3,4-Dimethoxyphenol - ≥97% , CAS No.2033-89-8

CAS: 2033-89-8 Cat. No.: D107922 Summenformel: C8H10O3 Molekulargewicht: 154.16 Beilstein Registry Number: 1366650 EG-Nummer: 217-995-4
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GRADE & PURITY ≥97%
Synonyms
3,4-Bis(methyloxy)phenol | 3,4-Dimethoxyphenol, 97% | MFCD00008390 | UNII-38B43WCU83 | 3 pound not4-dimethoxyphenol | TS-02054 | AKOS005146109 | 3,4-DIMETHOXYPHENOL | 3,4-dimethoxy-phenol | SY017636 | 38B43WCU83 | Q-101910 | AE-508/42302277 | FT-0614348 |
Storage
Room temperature
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
1g
D107922-1g
—
5 Auf Lager

8,59€

12,93€
Speichern 4,34 € (33.56%)
5g
D107922-5g
3 Auf Lager
6 Auf Lager

16,40€

25,08€
Speichern 8,68 € (34.60%)
10g
D107922-10g
—
5 Auf Lager

31,15€

46,77€
Speichern 15,62 € (33.40%)
25g
D107922-25g
2 Auf Lager
4 Auf Lager

75,41€

113,59€
Speichern 38,18 € (33.61%)
100g
D107922-100g
—
1 Auf Lager

301,02€

452,01€
Speichern 150,99 € (33.40%)
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

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

Übersicht

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

Specifications

Synonyme
3,4-Bis(methyloxy)phenol | 3,4-Dimethoxyphenol, 97% | MFCD00008390 | UNII-38B43WCU83 | 3 pound not4-dimethoxyphenol | TS-02054 | AKOS005146109 | 3,4-DIMETHOXYPHENOL | 3,4-dimethoxy-phenol | SY017636 | 38B43WCU83 | Q-101910 | AE-508/42302277 | FT-0614348 |
Spezifikationen & Reinheit
≥97%
Storage
Room temperature
Verschickt in
Normal
Aktionsart
INHIBITOR
Reinheit
≥97%
Namen und Kennungen
Pubchem Sid488182219
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182219
Kanonisches LächelnCOC1=C(C=C(C=C1)O)OC
IUPAC Name3,4-dimethoxyphenol
InChIKeySMFFZOQLHYIRDA-UHFFFAOYSA-N
INCHI1S/C8H10O3/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5,9H,1-2H3
Isomere SMILES COC1=C(C=C(C=C1)O)OC
WGK Deutschland 3
Molekulargewicht 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=

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
SuperclassBenzenoids
KlassePhenols
SubclassMethoxyphenols
Intermediate Tree Nodes Not available
Direct ParentMethoxyphenols
Alternative Parents Dimethoxybenzenes  4-alkoxyphenols  Phenoxy compounds  Anisoles  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  Hydrocarbon derivatives  
Molecular FrameworkAromatic 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
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

12 results found

Lot NumberCertificate TypeDatumArtikel
C2323880Certificate of AnalysisSep 08, 2026 D107922
C2323915Certificate of AnalysisSep 08, 2026 D107922
C2323941Certificate of AnalysisSep 08, 2026 D107922
C2323944Certificate of AnalysisSep 08, 2026 D107922
C2323959Certificate of AnalysisSep 08, 2026 D107922
C2323961Certificate of AnalysisSep 08, 2026 D107922
C2323962Certificate of AnalysisSep 08, 2026 D107922
C2323963Certificate of AnalysisSep 08, 2026 D107922
H2529087Certificate of AnalysisSep 04, 2025 D107922
B2521187Certificate of AnalysisJun 18, 2024 D107922
H1815038Certificate of AnalysisJan 05, 2024 D107922
C2123097Certificate of AnalysisDec 15, 2022 D107922

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Chemische und physikalische Eigenschaften
LöslichkeitSoluble in water.
EmpfindlichkeitLight Sensitive
Siedepunkt (°C)167°C/14mmHg
Schmelzpunkt (°C)80°C
Molekulargewicht154.160 g/mol
XLogP31.700
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass154.063 Da
Monoisotopic Mass154.063 Da
Topological Polar Surface Area38.700 Ų
Heavy Atom Count11
Formal Charge0
Complexity116.000
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
Referenzen
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]
Lösungsrechner
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