Name: Isoeugenol - analytical standard, for environmental analysis , CAS No.97-54-1
SKU: I109576
Availability: InStock

Isoeugenol - analytical standard, for environmental analysis , CAS No.97-54-1

CAS: 97-54-1 Cat. No.: I109576 Summenformel: C₁₀H₁₂O₂ Molekulargewicht: 164.20 Beilstein Registry Number: 1909602 EG-Nummer: 202-590-7

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GRADE & PURITY Analytical standard ? for Environmental analysis ?

Synonyms

Storage

Room temperature

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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 FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Why this grade

analytical standard, for environmental analysis Analytischer Standard,für die Umweltanalyse for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature 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.

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Literature proof

Cited in 21 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme

Spezifikationen & Reinheit

analytical standard, for environmental analysis

Storage

Room temperature

Verschickt in

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Note

Analytischer Standard, für die Umweltanalyse

Namen und Kennungen

Pubchem Sid

528771697

Kanonisches Lächeln

CC=CC1=CC(=C(C=C1)O)OC

IUPAC Name

2-methoxy-4-[(E)-prop-1-enyl]phenol

InChIKey

BJIOGJUNALELMI-ONEGZZNKSA-N

INCHI

1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3-7,11H,1-2H3/b4-3+

Isomere SMILES

C/C=C/C1=CC(=C(C=C1)O)OC

WGK Deutschland

RTECS

SL7875000

Molekulargewicht

164.20

Beilstein

1909602

Reaxy-Rn

1909602

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1909602&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	Styrenes Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Methoxyphenol - Phenoxy compound - Methoxybenzene - Styrene - Phenol ether - Anisole - 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	isoeugenol
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)

TYR Tclin Tyrosinase (717 Activities)

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DU-145 (51482 Activities)

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HL-60 (67320 Activities)

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HT-1080 (3966 Activities)

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MCF7 (126967 Activities)

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Raji (5516 Activities)

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U-937 (7138 Activities)

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A549 (127892 Activities)

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HepG2 (196354 Activities)

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KB (17409 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)

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Zugehörige Ziele (nicht menschlich)

Staphylococcus aureus (210822 Activities)

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Aspergillus fumigatus (16427 Activities)

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Plasmodium falciparum (966862 Activities)

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3LL cell line (138 Activities)

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lef Anthrax lethal factor (7585 Activities)

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Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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ddn Putative uncharacterized protein (49 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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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.

2 results found

Lot Number	Certificate Type	Datum	Artikel
D2523023	Certificate of Analysis	Apr 30, 2025	I109576
F2011037	Certificate of Analysis	Jan 17, 2024	I109576

Chemische und physikalische Eigenschaften

Brechungsindex	1.5748
Flammpunkt (°F)	233.6 °F
Flammpunkt (°C)	134℃
Siedepunkt (°C)	266°C
Schmelzpunkt (°C)	13°C
Molekulargewicht	164.200 g/mol
XLogP3	2.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	164.084 Da
Monoisotopic Mass	164.084 Da
Topological Polar Surface Area	29.500 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	154.000
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

FAQs und Artikel

What Are Environmental Analysis Reagents? A Comprehensive Guide from Grade to Selection

Categories: Reagent Specifications, Grading and Purity

Tags:

for environmental analysis

Structure–Property Relationships and Identification of Phenylpropenes: Side-Chain Double-Bond Position, Oxygenated Aromatic-Ring Substitution, and E/Z Configuration

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Phenylpropenes

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Lösungsrechner

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Bewertungen

📚 Citations by Application

Organic synthesis — reaction medium13

Other applications8

Electrochemistry & battery electrolyte2

Polymer synthesis & polymerization1

Extraction & workup solvent9

Chromatography (HPLC / GC / TLC)2

Spectroscopy sample preparation2

Cross-coupling reactions1

Industrial & non-pharma application1

Drug / compound screening1

Cytotoxicity screening1

Crystallization & recrystallization1

View all 21 citations →

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Isoeugenol - analytical standard, for environmental analysis , CAS No.97-54-1

Storage & shipping

Quality documents

Literature proof

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Citations by Application

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