Butylated hydroxytoluene (CAS 128-37-0) — Woody N/A Note Fragrance Ingredient

Woody · Citrus

Butylated hydroxytoluene

CAS 128-37-0

Origin
synthetic
Note
N/A
IFRA
Use with awareness
Data as of: Apr 2026

What Is Butylated hydroxytoluene?

Butylated hydroxytoluene (BHT) is a synthetic antioxidant commonly found in processed foods, cosmetics, and pharmaceuticals. It prevents rancidity by inhibiting oxidation. While ubiquitous in consumer products, BHT has sparked debate about its safety profile at high concentrations, making it a regulated ingredient in many applications.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for use in food and cosmetics
Potential endocrine disruptor at high doses
CAS
128-37-0
Formula
Mixture
MW
Variable
Odor Family
Woody · Citrus
Layer 1 · Enthusiast

What Does Butylated hydroxytoluene Smell Like?

BHT has a faint phenolic odor reminiscent of old books or printer ink. Its scent profile is dry and slightly medicinal, with a waxy undertone that lingers subtly. In formulations, it behaves more as a stabilizer than a fragrance note, though it can contribute a faintly chemical top note that dissipates quickly.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

N/A(N/A, 0)

N/A

Layer 2

2D Molecular Structure

Dibutyl paracresol

SMILES: CC1=CC(=C(O)C(=C1)C(C)(C)C)C(C)(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

BHT is a synthetic phenolic antioxidant belonging to the class of hindered phenols. It is produced industrially by the alkylation of p-cresol with isobutylene. The molecule’s effectiveness comes from its ability to donate hydrogen atoms to free radicals, terminating oxidation chain reactions. Its symmetrical structure and tert-butyl groups provide steric hindrance that enhances stability.

Physical & Chemical Properties

Boiling Point265 °C
Melting Point70 °C
Density1.048 g/cm³

Perfumer Guide

Note Position
N/A
Volatility
N/A
Blending
N/A
ApplicationTypical %RangeNotes
Food Preservation0.02%Up to 0.1%Prevents rancidity in fats and oils
Cosmetics0.1%Up to 0.5%Antioxidant in creams and lipsticks

Classic Accords

Tip: Use minimal quantities as stabilizer rather than fragrance component.

Alternatives & Comparisons

1
Tocopherol CAS 59-02-9

Natural antioxidant alternative derived from vitamin E, preferred in clean beauty formulations.

2
Rosemary Extract CAS N/A

Plant-derived antioxidant complex with additional aromatic benefits.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

Not restricted by IFRA but subject to regional limits in food and cosmetic applications.

EU Allergen Declaration

Not classified as an EU allergen.

GHS Classification

H315 Skin irritation H319 Eye irritation H335 May cause respiratory irritation

RIFM Assessment

RIFM has evaluated BHT as safe at current use levels in fragrances.

Sustainability

As a petrochemical derivative, BHT raises sustainability concerns. Manufacturers are increasingly replacing it with plant-derived antioxidants in response to consumer demand for cleaner ingredients. Proper disposal is required to prevent environmental persistence.

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References

  1. PubChem. Butylated hydroxytoluene. PubChem CID 31404

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

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Ingredient Data Sheet

CAS 128-37-0

Physical Properties

Molecular Weight220.35 g/mol🔬 PubChem
LogP (Octanol-Water)5.3🔬 PubChem
Boiling Point265 °C🔬 EPA CompTox
Vapor Pressure0.01 mmHg @ 25°C📊 OPERA
Flash Point126.7 °C🔬 EPA CompTox
Involatility Index0.0007💻 Calculated
log Kp (skin permeability)-0.281💻 Calculated
SMILESCC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorscitruswoody• leffingwell
Functional Groupsphenolaromatic💻 RDKit
BHA and BHT (butylated hydroxytoluene) are monohydric phenolic antioxidants that, prior to their introduction and acceptance in the food industry, were used to protect petroleum against oxidative degumming. BHT has a very faint, musty, occasional cresylictype odor. BHA and BHT are extensively used in foods as antioxidants. Most fats, oils and fat-containing foods are naturally susceptible to rapid rancification and other oxidative reactions that produce compounds having objectionable taste and odor, making foods containing them unpalatable. Lipid oxidation is autocatalytic and proceeds as a complex of chain reactions, the nature and speed of which vary with the substrate, temperature, light, availability of oxygen and presence or absence of oxidation catalysts. Antioxidants like BHT act as “chain breaks” in the autooxidation processes under the usual conditions of processing, storage and use of fat-containing foods (Burdock, 1997).📖 Fenaroli
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: DTXSID2020216

Physical Properties

Molecular Weight 220.356 g/mol🔬 EPA CompTox
Density 0.986 g/cm^3🔬 EPA CTX
Boiling Point 265.167 °C🔬 EPA CTX
Melting Point 70.384 °C🔬 EPA CTX
Flash Point 124.518 °C🔬 EPA CTX
Refractive Index 1.499 Dimensionless📊 OPERA
Molar Volume 237.514 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 5.007 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 5.086 Log10 unitless📊 OPERA
LogD (pH 7.4) 5.086 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.29 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0.003 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.011 mmHg🔬 EPA CTX
Surface Tension 30.031 dyn/cm📊 OPERA
Thermal Conductivity 111.008 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 20.23 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 69.734 cm^3/mol📊 OPERA
Polarizability 27.645 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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