Ferulic Acid (CAS 1135-24-6) — Spicy Heart Note Fragrance Ingredient

spicy vanilla

Ferulic Acid

CAS 1135-24-6

Origin
natural
Note
IFRA
Generally safe
Data as of: Mar 2026

What Is Ferulic Acid?

Ferulic acid is a natural compound found in plant cell walls, especially in grains like rice and wheat, and also in coffee beans. You encounter it in whole grain foods, some skincare products, and as a subtle background note in fragrances. This ingredient matters because it acts as a natural antioxidant in both foods and cosmetics, and provides a warm, spicy-vanilla nuance to perfumes that bridges between sweet and woody accords.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Naturally occurring antioxidant
No significant restrictions
CAS
1135-24-6
Formula
C10H10O4
MW
194.18
Odor Family
spicy vanilla
Ferulic Acid 2D structure
Ferulic Acid
C10H10O4
Layer 1 · Enthusiast

What Does Ferulic Acid Smell Like?

Ferulic acid offers a delicate interplay of warm spices and sun-baked vanilla pods, with a subtle phenolic edge reminiscent of clove stems. Its dry, powdery texture evolves into a soft woody-amber dry down, behaving like a quiet conductor that amplifies surrounding notes. In dilution, it reveals a hay-like sweetness akin to coumarin’s distant cousin, but with more vegetal depth – like vanilla infused with the sap of young oak trees.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Santal Blush(Tom Ford, 2011)

Used as a bridge between spicy top notes and creamy sandalwood base, adding a wheat-like warmth that prevents the composition from becoming too sweet.

Bois d'Argent(Dior, 2004)

Ferulic acid’s grain-like facets enhance the fragrance’s distinctive ‘blond woods’ accord, contributing to its luminous, sunlit quality.

Layer 2

2D Molecular Structure

Ferulic acid

SMILES: COC1=C(O)C=CC(C=CC(O)=O)=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Ferulic acid is a hydroxycinnamic acid derivative, part of the phenylpropanoid class of plant metabolites. Naturally esterified to arabinoxylans in plant cell walls, it’s released during digestion or processing. Industrially produced via alkaline hydrolysis of agricultural byproducts or synthesized from vanillin. The trans-isomer (E-configuration) is more stable and prevalent than the cis-form. Its phenolic hydroxyl and carboxylic acid groups make it moderately polar (TPSA 66.8 Ų), while the conjugated π-system allows UV absorption – explaining its use in photoprotective cosmetics.

Physical & Chemical Properties

Melting Point168-171 °C
Molecular Weight194.18 g/mol
XLogP1.5
Vapor Pressure2.69×10⁻⁶ mmHg

Perfumer Guide

Note Position
Heart-to-base
Volatility
Moderate (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Background modifier
Functional Fragrance0.01-0.1%Up to 0.3%Antioxidant side-benefit

Classic Accords

+ Vanilla + Benzoin = Spiced resin + Coumarin + Tonka = Hay absolute effect

Tip: Use to add dryness to overly sweet vanillic compositions – blends particularly well with ionones.

Alternatives & Comparisons

1
p-Coumaric Acid CAS 7400-08-0

Less methoxy character, more direct honey-like sweetness when higher concentrations are needed.

2
Dihydroferulic Acid CAS 1135-23-5

Hydrogenated version with softer, more powdery character and reduced phenolic sharpness.

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 IFRA restrictions – not classified as sensitizing in current guidelines.

RIFM Assessment

RIFM-reviewed and deemed safe at current usage levels in fragrances (2015 assessment).

Sustainability

Primarily sourced as a byproduct of rice bran oil production or from wheat bran, making its extraction relatively sustainable. Synthetic production exists but is less common due to availability of plant-derived material. As an antioxidant, it can reduce need for synthetic preservatives in formulations.

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References

  1. PubChem CID 445858 Ferulic Acid
  2. Graf E. (1992). Antioxidant potential of ferulic acid. Free Radical Biology and Medicine. PMID 1334049

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

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Ingredient Data Sheet

CAS 1135-24-6

Physical Properties

Molecular Weight194.18 g/mol🔬 PubChem
LogP (Octanol-Water)1.5🔬 PubChem
Boiling Point279 °C🔬 EPA CompTox
Vapor Pressure0 mmHg @ 25°C📊 OPERA
Flash Point150.5 °C🔬 EPA CompTox
log Kp (skin permeability)-2.819💻 Calculated
SMILESCOC1=C(C=CC(=C1)C=CC(=O)O)O🔬 PubChem

Volatility & Performance

Fragrance NoteBase💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score8.3 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsspicyvanilla• leffingwell
Functional Groupsphenoletheralkenearomatic💻 RDKit
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID5040673

Physical Properties

Molecular Weight 194.186 g/mol🔬 EPA CompTox
Density 1.331 g/cm^3📊 OPERA
Boiling Point 327.033 °C📊 OPERA
Melting Point 169.5 °C🔬 EPA CTX
Flash Point 150.55 °C🔬 EPA CTX
Refractive Index 1.627 Dimensionless📊 OPERA
Molar Volume 147.467 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.51 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 0.201 Log10 unitless📊 OPERA
LogD (pH 7.4) -1.621 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.07 Log10 unitless📊 OPERA
Water Solubility 0.007 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg🔬 EPA CTX
Viscosity 10.992 cP📊 OPERA
Surface Tension 48.797 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 66.76 Ų💻 Computed
H-Bond Donors 2 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 3 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 52.267 cm^3/mol📊 OPERA
Polarizability 20.72 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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