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99% Purity 3-Butoxyphenol CAS 18979-72-1

99% Purity 3-Butoxyphenol CAS 18979-72-1

3-Butoxyphenol​ CAS 18979-72-1 is a synthetic aromatic ether and a monoalkyl ether derivative of resorcinol​ (1,3-dihydroxybenzene). Its structure consists of a phenol ring with a hydroxyl group (-OH) and a butoxy group (-O-CH₂-CH₂-CH₂-CH₃) both attached in a meta​ relationship to each other (positions 1 and 3).3-Butoxyphenol is a bifunctional meta-substituted phenolic ether​ that uniquely combines the antioxidant and reactive properties of a phenol​ with the solubilizing power and stability of an alkyl ether. This makes it an exceptional synergistic stabilizer and versatile chemical building block​ for performance-critical formulations.

 

  • Name :

    3-Butoxyphenol
  • CAS No. :

    18979-72-1
  • MF :

    C₁₀H₁₄O₂
  • MW :

    166.22
  • Purity :

    99%
  • Appearance :

    Typically a clear, colorless to pale yellow viscous liquid.
  • Storage Condition :

    Store in a cool, dry, well-ventilated area​ in tightly sealed, corrosion-resistant containers.

Chemical Properties

IUPAC Name:​ 3-Butoxyphenol

Other Common Names:​ Resorcinol monobutyl ether; 1-Hydroxy-3-butoxybenzene

Chemical Formula:​ C₁₀H₁₄O₂

Molecular Weight:​ 166.22 g/mol

Structure:​ HO–C₆H₄–O–C₄H₉ (meta substitution)

Appearance:​ Typically a clear, colorless to pale yellow viscous liquid.

This compound combines the reactivity of a phenolic hydroxyl group with the hydrophobicity and solvent properties of a butyl ether chain, making it a versatile bifunctional intermediate.

Melting Point:​ < 25 °C (Often a liquid at room temperature)

Boiling Point:​ ~ 245-250 °C (at atmospheric pressure)

Density:​ Approximately 1.02 - 1.04 g/cm³

Solubility:​ Soluble in most organic solvents (ethanol, ether, acetone, chloroform, benzene). Very slightly soluble in water due to the hydrophobic butoxy chain.

Acidity:​ The phenolic -OH is weakly acidic (pKa ~9.5-10.5), but less acidic than resorcinol itself due to the electron-donating effect of the alkoxy group.

Reactivity:

    Phenol-like:​ Can undergo reactions typical of phenols, such as esterification, etherification (of the -OH), and electrophilic aromatic substitution (directed by the powerful activating -OH group to positions ortho and para to it, primarily positions 2, 4, and 6).

    Ether-like:​ The butoxy ether linkage is generally stable but can be cleaved under strong acidic conditions (e.g., HI, HBr).

 

Biological Activities

Antioxidant Activity:​ The phenolic structure provides inherent radical-scavenging potential, making it a mild antioxidant. It can inhibit autoxidation in susceptible systems.

Antimicrobial Activity:​ Exhibits mild to moderate bacteriostatic and fungistatic properties, common to many phenolic compounds. Its efficacy is enhanced by the lipid-soluble butoxy group, which aids in disrupting microbial membranes.

Skin-related Effects:​ As a derivative of resorcinol—a known keratolytic and antiseptic agent—it may share some mild, localized topical activity. However, its etherification significantly modifies its potency and absorption compared to resorcinol.

Toxicity Profile:​ Generally considered low to moderate toxicity. It is expected to be irritating to eyes, skin, and mucous membranes. Like many phenols, it may be harmful if swallowed or absorbed through the skin in significant quantities. Comprehensive toxicological data is more limited than for commodity chemicals.

 

Biosynthesis

Natural Occurrence:​ Not known as a significant natural product.

Industrial Synthesis:​ Produced almost exclusively via chemical synthesis.

1.Williamson Ether Synthesis:​ The primary industrial route involves the reaction of resorcinol​ with butyl halide​ (e.g., n-butyl chloride or bromide) in the presence of a base (e.g., K₂CO₃, NaOH). This reaction can yield a mixture of monoalkylated (3-butoxy and 4-butoxy) and dialkylated products, which are separated via distillation and purification.

2.Alternative Route:​ Alkylation of resorcinol with butanol in the presence of an acid catalyst, though this method can be less selective.

 

Applications

  • #
    Chemical Intermediate
    Its primary use is as a building block for synthesizing more complex molecules, particularly in the fine chemicals sector.
    UV Absorbers & Stabilizers:​ A key precursor in the synthesis of benzotriazole-type and triazine-type UV absorbers​ used in plastics, coatings, and cosmetics to protect against photodegradation.
    Pharmaceutical & Agrochemical Synthesis:​ The meta-substituted phenolic ether moiety is a valuable scaffold for constructing active ingredients where specific hydrogen bonding and lipophilicity are required.
  • #
    Performance Additive
    Cosmetics & Personal Care:​ Used in very low concentrations as a stabilizer and antioxidant​ in emulsion-based products like creams and sunscreens. It can also function as a solubilizer​ for other ingredients.
    Industrial Fluids:​ Acts as a mild antioxidant and biostat in functional fluids such as coolants, metalworking fluids, and lubricants.
     
  • #
    Research & Development
    Used in organic synthesis laboratories to study reaction pathways of asymmetrically substituted phenols and to develop new polymeric materials.
     

 

Key Advantages & Benefits

1. Dual-Functionality: Reactive Phenol + Solubilizing Ether

Benefit:​ Provides inherent radical-scavenging antioxidant activity​ from its phenolic -OH group, while the butoxy chain enhances solubility in organic matrices​ and acts as a mild hydrophobicity modifier.

Application Scenario:​ In high-stability sunscreen formulations (SPF 50+ lotions), it protects organic UV filters (like avobenzone) from oxidative degradation, while its ether structure ensures it remains fully soluble in the oil phase, preventing crystallization or phase separation. This extends the product's shelf life and maintains protective efficacy.

2. Enhanced Stability Over Plain Phenols

Benefit:​ The ether linkage significantly reduces susceptibility to oxidation and color formation​ (yellowing) compared to parent compounds like resorcinol, ensuring long-term clarity and performance in finished products.

Application Scenario:​ As a stabilizer in clear polyurethane coatings or adhesives, it prevents resin yellowing caused by heat and UV exposure without introducing discoloration of its own, maintaining aesthetic quality.

3. Precise Synthon for Advanced UV Absorbers

Benefit:​ The meta-positioned -OH group is highly reactive and perfectly oriented for cyclization reactions, making it a key precursor for high-performance benzotriazole and triazine-class UV absorbers.

Application Scenario:​ In the synthesis of broad-spectrum light stabilizers for automotive coatings and engineering plastics, it provides the specific molecular backbone that maximizes UV absorption efficiency and thermal stability in the final additive.

4. Favorable Toxicological & Handling Profile

Benefit:​ Offers a safer, less irritating alternative to resorcinol​ and many volatile phenolic solvents. It has lower dermal absorption and reduced volatility (higher boiling point), improving workplace safety.

Application Scenario:​ In hair dye and colorant formulations​ where phenolic compounds are used as couplers or stabilizers, 3-butoxyphenol can provide antioxidant benefits with a significantly reduced risk of skin sensitization, contributing to a milder product profile.

 

3-Butoxyphenol (CAS 18979-72-1)​ is a high-value, multifunctional specialty chemical​ whose strength lies in its hybrid structure. It is not a commodity antioxidant​ but a strategic tool​ for solving specific challenges. It excels where solubility, stability, and phenolic functionality must converge, such as in stabilizing high-performance sun care products, synthesizing advanced light stabilizers, or boosting antioxidant systems in demanding industrial applications. For formulators and chemists, it provides a superior balance of performance, safety, and versatility​ compared to more reactive phenols or inert ethers alone.

 

FAQs 

Q1: What is the main value proposition of 3-Butoxyphenol for formulators?

A:​ It offers a unique dual-functionality: the reactive site of a phenol (for antioxidant activity or further synthesis) combined with the solubilizing and hydrophobicity-modifying power of a butyl ether. This makes it an effective bridging molecule​ to improve compatibility between polar and non-polar phases in formulations and a precise synthon​ for creating meta-substituted aromatic target molecules.

Q2: How does it compare to Resorcinol itself?

A:​ Key Advantages over Resorcinol:

Stability:​ Much less prone to oxidation and discoloration.

Reduced Skin Penetration & Irritation:​ The etherification dramatically lowers its dermal absorption and associated skin sensitization potential.

Lipophilicity:​ The butoxy group grants significant oil solubility, making it easier to incorporate into fat-based formulations.

Disadvantage:​ Lacks the strong keratolytic and antiseptic potency of resorcinol. They are not direct substitutes but tools for different purposes.

Q3: What are the critical handling and storage requirements?

A:​ Store in a cool, dry, well-ventilated area​ in tightly sealed, corrosion-resistant containers (stainless steel or lined drums). Protect from light, heat, and moisture​ to prevent degradation. It has a flash point > 100°C, but as an organic liquid, it should be kept away from ignition sources. Shelf life is typically 24 months​ under proper conditions.

Q4: Can it be used as a standalone preservative in cosmetic products?

A: No, it is not a broad-spectrum preservative.​ While it exhibits mild antimicrobial activity, it is not sufficient to meet preservation efficacy testing standards​ (e.g., USP <51>, EP, or CTFA) alone. It should be used as a supplement or co-preservative​ within a robust, approved preservative system, primarily contributing antioxidant functionality.

Q5: Is it compatible with common formulation ingredients?

A:​ Yes, it has excellent compatibility​ with a wide range of:

Oils & Esters:​ (e.g., Caprylic/capric triglyceride, isopropyl myristate).

Emulsifiers:​ (e.g., Polysorbates, cetearyl alcohol).

Common Organic Solvents.

Use with Caution:​ With strong oxidizing agents and strong bases, which may cause decomposition or reaction. Always conduct compatibility tests in the final formulation matrix.

Q6: What is its regulatory status for use in cosmetics or consumer products?

A:​ It is not specifically listed on major positive lists (like the EU Annexes), but it is also not banned. Its use falls under the general safety provisions of regulations (like the EU Cosmetics Regulation 1223/2009). Safety assessments​ by a qualified toxicologist are required for final product notification. It is not CMR (Carcinogenic, Mutagenic, or Reprotoxic) classified under current GHS.

Q7: Where can we source it, and what are typical specifications?

A:​ It is a specialty chemical​ available from fine chemical suppliers and manufacturers in Asia, Europe, and North America. Typical specifications include:

Purity:​ ≥ 98.0% (GC)

Appearance:​ Colorless to light yellow clear liquid

Water Content:​ ≤ 0.5% (Karl Fischer)

Resorcinol Content:​ ≤ 0.5% (as a key impurity to control)

 

 

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