Determine the necessary mass, volume, or concentration for preparing a solution.
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≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Pinostilbene (trans-Pinostilbene) is a major metabolite of Pterostilbene.
| Pubchem Sid | 504763857 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504763857 |
| Sourires canoniques | COC1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O |
| IUPAC Name | 3-[(E)-2-(4-hydroxyphenyl)ethenyl]-5-methoxyphenol |
| InChIKey | KUWZXOMQXYWKBS-NSCUHMNNSA-N |
| INCHI | 1S/C15H14O3/c1-18-15-9-12(8-14(17)10-15)3-2-11-4-6-13(16)7-5-11/h2-10,16-17H,1H3/b3-2+ |
| Isomères SMILES | COC1=CC(=CC(=C1)O)/C=C/C2=CC=C(C=C2)O |
| PubChem CID | 5473050 |
| Poids moléculaire | 242.27 |
| Reaxy-Rn | 1879704 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Classe | Stilbenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Stilbenes |
| Alternative Parents | Methoxyphenols Styrenes Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Stilbene - Methoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Styrene - Phenol ether - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Benzenoid - Monocyclic benzene moiety - Ether - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. |
| External Descriptors | stilbenol |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
| Certificate of Analysis | Sep 08, 2025 | P160115 | |
| Certificate of Analysis | Sep 08, 2025 | P160115 | |
| Certificate of Analysis | Sep 08, 2025 | P160115 | |
| Certificate of Analysis | Sep 08, 2025 | P160115 | |
| Certificate of Analysis | Apr 08, 2024 | P160115 | |
| Certificate of Analysis | Apr 08, 2024 | P160115 | |
| Certificate of Analysis | Apr 08, 2024 | P160115 | |
| Certificate of Analysis | Apr 08, 2024 | P160115 |
| Sensibilité | Light&Air&Heat sensitive |
|---|---|
| Point de fusion (°C) | 117.0 to 121.0 °C |
| Poids moléculaire | 242.270 g/mol |
| XLogP3 | 3.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 242.094 Da |
| Monoisotopic Mass | 242.094 Da |
| Topological Polar Surface Area | 49.700 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 269.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
| 1. Ming Su, Lei Ye, Yunbing Tang, Shaowei Wang, Zhiyan Hu, Huitao Li, Yiyan Wang, Xiaoheng Li, Yi Liu, Ren-Shan Ge. (2023) Inhibition of Resveratrol Analogs on Human and Rat 3β-Hydroxysteroid Dehydrogenases: Structure–Activity Relationship and Docking Analysis. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:37129992] [10.1021/acs.jafc.3c01919] |
| 2. C. Hu, Y. Zhai, H. Lin, H. Lu, J. Zheng, C. Wen, X. Li, R.S. Ge, Y. Liu, Q. Zhu. (2024) Resveratrol analogues and metabolites selectively inhibit human and rat 11β-hydroxysteroid dehydrogenase 1 as the therapeutic drugs: structure–activity relationship and molecular dynamics analysis. SAR AND QSAR IN ENVIRONMENTAL RESEARCH, [PMID:39139138] [10.1080/1062936X.2024.2389817] |