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3-Ethylphenol

Also known as Phenol, 3-ethyl-, Phenol, m-ethyl-, meta-Ethylphenol, 1-Ethyl-3-hydroxybenzene

3-Ethylphenol is an aromatic phenol containing an ethyl substituent at the meta position. It is supplied for professional chemical synthesis and formulation research.

Aromatic Organic Chemicals Alkylphenols
C₈H₁₀O
C₈H₁₀O

Product identity

CAS number
620-17-7
Molecular formula
C8H10O
Molecular weight
122.16 g/mol
Category
Aromatic Organic Chemicals
Subcategory
Alkylphenols
Common aliases
Phenol, 3-ethyl-, Phenol, m-ethyl-, meta-Ethylphenol

Product overview

What is 3-Ethylphenol?

3-Ethylphenol is an aromatic organic compound belonging to the alkylphenol family. Its canonical name is 3-Ethylphenol, with the systematic name 3-ethylphenol. The compound is also known as meta-ethylphenol, phenol, 3-ethyl-, phenol, m-ethyl-, 1-ethyl-3-hydroxybenzene and benzene, 1-ethyl-3-hydroxy-. Its CAS number is 620-17-7, molecular formula is C8H10O, and molecular weight is 122.16.

The molecule combines a phenolic hydroxyl group with an ethyl substituent on a benzene ring, giving it the positional identity associated with the meta isomer. As an aromatic hydroxyl compound, it can participate in hydrogen bonding and acid-base chemistry characteristic of phenols, while the hydrocarbon substituent influences hydrophobicity and physical behaviour. Actual appearance, odour, phase behaviour and handling characteristics should be confirmed for the selected material.

3-Ethylphenol is principally encountered in laboratory investigation, analytical work and organic synthesis, where its defined substitution pattern can support comparative studies or serve as a starting material for further transformations. Phenolic compounds with alkyl substitution may also be examined in materials, fragrance-related or process-development research, but a particular application should not be inferred solely from the chemical name. End-use acceptance depends on technical evaluation.

Selection should begin with identity confirmation, intended reaction or analytical method, and compatibility with the process environment. Buyers should consider the required documentation, impurity profile, storage conditions, exposure controls and regional obligations relevant to their operation. The stated formula and molecular weight support identification, but they do not establish purity, physical specifications or regulatory status. Suitability of any particular grade requires application-specific assessment before use. For commercial selection, the compound name should be considered separately from the specification and supplied form required for the intended process.

Technical profile

Product properties

Review the product identity and general physical profile before specifying the grade required for your operation.

Category
Aromatic Organic Chemicals
Subcategory
Alkylphenols
IUPAC name
3-ethylphenol
Molecular formula
C8H10O
Molecular weight
122.16 g/mol

Uses and markets

Applications and industries

The correct product specification depends on the intended process, grade requirements and operating conditions.

Detailed product information

Detailed 3-Ethylphenol product information

Identity and molecular structure

3-Ethylphenol is a substituted phenol with an ethyl group positioned meta to the hydroxyl group on the aromatic ring. This arrangement distinguishes it from other ethylphenol isomers and is important when comparing analytical data, reaction pathways or material selection. The compound is identified by CAS 620-17-7 and has the molecular formula C8H10O, corresponding to a molecular weight of 122.16.

For laboratories and manufacturing teams, positional isomer control can matter because closely related aromatic compounds may show different reactivity, chromatographic behaviour and downstream suitability. The listed aliases can assist catalogue searches and document cross-referencing, while the canonical identity should remain the primary basis for specification review and technical communication.

Chemical behaviour and technical evaluation

The phenolic hydroxyl group gives 3-Ethylphenol a characteristic site for hydrogen bonding and acid-base reactions. Its aromatic ring and ethyl substituent contribute to the behaviour expected of an alkyl-substituted phenol. Reaction outcomes depend on catalysts, solvents, temperature, concentration and other process variables, so general structural information should not be treated as a guaranteed performance specification.

Before incorporating this compound into a method or synthesis, users should review compatibility with contact materials, reaction partners and process controls. Analytical identification may involve comparison with suitable reference data and an appropriate method. Physical observations such as colour, odour or state can vary with conditions and should be confirmed from the selected material’s documentation rather than assumed from the name alone.

Research and synthesis context

3-Ethylphenol can be relevant to exploratory organic chemistry because its ring substitution pattern provides a defined platform for studying electrophilic substitution, functional-group transformations and derivative preparation. It may also support analytical comparisons among alkylphenols. These are potential research contexts, not universal claims of suitability, and each proposed route should be assessed for selectivity, yield, work-up requirements and product characterization.

In chemical development, the compound may be considered when a meta-ethyl-substituted phenolic structure is needed in a target intermediate or comparative experiment. The appropriate material depends on the intended scale, reaction sensitivity, impurity tolerance and documentation requirements. A small-scale compatibility study and analytical confirmation are prudent before wider process adoption or incorporation into a more complex formulation.

Selection, storage and handling considerations

Professional selection should address the intended use, required identity evidence, impurity expectations and applicable workplace controls. Users should consult current supplier documentation for storage guidance, handling precautions and material-specific information. Because phenolic compounds may require controlled exposure practices, operations should use suitable engineering controls, personal protective equipment and procedures determined by a competent safety professional.

Storage and transfer practices should be based on the selected material’s safety information, container compatibility and local requirements. Avoid relying on molecular formula or molecular weight to predict all handling needs. Teams should also consider segregation from incompatible reagents, spill response planning, labelling and waste management before introducing 3-Ethylphenol into routine laboratory or production activities.

Frequently asked questions

Questions about 3-Ethylphenol

What distinguishes 3-Ethylphenol from other ethylphenol isomers?

3-Ethylphenol has an ethyl group and a hydroxyl group arranged in the meta, or 1,3-, relationship on the benzene ring. Other ethylphenol isomers place those substituents differently, which can alter steric effects, electronic behaviour, chromatographic retention and reaction outcomes. The distinction is therefore structural rather than merely a naming preference. When an isomer-specific compound is required, users should compare the canonical name, CAS number, formula, analytical data and supporting documentation. A similar formula does not establish interchangeability, particularly in synthesis, method development or quality-control work where positional identity can affect the result.

How does the phenolic group influence its chemistry?

The hydroxyl group is the principal functional feature governing much of 3-Ethylphenol’s chemistry. It can participate in hydrogen bonding and can undergo acid-base reactions characteristic of phenols. The oxygen also provides a site that may be modified or involved in derivative formation, depending on the reagents and conditions. The aromatic ring supports other transformations, while the ethyl substituent influences steric and electronic surroundings. Actual reaction behaviour depends on solvent, temperature, catalysts, concentration and competing functional groups. These variables should be assessed experimentally or through an appropriate validated development approach rather than inferred from structure alone.

What types of laboratory work may involve 3-Ethylphenol?

Potential laboratory contexts include analytical characterization, comparative studies of substituted phenols, organic synthesis and research into aromatic reactivity. It may serve as a defined test material, an intermediate candidate or a structural example in method-development work. The appropriate role depends on the project’s objective, required purity, analytical method and reaction design. Users should establish identity and material suitability before beginning work, particularly when closely related isomers could interfere with measurements. Research use also requires suitable laboratory controls, waste procedures and documentation aligned with the local institution’s rules and the selected material’s safety information.

Can 3-Ethylphenol be used directly in a finished formulation?

Direct use in a finished formulation should not be assumed from the compound’s identity alone. Formulation suitability depends on the intended product, concentration, impurities, stability, compatibility with other ingredients, exposure scenario and applicable legal requirements. A compound that is useful as a laboratory intermediate may not be appropriate for consumer, food, cosmetic or other regulated applications. Development teams should conduct application-specific compatibility and stability studies, review relevant safety information and obtain any required approvals before use. The selected material’s documentation should define the information needed for a responsible formulation decision.

What factors can affect reactions involving 3-Ethylphenol?

Reaction behaviour can be influenced by the chosen solvent, reagent strength, catalyst, temperature, concentration, mixing, reaction time and atmosphere. The phenolic hydroxyl group may participate in proton-transfer or derivatization chemistry, while the aromatic ring can respond to electrophilic or other transformations depending on the system. Water content and trace impurities may also affect sensitive reactions or analytical results. Because several pathways may compete, users should define the desired transformation, review compatibility, monitor progress with an appropriate analytical method and confirm the product identity. Small-scale evaluation is advisable before process expansion.

What should laboratories consider when handling this compound?

Laboratories should review the current safety documentation for the selected material and establish controls appropriate to the task, quantity and exposure potential. Good practice may include controlled transfer, suitable ventilation, compatible containers, protective equipment, clear labelling and planned spill and waste procedures. Contact with the material should be minimized, and personnel should be trained in the relevant operating steps. Storage conditions and segregation should follow documented guidance rather than assumptions based only on the formula. Local occupational, environmental and waste requirements also apply, so institutional procedures should be consulted before routine handling or disposal.

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