Benzoic acid, 2-methyl-, methyl ester (CAS 89-71-4) — Sweet Middle Note Fragrance Ingredient

Sweet · Floral

Benzoic acid, 2-methyl-, methyl ester

CAS 89-71-4

Origin
synthetic
Note
Middle
IFRA
Generally safe
Data as of: Apr 2026

What Is Benzoic acid, 2-methyl-, methyl ester?

Methyl 2-methylbenzoate is a synthetic fragrance ingredient commonly found in perfumes and flavored products. It contributes a fruity, floral nuance reminiscent of ylang-ylang and strawberries. This ester is valued for its ability to enhance floral bouquets and add a subtle sweetness without overpowering other notes.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Approved for use in cosmetics
Avoid direct skin contact in pure form
CAS
89-71-4
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does Benzoic acid, 2-methyl-, methyl ester Smell Like?

Methyl 2-methylbenzoate opens with a bright, fruity burst reminiscent of ripe strawberries dipped in cream. As it evolves, the floral heart emerges – a delicate ylang-ylang character with hints of mimosa pollen. The dry-down reveals a soft, powdery muskiness that lingers close to the skin. Throughout its evolution, it maintains a candied sweetness like crystallized flower petals, making it particularly useful for enhancing floral compositions without becoming cloying.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used as a subtle modifier in the floral bouquet, adding candied nuances to the ylang-ylang and jasmine notes while preventing the aldehydes from becoming too sharp.

Miss Dior(Dior, 1947)

Provides a strawberry-like fruity facet to the chypre structure, bridging the gap between the citrus top notes and mossy base.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Methyl 2-methylbenzoate is an aromatic ester formed by the esterification of 2-methylbenzoic acid with methanol. As a synthetic material, it’s typically produced through acid-catalyzed Fischer esterification. The methyl group ortho to the ester functionality creates steric hindrance that influences both its reactivity and odor characteristics. While not found in significant quantities in nature, related methyl benzoates occur in various essential oils.

Physical & Chemical Properties

Boiling Point218-220 °C
Density1.082 g/cm³

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Floral modifier
Soap0.1-0.5%Up to 1%Adds fruity nuance

Classic Accords

Tip: Use in trace amounts to lift floral compositions and add dimensionality to fruity notes.

Alternatives & Comparisons

1
Methyl benzoate CAS 93-58-3

For a cleaner floral effect without the fruity nuances, though less tenacious.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions currently apply.

RIFM Assessment

Considered safe at current usage levels based on RIFM evaluation.

Sustainability

As a synthetic material, methyl 2-methylbenzoate has minimal environmental impact in production. Its efficient synthesis from readily available precursors makes it a sustainable choice compared to some natural alternatives that require extensive plant cultivation.

Explore Benzoic acid, 2-methyl-, methyl ester

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press. ISBN 9781420090772

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

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