FlavScents AInsights Entry for Dimethyl Dihydrocyclopentapyrazine (CAS: 38917-61-2)
1. Identity & Chemical Information
- Common Name(s): Dimethyl dihydrocyclopentapyrazine
- IUPAC Name: 2,3-Dimethyl-5,6-dihydrocyclopenta[b]pyrazine
- CAS Number: 38917-61-2
- FEMA Number: Not available
- Other Identifiers: Not available
- Molecular Formula: C8H12N2
- Molecular Weight: 136.20 g/mol
- Functional Groups and Structure–Odor Relevance: This compound contains a pyrazine ring, which is known for contributing to roasted, nutty, and earthy aromas. The dimethyl substitution enhances its odor intensity and complexity.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
Dimethyl dihydrocyclopentapyrazine is characterized by its potent roasted, nutty, and earthy aroma, often described as reminiscent of roasted nuts or coffee. It has a strong odor intensity and is typically used as an impact note in flavor formulations. The compound's diffusion is moderate, allowing it to blend well with other flavor components without overpowering them. Specific taste and odor thresholds are not clearly reported, but it is known to be effective at low concentrations.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
Dimethyl dihydrocyclopentapyrazine 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 process. This reaction is responsible for the development of complex flavors and aromas in cooked foods, making this compound relevant for "natural flavor" designations when derived from such processes.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
Dimethyl dihydrocyclopentapyrazine is used in various flavor categories, including savory, nutty, and roasted profiles. It serves as an impact note, providing depth and authenticity to flavor systems. Typical use levels in finished food products range from 0.1 to 5 ppm, with higher concentrations used in more robust applications like coffee or roasted nut flavors. The compound is stable under heat and neutral pH conditions but may degrade under highly acidic or oxidative environments.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In fragrances, dimethyl dihydrocyclopentapyrazine is used to impart a warm, nutty, and earthy aroma, fitting well within the gourmand and woody fragrance families. It acts as a modifier, enhancing the realism of the fragrance profile. Typical concentrations range from trace amounts to 0.5% in the final product, depending on the desired intensity. The compound contributes primarily to the 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; assumed safe under general flavoring guidelines.
- United Kingdom: Follows EU regulations post-Brexit with no significant divergence reported.
- Asia: Limited specific data; generally follows international safety standards.
- Latin America: No specific regulations identified; assumed to follow international norms.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
- Oral Exposure: No specific ADI or MSDI values reported; considered safe at typical flavor use levels.
- Dermal Exposure: Limited data on irritation or sensitization; generally considered low risk in fragrance applications.
- Inhalation Exposure: Moderate volatility suggests low occupational risk; standard ventilation practices recommended.
Risk profiles do not significantly differ between food and fragrance applications, assuming adherence to recommended use levels.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
Dimethyl dihydrocyclopentapyrazine is valued for its ability to impart a rich, roasted character to both flavors and fragrances. It synergizes well with other pyrazines and nutty compounds, enhancing complexity. Formulators should be cautious of overuse, as its potent aroma can dominate blends. It is often under-utilized in lighter applications where subtlety is desired.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
Data on dimethyl dihydrocyclopentapyrazine is well-established in terms of sensory characteristics and typical use levels. However, specific regulatory approvals and toxicological data are less documented, relying on industry norms and general safety assessments.
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
- Not a complex natural material; section 5a not applicable
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 2026-05-13 23:41:13 GMT (p2)