≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
3,4-Dimethoxyphenol was used in the synthesis of: · 5,6-dimethoxy benzofuranone derivatives, multi-target anti Alzheimer compounds · 3,4-dimethoxyphenyl-β-D-glucopyranoside · 4-(but-2-enyloxy)-1,2-dimethoxybenzene · precursors for the synthesis of the 4H-chromenes
| Pubchem Sid | 488182219 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488182219 |
| Canonical Smiles | COC1=C(C=C(C=C1)O)OC |
| IUPAC Name | 3,4-dimethoxyphenol |
| InChIKey | SMFFZOQLHYIRDA-UHFFFAOYSA-N |
| INCHI | 1S/C8H10O3/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5,9H,1-2H3 |
| Isomeric SMILES | COC1=C(C=C(C=C1)O)OC |
| WGK Germany | 3 |
| Molecular Weight | 154.16 |
| Beilstein | 1366650 |
| Reaxy-Rn | 1366650 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1366650&ln= |
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 | Benzenoids |
| Class | Phenols |
| Subclass | Methoxyphenols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Methoxyphenols |
| Alternative Parents | Dimethoxybenzenes 4-alkoxyphenols Phenoxy compounds Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | O-dimethoxybenzene - Dimethoxybenzene - Methoxyphenol - 4-alkoxyphenol - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - 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 methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 C2323880 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323915 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323941 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323944 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323959 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323961 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323962 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| C2323963 | Certificate of Analysis | Sep 08, 2026 | D107922 |
| H2529087 | Certificate of Analysis | Sep 04, 2025 | D107922 |
| B2521187 | Certificate of Analysis | Jun 18, 2024 | D107922 |
| H1815038 | Certificate of Analysis | Jan 05, 2024 | D107922 |
| C2123097 | Certificate of Analysis | Dec 15, 2022 | D107922 |
| Solubility | Soluble in water. |
|---|---|
| Sensitivity | Light Sensitive |
| Boil Point(°C) | 167°C/14mmHg |
| Melt Point(°C) | 80°C |
| Molecular Weight | 154.160 g/mol |
| XLogP3 | 1.700 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 154.063 Da |
| Monoisotopic Mass | 154.063 Da |
| Topological Polar Surface Area | 38.700 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 116.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Baoyu Wang, Peng Zhou, Ximing Yan, Hu Li, Hongguo Wu, Zehui Zhang. (2023) Cooperative catalysis of Co single atoms and nanoparticles enables selective CAr−OCH3 cleavage for sustainable production of lignin-based cyclohexanols. Journal of Energy Chemistry, [PMID:] [10.1016/j.jechem.2022.12.020] |
