3-Butylidenephthalide (CAS 0551-08-06) — Green Middle Note Fragrance Ingredient

Green · Woody

3-Butylidenephthalide

CAS 0551-08-06

Origin
synthetic
Note
Middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is 3-Butylidenephthalide?

3-Butylidenephthalide is a synthetic fragrance compound used in perfumery to create unique aromatic profiles. It’s not commonly encountered in everyday products but may appear in niche fragrances. This ingredient matters because it offers perfumers a distinctive tool for crafting complex, unconventional scent compositions that stand out in the market.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Limited safety data available
Use at low concentrations
CAS
0551-08-06
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 3-Butylidenephthalide Smell Like?

3-Butylidenephthalide presents a sharp, herbaceous character with a celery-like rootiness that evolves into a warm, slightly spicy heart. The dry-down reveals a subtle woody undertone with a lingering earthy persistence. Its odor profile is reminiscent of crushed green stems with a faint metallic edge, making it useful for creating vegetal accents in avant-garde compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Synthetic Jungle(Frederic Malle, 2021)

Used as a green-modifier to enhance the hyper-realistic foliage effect, contributing a crisp, stem-like quality to the galbanum and oakmoss base.

Eau de Campagne(Sisley, 1973)

Provides a modern vegetal twist to this classic green floral, amplifying the tomato leaf accord with its distinctive celery-like character.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3-Butylidenephthalide belongs to the phthalide class of compounds, structurally related to lactones. While found in trace amounts in some natural sources like celery, commercial production is typically synthetic. The molecule features a butylidene side chain attached to a phthalide core, creating its distinctive odor characteristics. Synthesis often involves condensation reactions of appropriate phthalic acid derivatives with butyraldehyde precursors.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor ThresholdVery low (high potency)

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Specialized
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used as an accent note
Functional Fragrance0.01-0.1%Trace amountsFor green nuances

Classic Accords

+ Galbanum + Violet Leaf = Hyper-green + Oakmoss + Patchouli = Dark vegetal

Tip: Use sparingly in green compositions to add dimension without overwhelming the blend.

Alternatives & Comparisons

1
Sedanolide CAS 54814-64-1

Offers similar celery-like characteristics but with greater diffusion and a smoother profile.

2
Dihydrocoumarin CAS 119-84-6

Provides herbaceous-tonka nuances when a sweeter green character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions. General usage guidelines apply due to limited safety data.

RIFM Assessment

Not currently evaluated by RIFM. Use with caution pending further safety assessment.

Sustainability

As a synthetic material, 3-Butylidenephthalide has minimal environmental impact in production compared to natural extracts. Its high potency means small quantities are effective, reducing overall material usage. The synthetic route avoids agricultural land use and seasonal variability associated with natural sources.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Allured Publishing.

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

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