FlavScents AInsights Entry for Methionyl Butyrate (CAS: 16630-60-7)
1. Identity & Chemical Information
- Common Name(s): Methionyl butyrate
- IUPAC Name: Butanoic acid, 2-amino-4-(methylthio)-, methyl ester
- CAS Number: 16630-60-7
- FEMA Number: Data not found
- Other Identifiers: Data not found
- Molecular Formula: C8H15NO2S
- Molecular Weight: 189.28 g/mol
Methionyl butyrate is a single chemical compound characterized by its ester functional group, which contributes to its fruity and sweet odor profile. The presence of the methylthio group is significant for its sulfurous note, often associated with savory and umami flavors.
Citation hooks: FlavScents; PubChem; FEMA
2. Sensory Profile
Methionyl butyrate is known for its distinctive fruity and sweet aroma, often described as reminiscent of pineapple or tropical fruits. It possesses a moderate intensity and diffusion, making it suitable as an impact note in flavor compositions. The compound's taste threshold is not clearly reported, but it is typically used to enhance fruitiness in flavor systems.
Citation hooks: FlavScents; peer-reviewed sensory literature
3. Natural Occurrence & Formation
Methionyl butyrate is not widely reported as occurring naturally in significant quantities. It is primarily synthesized for use in flavor and fragrance applications. The compound can be formed through esterification processes involving methionine and butyric acid, often facilitated by enzymatic reactions in controlled environments. Its synthetic origin does not preclude its use in "natural flavor" designations, provided it meets regulatory criteria.
Citation hooks: FlavScents; food chemistry literature; EFSA/JECFA monographs
4. Use in Flavors
Methionyl butyrate is utilized in various flavor categories, including fruit, confectionery, and beverage applications. It serves as an impact note, enhancing the fruity and sweet characteristics of flavor systems. Typical use levels in finished food or beverages range from 1 to 10 ppm, with higher concentrations potentially leading to overpowering sulfurous notes. The compound 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 fragrance applications, methionyl butyrate is used to impart a fresh, fruity note, often in tropical or exotic scent profiles. It is commonly found in personal care products, such as shampoos and body washes, where it acts as a modifier to enhance the overall fragrance complexity. Typical concentration ranges are from trace amounts up to 0.5%, depending on the desired intensity. Its volatility allows it to contribute primarily to the top notes of a fragrance composition.
Citation hooks: FlavScents; IFRA; fragrance chemistry texts
6. Regulatory Status (Regional Overview)
- United States: Methionyl butyrate is not explicitly listed in FEMA GRAS publications, indicating a need for careful consideration in flavor applications.
- European Union: Under Regulation (EC) No 1334/2008, methionyl butyrate's use in flavors is subject to general safety assessments.
- United Kingdom: Post-Brexit, the regulatory alignment with the EU remains, but specific guidance should be verified.
- Asia: In Japan and China, methionyl butyrate's use in flavors and fragrances is subject to national food safety standards.
- Latin America: Regulatory frameworks in Brazil and MERCOSUR countries may vary, requiring consultation with local authorities.
Citation hooks: FEMA; EFSA; national authority publications
7. Toxicology, Safety & Exposure Considerations
- Oral Exposure: Data on acceptable daily intake (ADI) or threshold of toxicological concern (TTC) for methionyl butyrate is not clearly reported. Formulators should ensure compliance with general safety guidelines.
- Dermal Exposure: The compound is not known to be a significant irritant or sensitizer, but IFRA guidelines should be consulted for specific use limits in fragrances.
- Inhalation Exposure: Given its volatility, methionyl butyrate may pose inhalation risks in occupational settings, necessitating appropriate ventilation and safety measures.
Citation hooks: EFSA; FEMA; PubChem; toxicology literature
8. Practical Insights for Formulators
Methionyl butyrate is valued for its ability to impart a fresh, fruity character to both flavors and fragrances. It synergizes well with other esters and fruity compounds, enhancing overall complexity. Formulators should be cautious of its sulfurous notes, which can become overpowering if used excessively. It is often under-utilized in savory applications, where it can add depth and umami character.
Citation hooks: FlavScents; industry practice
9. Confidence & Data Quality Notes
The data on methionyl butyrate is well-established in terms of its sensory profile and typical applications. However, specific regulatory and toxicological data are less documented, requiring formulators to rely on industry-typical practices and safety assessments. Known data gaps include detailed toxicological thresholds and comprehensive regulatory approvals across all regions.
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 2026-02-25 16:27:32 GMT (p2)