Ferulic Acid Ethyl Ester - ≥97% , CAS No.4046-02-0

CAS: 4046-02-0 Cat. No.: F104905 Molecular Weight: 222.24 Beilstein Registry Number: 10(4)1780 EC Number: 223-745-5
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
AKOS015889646 | NSC14879 | NSC-14879 | Ethyl ferulate - Natural grade | NSC 14879 | ethyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | BCP15347 | F-2010 | Ethyl (2e)-3-(4-Hydroxy-3-Methoxyphenyl)prop-2-Enoate | MFCD00009190 | ethyl 3-(4-hydroxy-3-methoxyp
Storage
Protected from light,Argon charged,Room temperature
Shipped In
Normal
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1g
F104905-1g
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5g
F104905-5g
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F104905-25g
4

$18.90

$28.90
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100g
F104905-100g
3

$69.90

$104.90
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500g
F104905-500g
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Why this grade

≥97% 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 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Ethyl ferulate, a naturally lipophilic derivative of ferulic acid originally derived from Rhizoma Chuanxiong, induces heme oxygenase-1 (HO-1) and protects rat neurons against oxidative stress[1]. Ethyl ferulate also protects neurons against amyloid β peptide (1-42)-induced oxidative stress and neurotoxicity

Specifications

Synonyms
AKOS015889646 | NSC14879 | NSC-14879 | Ethyl ferulate - Natural grade | NSC 14879 | ethyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | BCP15347 | F-2010 | Ethyl (2e)-3-(4-Hydroxy-3-Methoxyphenyl)prop-2-Enoate | MFCD00009190 | ethyl 3-(4-hydroxy-3-methoxyp
Specifications & Purity
≥97%
Storage
Protected from light, Argon charged, Room temperature
Shipped In
Normal
Purity
≥97%
Names and Identifiers
Pubchem Sid488191369
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488191369
Canonical SmilesCCOC(=O)C=CC1=CC(=C(C=C1)O)OC
IUPAC Nameethyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
InChIKeyATJVZXXHKSYELS-FNORWQNLSA-N
INCHI1S/C12H14O4/c1-3-16-12(14)7-5-9-4-6-10(13)11(8-9)15-2/h4-8,13H,3H2,1-2H3/b7-5+
Isomeric SMILES CCOC(=O)/C=C/C1=CC(=C(C=C1)O)OC
WGK Germany 3
Molecular Weight 222.24
Beilstein 10(4)1780
Reaxy-Rn 2696806
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2696806&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
SuperclassPhenylpropanoids and polyketides
ClassCinnamic acids and derivatives
SubclassHydroxycinnamic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentCoumaric acids and derivatives
Alternative Parents Cinnamic acid esters  Methoxyphenols  Styrenes  Phenoxy compounds  Methoxybenzenes  Anisoles  Fatty acid esters  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  Enoate esters  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Coumaric acid or derivatives - Cinnamic acid ester - Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Styrene - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Fatty acid ester - Phenol - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Ether - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organooxygen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3B Tclin Glycogen synthase kinase-3 beta (11785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGM2 Tchem Protein-glutamine gamma-glutamyltransferase (1221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Calu-1 (518 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 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
MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-N-SH (1499 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1299 (3248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H157 (619 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 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
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1792 (313 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Glo1 Glyoxalase I (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Athelia rolfsii (768 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.

16 results found

Lot NumberCertificate TypeDateItem
F2610077Certificate of AnalysisSep 19, 2025 F104905
J2509366Certificate of AnalysisSep 19, 2025 F104905
J2509367Certificate of AnalysisSep 19, 2025 F104905
J2509368Certificate of AnalysisSep 19, 2025 F104905
J2509369Certificate of AnalysisSep 19, 2025 F104905
J2509370Certificate of AnalysisSep 19, 2025 F104905
C2520230Certificate of AnalysisMar 29, 2025 F104905
F2102286Certificate of AnalysisMar 04, 2025 F104905
F2102287Certificate of AnalysisMar 04, 2025 F104905
K2504414Certificate of AnalysisJun 21, 2024 F104905
B2019070Certificate of AnalysisDec 18, 2023 F104905
L1906105Certificate of AnalysisSep 07, 2023 F104905
F2102273Certificate of AnalysisJun 15, 2021 F104905
G2313126Certificate of AnalysisJun 15, 2021 F104905
G2313135Certificate of AnalysisJun 15, 2021 F104905
G2313128Certificate of AnalysisMay 06, 2021 F104905

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Chemical and Physical Properties
SolubilitySoluble in Methanol
SensitivityLight sensitive.
Boil Point(°C)185°C
Melt Point(°C)57°C
Molecular Weight222.240 g/mol
XLogP32.200
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass222.089 Da
Monoisotopic Mass222.089 Da
Topological Polar Surface Area55.800 Ų
Heavy Atom Count16
Formal Charge0
Complexity249.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. 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]
2. Jian Yao, Lun Gui, Qizhang Long.  (2022)  A chlorogenic acid esterase from a metagenomic library with unique substrate specificity and its application in caffeic and ferulic acid production from agricultural byproducts.  BIOCATALYSIS AND BIOTRANSFORMATION,      [PMID:] [10.1080/10242422.2021.1969370]
3. Xiaoxiao Wei, Yuanyuan Yu, Zheng Shen, Yi Liu, Xi Liu, Shuangfei Wang, Liming Zhang, Douyong Min.  (2022)  Deciphering the linkage type and structural characteristics of the p-hydroxyphenyl unit in Pinus massoniana Lamb compressed wood lignin.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:35367267] [10.1016/j.ijbiomac.2022.03.181]
4. Ni Shuzhen, Liu Na, Fu Yingjuan, Gao Hailong, Qin Menghua.  (2021)  Laccase mediated phenol/chitosan treatment to improve the hydrophobicity of Kraft pulp.  CELLULOSE,  28  (7): (4397-4409).  [PMID:] [10.1007/s10570-021-03766-1]
5. Teng Sun, Haiping Zhang, Zhe Dong, Zengshe Liu, Mingming Zheng.  (2020)  Ultrasonic-promoted enzymatic preparation, identification and multi-active studies of nature-identical phenolic acid glycerol derivatives.  RSC Advances,  10  (19): (11139-11147).  [PMID:35495308] [10.1039/C9RA09830E]
6. Haiping Zhang, Mingming Zheng, Jie shi, Hu Tang, Qianchun Deng, Fenghong Huang, Dan Luo.  (2017)  Enzymatic preparation of “functional oil” rich in feruloylated structured lipids with solvent-free ultrasound pretreatment.  FOOD CHEMISTRY,      [PMID:29329854] [10.1016/j.foodchem.2017.12.069]
7. Chunfang Xu, Haiping Zhang, Jie Shi, Mingming Zheng, Xia Xiang, Fenghong Huang, Junyong Xiao.  (2017)  Ultrasound irradiation promoted enzymatic alcoholysis for synthesis of monoglyceryl phenolic acids in a solvent-free system.  ULTRASONICS SONOCHEMISTRY,      [PMID:29137734] [10.1016/j.ultsonch.2017.09.016]
8. Jian-yong Zheng, Jian Wang, Sha-sha Zhou, Xiao-jun Li, Xiang-xian Ying, Zhao Wang.  (2015)  A stereoselective esterase from Bacillus megaterium: Purification, gene cloning, expression and catalytic properties.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:26518366] [10.1016/j.pep.2015.10.001]
9. Wen-hua Tong, Shu-qin Wang, Guan-ying Chen, Dong-xu Li, Yan-sen Wang, Li-ming Zhao, Ying Yang.  (2024)  Characterization of the structural and molecular interactions of Ferulic acid ethyl ester with human serum albumin and Lysozyme through multi-methods.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38870694] [10.1016/j.saa.2024.124549]
10. Tian Tian, Yu Peng, Shuangyang Chen, Yue Zhang, Yi Li, Aonan Xia, Erhu Li, Xuedan Cao.  (2026)  Screening of a feruloyl esterase-producing lactobacillus strain and its application in citrus whole-fruit pulp fermentation: organic acids, volatile compounds, and sensory evaluation.  FOOD RESEARCH INTERNATIONAL,      [PMID:41703864] [10.1016/j.foodres.2026.118410]
11. Zhang Xinyu, Li Yijie, Lin Hong, He Junbo, Feng Jiangtao, Cai Meng.  (2026)  Enzymatic Synthesis, Characterization, Antioxidant Activity, and Density Functional Theory Calculation of Novel 1-O-alkylglyceryl Ferulate.  Food Biophysics,  21  (1): (17).  [PMID:] [10.1007/s11483-026-10106-y]
Solution Calculators
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