Name: 3-Methoxycatechol - ≥98%(GC) , CAS No.934-00-9
SKU: M157868
Availability: InStock

3-Methoxycatechol - ≥98%(GC) , CAS No.934-00-9

CAS: 934-00-9 Cat. No.: M157868 Summenformel: C₇H₈O₃ Molekulargewicht: 140.14 Beilstein Registry Number: 1909170 EG-Nummer: 213-276-4

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3-Methoxycatechol - ≥98%(GC) CAS No(934-00-9) by Aladdin Scientific

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GRADE & PURITY ≥98%(GC)

Synonyms

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Citations of This Product Referenzen Lösungsrechner Bewertungen

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Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme

Spezifikationen & Reinheit

≥98%(GC)

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%(GC)

Namen und Kennungen

Pubchem Sid	504752472
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752472
Kanonisches Lächeln	COC1=CC=CC(=C1O)O
IUPAC Name	3-methoxybenzene-1,2-diol
InChIKey	LPYUENQFPVNPHY-UHFFFAOYSA-N
INCHI	1S/C7H8O3/c1-10-6-4-2-3-5(8)7(6)9/h2-4,8-9H,1H3
Isomere SMILES	COC1=CC=CC(=C1O)O
WGK Deutschland	3
RTECS	CZ9002750
Molekulargewicht	140.14
Beilstein	1909170
Reaxy-Rn	1909165
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1909165&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.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Klasse Phenols
    - Subclass Methoxyphenols

Kingdom	Organic compounds
Superclass	Benzenoids
Klasse	Phenols
Subclass	Methoxyphenols
Intermediate Tree Nodes	Not available
Direct Parent	Methoxyphenols
Alternative Parents	Phenoxy compounds Methoxybenzenes Catechols Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Methoxyphenol - Phenoxy compound - Methoxybenzene - Phenol ether - Catechol - 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
Beschreibung	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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

Zugehörige Ziele (menschlich)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX12 Tchem Arachidonate 12-lipoxygenase (3262 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

POLK Tbio DNA polymerase kappa (8653 Activities)

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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LMNA Tbio Prelamin-A/C (36751 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Zugehörige Ziele (nicht menschlich)

Mapk1 MAP kinase ERK2 (650 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mapt Microtubule-associated protein tau (6 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rorc Nuclear receptor ROR-gamma (89407 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Impa1 Inositol monophosphatase 1 (16203 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

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.

19 results found

Lot Number	Certificate Type	Datum	Artikel
F2124034	Certificate of Analysis	Apr 08, 2025	M157868
F2124033	Certificate of Analysis	Apr 08, 2025	M157868
A2509358	Certificate of Analysis	Apr 03, 2024	M157868
A2509355	Certificate of Analysis	Apr 03, 2024	M157868
D1923052	Certificate of Analysis	Feb 03, 2023	M157868
E2310513	Certificate of Analysis	Dec 01, 2022	M157868
H2631185	Certificate of Analysis	Dec 01, 2022	M157868
E2310798	Certificate of Analysis	Dec 01, 2022	M157868
E2310579	Certificate of Analysis	Dec 01, 2022	M157868
E2310578	Certificate of Analysis	Dec 01, 2022	M157868
E2310574	Certificate of Analysis	Dec 01, 2022	M157868
E2310573	Certificate of Analysis	Dec 01, 2022	M157868
E2310506	Certificate of Analysis	Dec 01, 2022	M157868
D2610115	Certificate of Analysis	Dec 01, 2022	M157868
B2221118	Certificate of Analysis	Jan 14, 2022	M157868
B2219270	Certificate of Analysis	Jan 14, 2022	M157868
B2219264	Certificate of Analysis	Jan 14, 2022	M157868
B2219260	Certificate of Analysis	Jan 14, 2022	M157868
I2502072	Certificate of Analysis	Jan 14, 2022	M157868

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Chemische und physikalische Eigenschaften

Löslichkeit	souble in Methanol
Empfindlichkeit	Air Sensitive,Heat Sensitive
Flammpunkt (°F)	235.4 °F
Flammpunkt (°C)	>110 ℃
Siedepunkt (°C)	164°C
Schmelzpunkt (°C)	38-44℃
Molekulargewicht	140.140 g/mol
XLogP3	0.800
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	140.047 Da
Monoisotopic Mass	140.047 Da
Topological Polar Surface Area	49.700 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	105.000
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

Citations of This Product

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Referenzen

1. Ran Wang, Chong Li, Jianxiang Wu, Wei Du, Tao Jiang, Yizhou Yang, Xuejing Yang, Ming Gong. (2023) Coordination-Promoted Bio-Catechol Electro-Reforming toward Sustainable Polymer Production. Journal of the American Chemical Society, [PMID:37503928] [10.1021/jacs.3c05120]
2. Dongpo He, Jingyu Xu, Yanzhu Guo, Mengtian Yu, Qingyu Wang, Jinghui Zhou, Xing Wang. (2022) RuNi nanoparticles embedded in N-doped carbon nanofibers as a bimetallic catalyst for the hydrogenolysis of peanut shell lignin. FUEL PROCESSING TECHNOLOGY, [PMID:] [10.1016/j.fuproc.2022.107519]

Lösungsrechner

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Bewertungen

📚 Citations by Application

Organic synthesis — reaction medium2

Cross-coupling reactions1

Polymer synthesis & polymerization1

Electrochemistry & battery electrolyte1

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