FlavScents AInsights Entry for Duryl Aldehyde (CAS: 5779-72-6)
1. Identity & Chemical Information
- Common Name(s): Duryl Aldehyde
- IUPAC Name: 2,3,5,6-Tetramethylbenzaldehyde
- CAS Number: 5779-72-6
- FEMA Number: Not available
- Other Identifiers: Not available
- Molecular Formula: C11H14O
- Molecular Weight: 162.23 g/mol
Duryl aldehyde is characterized by its aromatic aldehyde functional group, which contributes to its distinctive odor profile. The presence of four methyl groups on the benzene ring enhances its hydrophobic character and influences its volatility and odor intensity.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
Duryl aldehyde is known for its sweet, floral, and slightly woody odor, often described as reminiscent of hawthorn or almond blossoms. It has a moderate intensity and diffusion, making it suitable for use as an impact note in fragrance compositions. The taste and odor thresholds are not clearly reported, but it is typically used in low concentrations due to its potent sensory characteristics.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
Duryl aldehyde is not commonly found in nature and is primarily synthesized for industrial use. It does not have significant natural sources and is not typically associated with natural flavor or fragrance designations. Its formation is generally achieved through chemical synthesis rather than natural biosynthetic pathways.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
Duryl aldehyde is used in flavor formulations to impart a sweet, floral note, often enhancing the complexity of fruit and floral flavors. It is typically used in low concentrations, generally ranging from 0.1 to 5 ppm in finished food products, depending on the desired intensity and application. It is stable under typical food processing conditions but may degrade under extreme heat or acidic conditions.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In fragrance applications, duryl aldehyde is valued for its ability to add a sweet, floral character to compositions. It is used across various fragrance families, including floral, oriental, and woody. Its role can vary from a trace realism enhancer to a prominent impact note. Typical usage levels range from 0.01% to 0.1% in fragrance formulations, contributing primarily to the top and middle notes due to its moderate volatility.
Citation hooks: FlavScents; IFRA; fragrance chemistry texts
6. Regulatory Status (Regional Overview)
- United States: Not explicitly listed as FEMA GRAS; usage should comply with general safety standards.
- European Union: Not specifically listed under Regulation (EC) No 1334/2008; usage should align with general flavoring regulations.
- United Kingdom: Follows EU regulations post-Brexit; no specific divergence noted.
- Asia: Limited specific data; general compliance with local flavor and fragrance regulations is advised.
- Latin America: No specific data; adherence to MERCOSUR and local regulations is recommended.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
- Oral Exposure: Data not found for specific ADI or MSDI values; usage should be guided by general safety assessments and industry practices.
- Dermal Exposure: Limited data on irritation or sensitization; formulators should consider IFRA guidelines for aldehydes.
- Inhalation Exposure: Moderate volatility suggests potential for inhalation exposure; occupational safety measures should be considered in manufacturing settings.
Risk profiles may differ between food and fragrance applications due to differing exposure routes and concentrations.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
Duryl aldehyde is valued for its ability to impart a sweet, floral character, enhancing both flavor and fragrance compositions. It synergizes well with other floral and fruity notes, but care should be taken to avoid overuse, which can lead to an overpowering or artificial scent. It is often under-utilized in complex formulations where subtlety is required.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on duryl aldehyde is well-established in terms of its chemical identity and sensory profile. However, there are gaps in specific regulatory approvals and toxicological data, which necessitate cautious use and adherence to general safety guidelines.
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 2026-08-24 06:00:21 GMT (p2)