FlavScents AInsights Entry for Tetrahydrolinalool (CAS: 78-69-3)
1. Identity & Chemical Information
- Common Name(s): Tetrahydrolinalool
- IUPAC Name: 3,7-dimethyloctan-3-ol
- CAS Number: 78-69-3
- FEMA Number: 3065
- Other Identifiers: FL No. 02.091
- Molecular Formula: C10H22O
- Molecular Weight: 158.28 g/mol
Tetrahydrolinalool is a saturated alcohol derived from linalool, characterized by its lack of double bonds. This structural modification results in a more stable compound with a distinct odor profile. The presence of the hydroxyl group contributes to its solubility in alcohols and its moderate polarity, influencing its behavior in formulations.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
Tetrahydrolinalool is known for its fresh, floral, and slightly woody aroma, often described as reminiscent of lily of the valley. It exhibits moderate intensity and diffusion, making it suitable for both impact and background roles in fragrance compositions. While specific taste thresholds are not well-documented, its odor threshold is relatively low, allowing it to impart noticeable effects even at low concentrations.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
Tetrahydrolinalool is not typically found in nature but is synthesized through the hydrogenation of linalool, a naturally occurring terpene alcohol found in many essential oils, such as lavender and coriander. This synthetic pathway allows for its use in "nature-identical" flavor and fragrance applications, aligning with regulatory definitions of natural flavors when derived from natural precursors.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
Tetrahydrolinalool is utilized in a variety of flavor applications, particularly in floral and citrus profiles. It serves as a modifier and enhancer, providing depth and complexity to flavor systems. Typical use levels in finished products range from 0.5 to 5 ppm, with higher concentrations potentially leading to overpowering effects. Its stability under heat and acidic conditions makes it a versatile component in both beverages and confectionery.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In perfumery, tetrahydrolinalool is valued for its ability to impart a fresh, floral note, fitting well within floral, woody, and citrus fragrance families. It acts as a middle note, contributing to the fragrance's heart with moderate volatility. Typical concentrations range from 0.1% to 1% in finished products, depending on the desired intensity and role within the fragrance composition.
Citation hooks: FlavScents; IFRA; fragrance chemistry texts
6. Regulatory Status (Regional Overview)
- United States: Recognized as GRAS by FEMA for flavor use.
- European Union: Approved under Regulation (EC) No 1334/2008 with FL No. 02.091.
- United Kingdom: Aligns with EU regulations post-Brexit.
- Asia: Generally accepted in Japan and China, though specific regulatory details may vary.
- Latin America: Accepted in Brazil and MERCOSUR countries, with harmonized assumptions across the region.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
Tetrahydrolinalool is considered safe for use in both flavor and fragrance applications, with a favorable safety profile. Oral exposure through flavor use is supported by FEMA GRAS status, with no specific ADI established but considered safe at typical use levels. Dermal exposure in fragrances is generally well-tolerated, with low potential for irritation or sensitization, aligning with IFRA guidelines. Inhalation exposure is minimal due to its moderate volatility, posing low occupational risk.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
Tetrahydrolinalool is prized for its versatility and ability to enhance floral and citrus notes without dominating the composition. It synergizes well with other floral and woody components, providing a smooth transition between top and middle notes. Formulators should be cautious of overuse, which can lead to an overly synthetic character. It is often underutilized in complex fragrance systems where its subtlety can add depth.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on tetrahydrolinalool is well-established, with consistent findings across sensory and regulatory domains. While specific numeric thresholds for taste are not well-documented, industry practices provide reliable guidance. Regulatory frameworks are harmonized across major markets, though formulators should verify compliance with local regulations.
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
- If complex natural material: includes section 5a (not applicable here)
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 2026-06-28 00:25:03 GMT (p2)