Synthetic Ingredient Overview
- 🔎 Chemical Name: γ-Nonalactone 
- 🧪 Synonyms: Aldehyde C-18, Coconut Lactone 
- 🧬 Chemical Formula: C₉H₁₆O₂ 
- 📂 CAS N°: 104-61-0 
- 📘 FEMA: 2783 
- ⚖️ MW: 156.22 g/mol 
- ♨️ Vapor Pressure (25 °C): ~1.18 × 10⁻² mm Hg (est.) 
- 📝 Odor Type: Fruity (Coconut) 
- 📈 Odor Strength: Medium-strong, with extreme longevity (approx. 300 hrs on blotter) 
- 👃🏼 Odor Profile: Intense coconut, creamy, fruity in high dilution, soft floral-musk undercurrent 
- 👅 Flavor Profile: Coconut, sweet nutty, used in fruit and dessert-type flavors 
- ⚗️ Uses: Floral volume builder, lactonic booster in white florals, coconut flavor agent, fixative 
- 🧴 Appearance: Colorless to pale yellow liquid 
What is Gamma-Nonalactone?
Gamma-Nonalactone, often mistakenly referred to as “Aldehyde C-18,” is a γ-lactone — a cyclic ester — derived from nonanoic acid. Despite the name confusion, it is chemically distinct from aldehydes. First reported in the 1920s and widely used since the 1950s, it became a staple in perfumery for its tropical, creamy, and long-lasting coconut character.
Structurally, it is a medium-sized ring lactone with significant volatility and diffusiveness for a base note compound. Its intense sweetness and tropical warmth allow it to function as both a fruity top enhancer and a long-wearing base material.
Olfactory Profile & Perfumery Applications
Gamma-Nonalactone adds unmistakable coconut warmth to both floral and Oriental compositions. Its use must be measured carefully: while trace amounts yield a creamy sweetness, even moderate overdosing can overpower compositions with lactonic heaviness.
Notable applications:
- White Floral Bases: Enhances Gardenia, Jasmine, Tuberose, Honeysuckle, Plumeria 
- Oriental & Musky Accords: Used with Sandalwood, Styrax, Musk, and Undecanolide 
- Coconut Accords: Core component in beachy tropical profiles 
- Fixative Role: Contributes depth and longevity to fruity and creamy blends 
Typical usage levels range between 0.01% and 0.3% in fine fragrance. In functional applications (candles, soaps), levels may be adjusted for thermal or surfactant resistance.
Industrial & Technical Uses
- Fine Fragrance: Coconut-floral accords, exotic sweet notes, solar blends 
- Functional Fragrance: Long-lasting odor masking in detergents, personal care 
- Flavor Use (FEMA 2783): Used at 10–50 ppm in tropical, coconut, cherry, or nut flavors 
- Industrial Synthesis: Key building block in lactonic structures, low-odor solvents 
Regulatory & Safety Overview
- IFRA Status (2023): No specific restrictions; evaluated as standard lactone 
- EU Allergens (1223/2009): Not among 26 declarable allergens 
- REACH: Registered 
- ECHA Classification: Not classified as hazardous 
- FEMA GRAS Status: FEMA No. 2783 — Approved for flavor use 
- Toxicology: Low acute toxicity; not sensitizing under controlled levels 
✅ Safe under normal usage conditions. Overuse may cause cloying odor profiles; not phototoxic or carcinogenic under typical perfumery exposure.
Natural Occurrence
Gamma-Nonalactone has been reported in a wide variety of natural matrices, including:
- Fruits: Peach, Apricot, Papaya, Guava, Currant, Strawberry, Raisin 
- Fermented Products: Rum, Whiskey, Wine, Sherry, Beer 
- Animalic Foods: Chicken, Pork, Beef fat, Butter, Cheese 
- Others: Camembert, Tomato, Soybean, Green Tea, Rice, Malt, Sweetgrass 
Despite these occurrences, commercial use is almost entirely synthetic, due to isolation cost.
Production Methods
- From Nonanoic Acid: Lactonization via acid catalysis 
- Via Hexanol + Methyl Acrylate: Free-radical route using di-tert-butylperoxide 
- From Undecylenic Acid + Malonic Acid: Alternate multi-step esterification 
These routes allow scalable, cost-effective industrial supply for both flavor and fragrance use.
Sources
- Symrise Technical Literature 
- Perfume and Flavor Chemicals – S. Arctander (1969) 
- Fenaroli’s Handbook of Flavor Ingredients 
- Monographs on Fragrance Raw Materials – D. L. J. Opdyke (RIFM) 
- Leffingwell Chirality Database 
- PubChem – Compound CID 7792 
- Scentspiracy Internal Research – Fulvio Ciccolo (2024) 
 
         
         
    
    
      
      
        
      
      
    
      
      
        
          
        
      
      
        
        
          
        
        
 
      
    
   
    
    
      
      
        
      
      
    
      
      
        
          
        
      
      
        
        
          
        
        
 
      
    
   
    
    
      
      
        
      
      
    
      
      
        
          
        
      
      
        
        
          
        
        
 
      
    
   
    
    
      
      
        
      
      
    
      
      
        
          
        
      
      
        
        
          
        
        
 
      
    
   
    
    
      
      
        
      
      
    
      
      
        
          
        
      
      
        
        
          
        
        
 
      
    
      
      
        
          
        
      
      
        
        
          
        
        
