FlavScents AInsights Entry for 5-Ethyl Furfural (CAS: 23074-10-4)
1. Identity & Chemical Information
- Common Name(s): 5-Ethyl furfural
- IUPAC Name: 5-Ethyl-2-furaldehyde
- CAS Number: 23074-10-4
- FEMA Number: Not available
- Other Identifiers: Not available
- Molecular Formula: C7H8O2
- Molecular Weight: 124.14 g/mol
5-Ethyl furfural is a furan derivative characterized by an aldehyde group and an ethyl substituent at the 5-position. The presence of the furan ring contributes to its distinctive odor profile, which is often associated with nutty and caramel-like notes. The aldehyde group plays a crucial role in its reactivity and sensory characteristics.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
5-Ethyl furfural is known for its warm, nutty, and caramel-like aroma, which can be described as sweet and slightly woody. It is often used as an impact note in flavor formulations to impart a roasted or baked character. The intensity of its odor is moderate, making it suitable for both background and foreground applications in flavor systems. Specific taste and odor thresholds are not well-documented, but it is typically used in low concentrations due to its potent sensory impact.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
5-Ethyl furfural is not commonly found in nature but can be formed through the Maillard reaction, a chemical reaction between amino acids and reducing sugars that occurs during the cooking and roasting of foods. This reaction is responsible for the development of complex flavors and aromas in baked goods, coffee, and roasted nuts. Its formation through such pathways makes it relevant for "natural flavor" designations when derived from natural processes.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
5-Ethyl furfural is primarily used in flavor formulations to enhance nutty, caramel, and roasted profiles. It is commonly found in flavor categories such as bakery, confectionery, and coffee. Its functional role in flavor systems is as an impact note, providing depth and complexity. Typical use levels in finished food or beverage products range from 0.1 to 5 ppm, with higher concentrations potentially leading to overpowering effects. It is relatively stable under typical processing conditions but may degrade under extreme heat or acidic environments.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In the fragrance industry, 5-ethyl furfural is used to impart warm, sweet, and nutty notes. It is often incorporated into fragrance families such as gourmand and oriental. Its role is typically as a trace realism enhancer or modifier, contributing to the overall complexity of the fragrance. Concentration ranges in fragrance formulations are generally low, often below 0.1%, due to its potent aroma. It contributes primarily to the middle notes of a fragrance composition.
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 guidelines.
- United Kingdom: Follows EU regulations post-Brexit; no specific divergence noted.
- Asia: Limited specific data; general compliance with local flavoring regulations is advised.
- Latin America: No specific data available; adherence to regional flavoring standards 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; general safety practices for flavor compounds should be followed.
- Dermal Exposure: Limited data on irritation or sensitization; IFRA guidelines should be consulted for fragrance use.
- Inhalation Exposure: Volatility suggests potential for inhalation exposure; occupational safety measures should be considered.
Risk profiles may differ between food and fragrance applications, with fragrance use requiring careful consideration of dermal and inhalation exposure.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
5-Ethyl furfural is valued for its ability to impart rich, roasted, and nutty notes, enhancing the sensory profile of both flavors and fragrances. It synergizes well with other caramel and nutty compounds, but formulators should be cautious of its potency to avoid overpowering the final product. It is often under-used in formulations seeking to replicate natural roasting processes.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on 5-ethyl furfural is well-established in terms of its sensory characteristics and formation pathways. However, specific regulatory and toxicological data are limited, necessitating reliance on general industry practices and safety guidelines. Known data gaps include detailed toxicological profiles and comprehensive regulatory listings.
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 2026-01-20 17:59:37 GMT (p2)