Amyl Salicylate (CAS 2050-08-0) — Sweet Base Note Fragrance Ingredient




Amyl Salicylate

CAS 2050-08-0

Origin
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Amyl Salicylate?

Amyl salicylate is a synthetic fragrance ingredient with a sweet, floral, and slightly herbal aroma. You’ll find it in perfumes, soaps, and air fresheners where it adds a fresh, clean character. This versatile molecule matters because it mimics natural floral notes while being more stable and affordable than plant extracts.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
IFRA approved with no restrictions
Potential mild skin sensitivity
CAS
2050-08-0
Formula
Mixture
MW
Variable
Odor Family
Layer 1 · Enthusiast

What Does Amyl Salicylate Smell Like?

Amyl salicylate opens with a crisp, green-floral burst reminiscent of clover fields at dawn. Within minutes, it evolves into a smooth, sweet heart resembling chamomile tea with honey. The dry-down reveals a soft, powdery-musky base that lingers like sun-warmed linen. Unlike sharper salicylates, its five-carbon chain adds roundness – imagine orchid petals dipped in pear nectar, with just a whisper of minty freshness keeping it from becoming cloying.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used as a floral modifier to soften the aldehydic sparkle and bridge the jasmine-rose heart with the woody base.

L’Air du Temps(Nina Ricci, 1948)

Provides a clean, soapy floralcy that complements the carnation and sandalwood, creating its signature ‘fresh laundry’ effect.

Layer 2

2D Molecular Structure

Pentyl 2-hydroxybenzoate

SMILES: CCCCCOC(=O)C1=C(O)C=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Amyl salicylate (pentyl 2-hydroxybenzoate) is an ester formed from salicylic acid and amyl alcohol. Industrially produced via Fischer esterification, it’s achiral with a benzene ring esterified to a five-carbon chain. The ortho-positioned hydroxyl group allows some intramolecular hydrogen bonding, influencing its volatility and tenacity. Modern synthesis often uses pentanol and salicylic acid with acid catalysts at 100-150°C.

Physical & Chemical Properties

Boiling Point 280-282 °C
Density 1.052 g/cm³
Flash Point >100 °C
Refractive Index 1.505-1.509

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-6 hours)
Blending
Very good
Application Typical % Range Notes
Fine Fragrance 1-5% Up to 10% Floral modifier/base
Soap 0.5-2% Up to 3% Provides lasting floralcy

Classic Accords

+ Lilial + Galaxolide = Clean floral
+ Citronellol + Phenethyl Alcohol = Rose bouquet

Tip: Use with ionones to create magnolia effects or with musks for skin-scent applications.

Alternatives & Comparisons

1
Benzyl Salicylate CAS 118-58-1

More tenacious with a heavier floral character; better for base notes when longer persistence is needed.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. IFRA, REACH, EU Cosmetics Regulation standards update periodically. Consult current IFRA Standards Library before formulating. Not legal or regulatory advice.

IFRA Status

No restrictions under IFRA 49th Amendment.

RIFM Assessment

RIFM evaluation confirms safe use at current industry levels.

Sustainability

Synthesized from petrochemical precursors, amyl salicylate has consistent quality and avoids agricultural land use. Production energy can be optimized via catalytic processes. Biodegradation occurs via ester hydrolysis, with moderate environmental persistence (EC50 Daphnia magna >100 mg/L).

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Industry & Science Data

Global Usage Rank
#16 most used
by global fragrance volume
Source: IFRA Usage Survey 2015
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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Mar 2026.

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Physicochemical Properties

DTXSID: DTXSID9029227

Physical Properties

Molecular Weight 208.257 g/mol🔬 EPA CompTox
Density 1.054 g/cm^3🔬 EPA CTX
Boiling Point 275.463 °C🔬 EPA CTX
Melting Point -11.9 °C🔬 EPA CTX
Flash Point 117.567 °C🔬 EPA CTX
Refractive Index 1.521 Dimensionless📊 OPERA
Molar Volume 191.783 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.567 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 3.694 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.649 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.75 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.002 mmHg🔬 EPA CTX
Viscosity 15.056 cP📊 OPERA
Surface Tension 39.446 dyn/cm📊 OPERA
Thermal Conductivity 146.685 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 46.53 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 5 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 58.439 cm^3/mol📊 OPERA
Polarizability 23.167 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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