao Ding, Junbo Yang, Mehboob Hussain, Yanan Ruan, Xi Gao, Guoxing Wu.  (2025)  Phytotoxic Potential of Methyl 4-Hydroxyphenylacetate Against Ageratina adenophora (Spreng.): Mechanistic Insights and Implications for Sustainable Weed Management.  Agriculture-Basel,  15  (8):   [PMID:] [10.3390/agriculture15080824]
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