HomeGlossary › Benzyl Salicylate

Benzyl Salicylate in Perfumery | Première Peau

AROMA CHEMICALS  /  balsamic · floral · sweet
Benzyl Salicylate
Benzyl Salicylate perfume ingredient
CategoryAROMA CHEMICALS
Subcategorybalsamic · floral · sweet
Origin
VolatilityBase Note
BotanicalN/A — synthetic molecule
AppearanceColorless to faint yellow viscous liquid with mild balsamic odor
Odor StrengthLow
Producing CountriesManufactured globally
PyramidBase

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.

  1. Scent
  2. The Full Story
  3. Fun Fact
  4. Extraction & Chemistry
  5. In Perfumery
  6. See Also

Scent

Almost imperceptible on its own. What registers is less a smell than a sensation: warm, clean, faintly powdery, with a distant balsamic sweetness recalling sun-heated skin. Softer than benzyl benzoate, less green than hexyl salicylate, without the coumarinic sweetness of amyl salicylate. Some perceive a vague muskiness. Others smell nothing at all. Its substantivity is extreme — 384 hours at 100% concentration — which explains its role as a fixative that outlasts nearly everything around it.

Evolution over time

Immediately

Immediately

After a few hours

After a few hours

After a few days

After a few days

The Full Story

Benzyl salicylate (CAS 118-58-1, C₁₄H₁₂O₃, MW 228.25) is the benzyl ester of salicylic acid. Colorless to pale yellow viscous liquid, melting near room temperature (22–25°C), with a LogP of 4.21 — meaning strong affinity for oils and poor water solubility. Its odor is peculiar: most descriptions say warm, faintly balsamic, vaguely floral. But a significant portion of the population is specifically anosmic to it. The perfumer Guy Robert reportedly could not smell benzyl salicylate at all, yet could detect its presence in any composition by the way it shaped everything around it.

Despite near-imperceptibility, it is a consumed aroma chemicals in the industry. Used routinely at 5–15% of a formula — sometimes higher — it functions as fixative, blender, and volume builder. It slows evaporation of volatile top notes, smooths transitions between heart and base, and lends a diffuse, radiant quality to florals. It is the backbone of jasmine reconstructions and appears naturally in jasmine absolute, ylang-ylang oil, carnation, and neroli.

Its UV-absorbing properties made it a protagonist in early sunscreen history. In 1935, Eugène Schueller used benzyl salicylate as the active UV filter in the first mass-market sun oil, later known as Ambre Solaire. The molecule absorbs UVB radiation effectively, though it was eventually replaced by more potent filters.

Regulated under EU Cosmetics Regulation 1223/2009 as one of the 26 designated allergens requiring label declaration above 0.001% in leave-on products. The SCCS assessed potential endocrine-disrupting concerns and concluded no observable endocrine effects at normal use concentrations. IFRA restricts it under the 51st Amendment with category-specific limits (approximately 7–8% in fine fragrance). It belongs to the salicylate family alongside hexyl salicylate (greener, more transparent), phenylethyl salicylate (heavier, more balsamic), and amyl salicylate (solar, tropical).

Did You Know?

Did you know?
In 1935, Eugène Schueller — founder of what became the world's largest cosmetics company — formulated the first mass-market sun oil using benzyl salicylate as its active UV filter. The product was marketed as Ambre Solaire and claimed to tan skin five times faster without burning. Benzyl salicylate thus has the distinction of being both perfumery's most invisible ingredient and one of the first molecules deliberately placed between human skin and sunlight.

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 FormulaC₁₄H₁₂O₃
CAS Number118-58-1
Botanical NameN/A — synthetic molecule
IFRA StatusRestricted: 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.
SynonymsBENZYL 2-HYDROXYBENZOATE · SALICYLATE DE BENZYLE
Physical Properties
Odor StrengthLow
Lasting Power384 hours at 100%
AppearanceColorless to faint yellow viscous liquid with mild balsamic odor
Boiling Point208.00 °C. @ 26.00 mm Hg
Flash Point356.00 °F. TCC ( 180.00 °C. )
Specific Gravity1.17600 to 1.18000 @  25.00 °C.
Refractive Index1.57900 to 1.58300 @  20.00 °C.
Melting Point22.00 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

Premiere Peau Perfumery Glossary. Explore all 75 ingredient entries