3-Methoxyphenol - ≥97% , CAS No.150-19-6

CAS: 150-19-6 Cat. No.: M109432 Formula: C7H8O2 Peso molecolare: 124.14 Beilstein Registry Number: 1209898 Numero EC: 205-754-6
Disponibile su ordine
GRADE & PURITY ≥97%
Synonyms
A809020 | EINECS 205-754-6 | MFCD00002267 | W-108077 | m-Guaiacol | 3-(methyloxy)phenol | CAS-150-19-6 | Resorcinol methyl ether | BDBM36297 | 1-Hydroxy-3-methoxybenzene | SCHEMBL28256 | 3-Methoxyphenol, analytical standard | FT-0616005 | ORISTAR HOA | Ph
Storage
Room temperature,Argon charged
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
5g
M109432-5g
—
3 Disponibile
8,59€
10g
M109432-10g
—
1 Disponibile
9,46€
25g
M109432-25g
—
4 Disponibile

13,80€

20,74€
Salva 6,94 € (33.47%)
100g
M109432-100g
—
3 Disponibile

35,49€

53,71€
Salva 18,22 € (33.93%)
500g
M109432-500g
1 Disponibile
—

163,92€

246,35€
Salva 82,44 € (33.46%)
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature,Argon charged 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.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

It was used in synthesis of:C(4) symmetric calix[4]resorcinarene;2-nitroso-5-methoxyphenol;6-methoxy-2(3H)-benzoxazolone.

Specifications

Sinonimi
A809020 | EINECS 205-754-6 | MFCD00002267 | W-108077 | m-Guaiacol | 3-(methyloxy)phenol | CAS-150-19-6 | Resorcinol methyl ether | BDBM36297 | 1-Hydroxy-3-methoxybenzene | SCHEMBL28256 | 3-Methoxyphenol, analytical standard | FT-0616005 | ORISTAR HOA | Ph
Specifiche e purezza
≥97%
Condizioni di conservazione di stoccaggio
Room temperature,Argon charged
Spedito in
Normal
Purezza
≥97%
Nomi e identificatori
Pubchem Sid488180920
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180920
Sorrisi canoniciCOC1=CC=CC(=C1)O
IUPAC Name3-methoxyphenol
InChIKeyASHGTJPOSUFTGB-UHFFFAOYSA-N
INCHI1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3
Isomeri SMILES COC1=CC=CC(=C1)O
WGK Germania 3
RTECS SL7524000
Numero UN 2810
Peso molecolare 124.14
Beilstein 1209898
Reaxy-Rn 1209898
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209898&ln=

Documentazione

📋 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
ClassePhenols
SubclassMethoxyphenols
Intermediate Tree Nodes Not available
Direct ParentMethoxyphenols
Alternative Parents Phenoxy compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Methoxyphenol - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescrizioneThis 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 phenols - monomethoxybenzene
Struttura 3D
Modello di struttura chimica interattiva





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Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

22 results found

Lot NumberCertificate TypeDataOggetto
D2318271Certificate of AnalysisSep 21, 2026 M109432
E1910109Certificate of AnalysisJul 07, 2026 M109432
E2431076Certificate of AnalysisMar 11, 2026 M109432
J2114393Certificate of AnalysisApr 03, 2025 M109432
J2114392Certificate of AnalysisApr 03, 2025 M109432
G2105068Certificate of AnalysisJan 09, 2025 M109432
F2421040Certificate of AnalysisJun 27, 2024 M109432
F2415022Certificate of AnalysisJun 25, 2024 M109432
G2507030Certificate of AnalysisJun 25, 2024 M109432
G2530025Certificate of AnalysisJun 25, 2024 M109432
D2423278Certificate of AnalysisMar 25, 2024 M109432
D2423279Certificate of AnalysisMar 25, 2024 M109432
I1806025Certificate of AnalysisJan 18, 2024 M109432
J2114394Certificate of AnalysisJul 11, 2023 M109432
J2114395Certificate of AnalysisJul 11, 2023 M109432
K2228313Certificate of AnalysisOct 12, 2022 M109432
K2228314Certificate of AnalysisOct 12, 2022 M109432
K2228315Certificate of AnalysisOct 12, 2022 M109432
K2228316Certificate of AnalysisOct 12, 2022 M109432
K2228317Certificate of AnalysisOct 12, 2022 M109432
K2228318Certificate of AnalysisOct 12, 2022 M109432
L2320023Certificate of AnalysisOct 12, 2022 M109432

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Proprietà chimiche e fisiche
SolubilitàSolubility in water: Slightly soluble
Sensibilitàair sensitive
Indice di rifrazione1.551-1.553
Punto di infiammabilità (°F)233.6 °F
Punto di infiammabilità (°C) 114°C
Punto di ebollizione (°C)244°C
Punto di fusione (°C)-17°C
Peso molecolare124.140 g/mol
XLogP31.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass124.052 Da
Monoisotopic Mass124.052 Da
Topological Polar Surface Area29.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity83.000
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
Riferimenti
1. Haoquan Guo, Xinyu Lu, Yue Yang, Jinhe Wei, Lizhi Wu, Li Tan, Yu Tang, Xiaoli Gu.  (2023)  Harvesting alkyl phenols from lignin monomers via selective hydrodeoxygenation under ambient pressure on Pd/α-MoC catalysts.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2023.113041]
2. 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]
3. Sui-Qin Yang, Zheng-Qian Liu, Yu-Hong Cui, Ming-Kui Wang.  (2022)  Organics abatement and recovery from wastewater by a polymerization-based electrochemically assisted persulfate process: Promotion effect of chloride ion and its mechanism.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:36580777] [10.1016/j.jhazmat.2022.130658]
4. Fei Zhang, Chunzheng Wu, Shuibo Wang, Shiwei Wang, Tong Li, Laixi Zou, Hongbo Yu, Hongfeng Yin.  (2022)  Tailoring the activity and selectivity of Rh/SiO2 for the selective hydrogenation of phenol by CoOx promotion.  Catalysis Science & Technology,  12  (7): (2257-2264).  [PMID:] [10.1039/D1CY02324A]
5. Xiaojiang Li, Leitao Sun, Xin Lv, Jie Qi, Hongsheng Lu, Yuanpeng Wu, Baogang wang.  (2021)  Sustainable separation of petroleum hydrocarbons pollutant using hydrophobic deep eutectic solvents regulated by CO2.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2021.106280]
6. Xiaohao Liu, Wenda Jia, Guangyue Xu, Ying Zhang, Yao Fu.  (2017)  Selective Hydrodeoxygenation of Lignin-Derived Phenols to Cyclohexanols over Co-Based Catalysts.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.7b01047]
7. Yue Zhang, Zhiyong Li, Huiyong Wang, Xiaopeng Xuan, Jianji Wang.  (2016)  Efficient separation of phenolic compounds from model oil by the formation of choline derivative-based deep eutectic solvents.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2016.03.014]
8. Guangfan Han, Jiawei Du, Lizhuang Chen, Lijun Zhao.  (2014)  Synthesis and Characterization of 11-Amino-3-methoxy-8-substituted-12-aryl-8,9-dihydro-7H-chromeno[2,3-b]quinolin-10(12H)-one Derivatives.  JOURNAL OF HETEROCYCLIC CHEMISTRY,  51  (4): (1094-1099).  [PMID:] [10.1002/jhet.2010]
9. Zihang Shen, Zheyu Dong, Jiabao Bai, Daochen Yin, Zhi Sheng, Yijie Cai, Zheng Jia.  (2025)  Protocol for the fabrication and application of a low-water-content polyelectrolyte hydrogel.  STAR Protocols,      [PMID:40127102] [10.1016/j.xpro.2025.103713]
10. Dong-hong Nan, Cheng-bo Zhang, Qi Niu, Shi-yu Feng, Bin Hu, Ji Liu, Kai Li, Qiang Lu.  (2025)  Nitrogen-doped hydrothermal carbon as a catalyst for selective alkoxyphenol production from pine pyrolysis.  BIOMASS & BIOENERGY,      [PMID:] [10.1016/j.biombioe.2025.108180]
11. Qishu Qu, Han Xuan, Kehua Zhang, Yi Ding, Qin Xu.  (2016)  Layer-by-layer assembly of zeolite imidazolate framework-8 as coating material for capillary electrochromatography.  ELECTROPHORESIS,      [PMID:27174427] [10.1002/elps.201600121]
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