Allyl (2-methylbutoxy)acetate (CAS 67634-01-09) — Green Top to middle Note Fragrance Ingredient

Green · Floral

Allyl (2-methylbutoxy)acetate

CAS 67634-01-09

Origin
synthetic
Note
Top to middle
IFRA
Generally safe
Data as of: Apr 2026

What Is Allyl (2-methylbutoxy)acetate?

Allyl (2-methylbutoxy)acetate is a synthetic fragrance ingredient used to create fruity, green, and slightly floral notes in perfumes and scented products. You’ll encounter it in modern floral-fruity compositions, particularly those aiming for a fresh, crisp character. This molecule matters because it offers perfumers a versatile tool for building contemporary accords that bridge fruity top notes with floral heart notes, often contributing to fragrances that smell both natural and innovative.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Limited safety data – use standard precautions
CAS
67634-01-09
Formula
Mixture
MW
Variable
Odor Family
Green · Floral
Layer 1 · Enthusiast

What Does Allyl (2-methylbutoxy)acetate Smell Like?

Allyl (2-methylbutoxy)acetate opens with a bright, crisp green apple note that quickly evolves into a juicy pear-like character. The heart reveals a delicate floralcy reminiscent of lily-of-the-valley, with a subtle tropical nuance. As it dries down, it maintains a clean, slightly woody-fruity character that blends seamlessly with other notes. The overall effect is like biting into a perfectly ripe Bartlett pear while standing in a sunlit orchard – fresh, aqueous, and subtly sweet without being cloying.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Green Tea(Elizabeth Arden, 1999)

Used here to enhance the crisp, refreshing top notes, contributing to the fragrance’s signature ‘just-brewed’ tea leaves character while adding subtle fruity nuances.

Light Blue(Dolce & Gabbana, 2001)

Provides the juicy pear-like facets that complement the citrus opening, helping create the fragrance’s distinctive Mediterranean freshness.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Allyl (2-methylbutoxy)acetate is an ester formed from allyl alcohol and 2-methylbutoxyacetic acid. As a synthetic material, it’s typically produced via esterification reactions under acidic conditions. The branched alkyl chain contributes to its unique fruity-green odor profile. While not found in nature, its structural elements mimic those found in various fruit esters, allowing it to blend naturally with botanical extracts despite being wholly synthetic.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor StrengthMedium

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Fresh fruity-floral modifier
Functional Fragrance0.1-1%Up to 3%Adds crispness to fruity compositions

Classic Accords

Tip: Use to bridge citrus top notes with floral heart notes in modern fresh florals.

Alternatives & Comparisons

1
Allyl amyl glycolate CAS 67634-00-8

Offers similar fruity-green effects but with more pronounced tropical pineapple nuances and greater tenacity.

2
Hexyl acetate CAS 142-92-7

Provides a simpler pear-like note when a less complex fruity character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA standards.

RIFM Assessment

Not currently evaluated by RIFM – treat as new chemical entity.

Sustainability

As a synthetic material, Allyl (2-methylbutoxy)acetate has minimal environmental impact from sourcing. Production typically uses petrochemical feedstocks, but its high potency means small quantities are effective. No known issues with biodegradability, though full ecotoxicological profile remains to be established.

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References

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

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

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