Benzyl Salicylate in Perfumery | Première Peau
| Category | AROMA CHEMICALS |
| Subcategory | balsamic · floral · sweet |
| Origin | |
| Volatility | Base Note |
| Botanical | N/A — synthetic molecule |
| Appearance | Colorless to faint yellow viscous liquid with mild balsamic odor |
| Odor Strength | Low |
| Producing Countries | Manufactured globally |
| Pyramid | Base |
Almost nothing on the smelling strip — a whisper of clean warmth, sun-warmed cotton, the faintest balsamic sweetness. Many people cannot smell it at all. Yet remove it from a formula and the entire structure collapses: notes scatter, projection flattens, the fragrance dies in minutes. Benzyl salicylate is perfumery's invisible architecture.
Scent
Evolution over time
Immediately
After a few hours
After a few days
The Full Story
Did You Know?
Extraction & Chemistry
Extraction method: Produced synthetically by esterification of salicylic acid with benzyl alcohol under acid catalysis (sulfuric acid or acidic resin), at 100–120°C. Water is removed continuously to drive the reaction to completion. Industrial variants include solid-liquid phase-transfer catalysis using sodium salicylate and benzyl chloride (PEG-4000 catalyst, 150°C, yielding 96% at 99.5% purity). Also produced by transesterification of methyl salicylate with benzyl alcohol over metal oxide catalysts. Found naturally in jasmine absolute, ylang-ylang essential oil (Cananga odorata), carnation absolute, and neroli oil, but commercial supply is exclusively synthetic.
| Molecular Formula | C₁₄H₁₂O₃ |
| CAS Number | 118-58-1 |
| Botanical Name | N/A — synthetic molecule |
| IFRA Status | Restricted: IFRA 51st Amendment — concentration limits by product category (approx. 7–8% max in fine fragrance, 0.5% in lip products). EU Cosmetics Regulation 1223/2009 Annex III: mandatory label declaration above 0.001% in leave-on products, 0.01% in rinse-off. Classified as a weak sensitizer. SCCS final opinion (2024) found no conclusive evidence of endocrine disruption at normal use concentrations. |
| Synonyms | BENZYL 2-HYDROXYBENZOATE · SALICYLATE DE BENZYLE |
| Physical Properties | |
| Odor Strength | Low |
| Lasting Power | 384 hours at 100% |
| Appearance | Colorless to faint yellow viscous liquid with mild balsamic odor |
| Boiling Point | 208.00 °C. @ 26.00 mm Hg |
| Flash Point | 356.00 °F. TCC ( 180.00 °C. ) |
| Specific Gravity | 1.17600 to 1.18000 @ 25.00 °C. |
| Refractive Index | 1.57900 to 1.58300 @ 20.00 °C. |
| Melting Point | 22.00 to 25.00 °C. @ 760.00 mm Hg |
In Perfumery
Fixative, blender, and volume builder. Benzyl salicylate operates in the deep base of a composition, slowing evaporation and extending the life of volatile materials above it. Substantivity of 384 hours at full concentration. Used at 5–15% of formula weight — one of the highest-dosage single materials in commercial perfumery. Critical in white flower accords: jasmine, frangipani, ylang-ylang, tuberose. In jasmine reconstructions, it forms the balsamic-floral scaffold alongside benzyl acetate, indole, and methyl jasmonate. In modern musks and skin scents, its subliminal warmth contributes to the clean-skin effect. Related salicylates serve different roles: hexyl salicylate (CAS 6259-76-3) is greener, more transparent, used in fresh florals and ozonic accords. Phenylethyl salicylate (CAS 87-22-9) is heavier, more balsamic, used in orchid and heavy oriental bases. Amyl salicylate brings a solar, almost coconut-adjacent warmth to tropical accords. Benzyl salicylate appears in the formulation of Insuline Safrine (/products/insuline-safrine-saffron-perfume), where it likely contributes to the warm, intimate base that carries the saffron and gourmand notes.
See Also
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