3,4-Dimethoxycinnamic acid - ≥99% , CAS No.2316-26-9

CAS: 2316-26-9 Cat. No.: D100558 Molecular Weight: 208.21 Beilstein Registry Number: 10(1)212 EC Number: 219-025-5
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Synonyms
3-(3,4-Dimethoxyphenyl)-2-propenoic acid, 9CI | 3',4'-dimethoxycinnamic acid | 3,4-DIMETHOXYCINNAMIC ACID | 3,4-dimethoxy-cinnamic acid | 7R-0613 | CCG-38678 | (E)-O-Methylferulic acid | NCGC00095522-03 | W-107420 | BVZ841PVJL | DTXSID501016475 | HMS2268F
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5g
D100558-5g
8

$9.90

$14.90
Save $5.00 (33.56%)
25g
D100558-25g
8

$30.90

$46.90
Save $16.00 (34.12%)
100g
D100558-100g
8

$73.90

$110.90
Save $37.00 (33.36%)
500g
D100558-500g
2

$188.90

$283.90
Save $95.00 (33.46%)
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Why this grade

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

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Storage & shipping

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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
3-(3, 4-Dimethoxyphenyl)-2-propenoic acid, 9CI | 3', 4'-dimethoxycinnamic acid | 3, 4-DIMETHOXYCINNAMIC ACID | 3, 4-dimethoxy-cinnamic acid | 7R-0613 | CCG-38678 | (E)-O-Methylferulic acid | NCGC00095522-03 | W-107420 | BVZ841PVJL | DTXSID501016475 | HMS2268F
Specifications & Purity
≥99%
Storage
Room temperature
Shipped In
Normal
Purity
≥99%
Names and Identifiers
Pubchem Sid488191226
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488191226
Canonical SmilesCOC1=C(C=C(C=C1)C=CC(=O)O)OC
IUPAC Name(E)-3-(3,4-dimethoxyphenyl)prop-2-enoic acid
InChIKeyHJBWJAPEBGSQPR-GQCTYLIASA-N
INCHI1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4+
Isomeric SMILES COC1=C(C=C(C=C1)/C=C/C(=O)O)OC
WGK Germany 3
Molecular Weight 208.21
Beilstein 10(1)212
Reaxy-Rn 1533435
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1533435&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.

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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
SuperclassPhenylpropanoids and polyketides
ClassCinnamic acids and derivatives
SubclassHydroxycinnamic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentCoumaric acids and derivatives
Alternative Parents Cinnamic acids  Dimethoxybenzenes  Styrenes  Phenoxy compounds  Anisoles  Alkyl aryl ethers  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Cinnamic acid - Coumaric acid or derivatives - O-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Anisole - Methoxybenzene - Styrene - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Ether - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Hydrocarbon derivative - 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 methoxycinnamic acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-1080 (3966 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PANC-1 (6144 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 2.2.15 (869 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Mapk1 MAP kinase ERK2 (650 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
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hepatitis B virus (7925 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RBL-2H3 (1162 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCT2 T-complex protein 1 subunit beta (5007 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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.

8 results found

Lot NumberCertificate TypeDateItem
F1820051Certificate of AnalysisJan 27, 2026 D100558
B2224298Certificate of AnalysisDec 10, 2025 D100558
B2224315Certificate of AnalysisDec 10, 2025 D100558
B2225123Certificate of AnalysisDec 10, 2025 D100558
F1820050Certificate of AnalysisApr 27, 2022 D100558
C2330957Certificate of AnalysisDec 16, 2021 D100558
C2330958Certificate of AnalysisDec 16, 2021 D100558
C2330961Certificate of AnalysisDec 16, 2021 D100558
Chemical and Physical Properties
Melt Point(°C)181-183°C
Molecular Weight208.210 g/mol
XLogP31.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass208.074 Da
Monoisotopic Mass208.074 Da
Topological Polar Surface Area55.800 Ų
Heavy Atom Count15
Formal Charge0
Complexity237.000
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
Citations of This Product
References
1. Xiaoxue Pan, Junyan Wei, Min Wang, Jie Zhang, Zhiming Xu, Haojie Wei, Nami Lai, Kainan Nian, Rui Zhang, Xuesheng Zhang.  (2023)  Comparative studies of transformation behaviors and mechanisms of halophenols in multiple chemical oxidative systems.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:36690111] [10.1016/j.scitotenv.2023.161756]
2. Xijuan Tu, Fengjie Yu, Qian Jin, Chunping Du, Jiaxu Chen, Ji Yang, Yuchang He, Shaokang Huang, Wenbin Chen.  (2022)  A Simple High-Throughput Field Sample Preparation Method Based on Matrix-Induced Sugaring-Out for the Simultaneous Determination of 5-Hydroxymethylfurfural and Phenolic Compounds in Honey.  MOLECULES,  27  (23): (8373).  [PMID:36500464] [10.3390/molecules27238373]
3. Wenjie Yu, Fengjie Sun, Ruixin Xu, Meng Cui, Yongquan Liu, Quanyuan Xie, Limin Guo, Chenxian Kong, Xin Li, Xiali Guo, Liping Luo.  (2022)  Chemical composition and anti-inflammatory activities of Castanopsis honey.  Food & Function,  14  (1): (250-261).  [PMID:36484340] [10.1039/D2FO02233H]
4. Denghao Ouyang, Hongmei Chen, Nan Liu, Jingzhi Zhang, Xuebing Zhao.  (2021)  Insight into the negative effects of lignin on enzymatic hydrolysis of cellulose for biofuel production via selective oxidative delignification and inhibitive actions of phenolic model compounds.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2021.12.036]
5. Fengjie Yu, Jianing Zhang, Yunmin Tao, Chunping Du, Wenchao Yang, Wenbin Chen, Xijuan Tu.  (2021)  High-throughput subzero-temperature assisted homogenous liquid-liquid extraction for the fast sample preparation of multiple phenolic compounds in propolis.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:34147873] [10.1016/j.jchromb.2021.122823]
6. Houmei Liu, Zhan Li, Makoto Takafuji, Hirotaka Ihara, Hongdeng Qiu.  (2017)  Octadecylimidazolium ionic liquid-modified magnetic materials: Preparation, adsorption evaluation and their excellent application for honey and cinnamon.  FOOD CHEMISTRY,      [PMID:28372166] [10.1016/j.foodchem.2017.02.080]
7. Houmei Liu, Xiaojing Liang, Xusheng Wang, Yong Guo, Xia Liu.  (2014)  Polyelectrolyte assembled graphene oxide coated silica composite as sorbent for solid-phase extraction of cinnamic acid and its derivatives.  RSC Advances,  (6): (4420-4427).  [PMID:] [10.1039/C4RA13331E]
8. Peiliang Xiao, Suoqin Zhang, Huayu Ma, Aijun Zhang, Xiaoli Lv, Liangyu Zheng.  (2013)  Stereoselective synthesis of caffeic acid amides via enzyme-catalyzed asymmetric aminolysis reaction.  JOURNAL OF BIOTECHNOLOGY,      [PMID:24056082] [10.1016/j.jbiotec.2013.09.004]
9. Yupei Sun, Yanhui Yi, Bingkang Wang, Jinrong Li, Feng Zhao, Jianzeng Xin, Sheng Liu.  (2026)  Design, synthesis and anti-tumor activation of β-carboline alkaloids derivatives from Picrasma quassioides.  FITOTERAPIA,      [PMID:] [10.1016/j.fitote.2026.107209]
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