FlavScents AInsights Entry for cis-Isopinocamphone (CAS: 15358-88-0)
1. Identity & Chemical Information
- Common Name(s): cis-Isopinocamphone
- IUPAC Name: (1R,5R)-2,2,3-Trimethylbicyclo[3.1.1]heptan-3-one
- CAS Number: 15358-88-0
- FEMA Number: Data not found
- Other Identifiers: FL number not found; CoE number not found; IFRA reference not found
- Molecular Formula: C10H16O
- Molecular Weight: 152.23 g/mol
cis-Isopinocamphone is a bicyclic monoterpene ketone. Its structure features a ketone functional group, which contributes to its characteristic odor profile. The bicyclic framework is crucial for its volatility and sensory attributes, influencing its role in both flavor and fragrance applications.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
cis-Isopinocamphone is known for its minty, camphoraceous odor with a slight woody undertone. It is often described as having a moderate intensity and a fresh, cooling character. The compound's odor threshold is not clearly reported, but it is typically used as an impact note in formulations, providing a refreshing and uplifting aroma.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
cis-Isopinocamphone is naturally found in essential oils such as rosemary and sage. It is formed through the oxidation of pinene derivatives, which are common in coniferous plants. This compound is relevant to "natural flavor" and "natural fragrance" designations due to its occurrence in these natural sources.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
cis-Isopinocamphone is utilized in flavor formulations for its minty and camphoraceous notes. It is commonly used in mint-flavored products, including chewing gums and confectioneries. Typical use levels in finished food products range from 0.5 to 5 ppm, with higher concentrations potentially leading to overpowering effects. The compound is relatively stable under normal processing conditions but may degrade under extreme heat or acidic conditions.
Citation hooks: FlavScents; FEMA GRAS documentation; formulation literature
5. Use in Fragrances
In the fragrance industry, cis-isopinocamphone is used in various fragrance families, including fougère and woody compositions. It serves as a modifier and impact note, contributing freshness and complexity. Typical concentration ranges in perfumes are from 0.1% to 1%, depending on the desired intensity. Its volatility allows it to function primarily as a top note, providing an initial burst of freshness.
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; no specific divergence noted.
- Asia: Limited specific data; generally follows international safety assessments.
- Latin America: No specific data; typically aligns with international standards.
Explicit approvals are not well-documented, and formulators should verify compliance with local regulations.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
- Oral Exposure: No specific ADI or MSDI values found; generally considered safe at typical flavor use levels.
- Dermal Exposure: No specific data on irritation or sensitization; IFRA guidelines should be consulted for fragrance use.
- Inhalation Exposure: Volatile nature suggests potential for inhalation exposure; occupational safety measures should be considered.
Risk profiles may differ slightly between food and fragrance applications, with dermal exposure being more relevant for fragrances.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
cis-Isopinocamphone is valued for its ability to impart a fresh, minty character to both flavors and fragrances. It synergizes well with other minty and herbal notes, enhancing overall freshness. Common pitfalls include overuse, leading to an overpowering camphoraceous effect. It is often under-utilized in complex fragrance compositions where subtle freshness is desired.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on cis-isopinocamphone is well-established in terms of its sensory profile and natural occurrence. However, specific regulatory approvals and toxicological data are less documented, requiring formulators to rely on industry-typical practices and 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 2026-09-28 12:16:12 GMT (p2)