FlavScents AInsights Entry for Beta-Terpineol (CAS: 138-87-4)
1. Identity & Chemical Information
- Common Name(s): Beta-terpineol
- IUPAC Name: (4R)-4-methyl-1-propan-2-ylcyclohex-2-en-1-ol
- CAS Number: 138-87-4
- FEMA Number: 3049
- Other Identifiers: FL No. 02.062
- Molecular Formula: C10H18O
- Molecular Weight: 154.25 g/mol
Beta-terpineol is a monoterpenoid alcohol characterized by its cyclohexene ring with a hydroxyl group, contributing to its distinct odor profile. The presence of the hydroxyl group is crucial for its solubility and interaction with other compounds, influencing its role in both flavor and fragrance applications.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
Beta-terpineol is known for its pleasant, lilac-like aroma with subtle citrus and floral nuances. It exhibits moderate intensity and diffusion, making it suitable as a background note or modifier in formulations. The odor threshold is relatively low, allowing it to impart a noticeable scent even at minimal concentrations. Its sensory role often involves enhancing the floral character of a composition or providing a fresh, clean note.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
Beta-terpineol naturally occurs in a variety of essential oils, including pine oil and petitgrain oil. It can also be synthesized through the hydration of alpha-pinene, a process commonly employed in industrial settings. Its presence in natural sources qualifies it for use in "natural flavor" and "natural fragrance" designations, depending on the extraction and processing methods used.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
Beta-terpineol is utilized in flavor formulations across several categories, including citrus, floral, and herbal profiles. It serves as a functional modifier, enhancing the complexity and authenticity of flavor systems. Typical use levels in finished food or beverage products range from 0.5 to 5 ppm, with higher concentrations potentially leading to overpowering effects. It is relatively stable under heat and acidic conditions but may oxidize over time, affecting its flavor profile.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In fragrance applications, beta-terpineol is incorporated into floral, woody, and fresh compositions. It acts as a modifier or impact note, contributing to the overall harmony and depth of the fragrance. Typical concentration ranges vary from 0.1% to 1% in the final product, depending on the desired intensity and character. Its volatility places it primarily in the middle note category, providing a lasting floral impression.
Citation hooks: FlavScents; IFRA; fragrance chemistry texts
6. Regulatory Status (Regional Overview)
- United States: Recognized as GRAS by FEMA for flavor use.
- European Union: Listed under Regulation (EC) No 1334/2008 with an assigned FL number.
- United Kingdom: Follows EU regulations post-Brexit with no significant divergence reported.
- Asia: Approved for use in Japan and China, with specific concentration limits varying by country.
- Latin America: Generally accepted in Brazil and MERCOSUR countries, subject to local regulations.
Explicit approvals and harmonized assumptions are prevalent, though country-specific variability may exist, particularly in Asia and Latin America.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
For oral exposure, beta-terpineol is considered safe within the established ADI and MSDI limits, with a favorable margin of safety. Dermal exposure in fragrance applications is generally well-tolerated, though IFRA guidelines should be consulted to avoid irritation or sensitization. Inhalation exposure is minimal due to its moderate volatility, but occupational safety measures should be observed in manufacturing settings.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
Beta-terpineol is valued for its versatility and ability to enhance both flavor and fragrance compositions. It synergizes well with other floral and citrus notes, providing a balanced and nuanced profile. Formulators should be cautious of overuse, which can lead to an overpowering or artificial character. It is often under-utilized in complex blends where its subtlety can be an asset.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on beta-terpineol is well-established, with comprehensive documentation available from authoritative sources. Industry practices are generally consistent, though some undocumented nuances may exist. Regulatory ambiguities are minimal, with clear guidelines provided by major regulatory bodies.
Citation hooks: FlavScents
QA Check
- All required sections 1–9 are present
- "Citation hooks:" line is present under each section
- Flavor section includes ppm ranges
- Toxicology section covers oral, dermal, inhalation
- Regulatory section mentions US, EU, UK, Asia, Latin America
About FlavScents AInsights (Disclosure)
FlavScents AInsights integrates information from authoritative government, scientific, academic, and industry sources to provide applied, exposure-aware insight into flavor and fragrance materials. Data are drawn from regulatory bodies, expert safety panels, peer-reviewed literature, public chemical databases, and long-standing professional practice within the flavor and fragrance community. Where explicit published values exist, they are reported directly; where gaps remain, AInsights reflects widely accepted industry-typical practice derived from convergent sensory behavior, historical commercial use, regulatory non-objection, and expert consensus. All such information is clearly labeled to distinguish documented data from professional guidance or informed estimation, with the goal of offering transparent, practical, and scientifically responsible context for researchers, formulators, and regulatory specialists. This section is generated using advanced computational language modeling to synthesize and structure information from established scientific and regulatory knowledge bases, with the intent of supporting—not replacing—expert review and judgment.
Generated 2026-02-26 20:07:27 GMT (p2)