2,6-Dimethyloct-7-en-2-yl formate (CAS 25279-09-08) — Citrus Top Note Fragrance Ingredient

Citrus · Green

2,6-Dimethyloct-7-en-2-yl formate

CAS 25279-09-08

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

What Is 2,6-Dimethyloct-7-en-2-yl formate?

2,6-Dimethyloct-7-en-2-yl formate is a synthetic fragrance ingredient used to create fresh, fruity, and slightly green top notes in perfumes. You’ll encounter it in modern citrusy and floral fragrances, often lending a crisp, uplifting quality. This molecule matters because it can mimic natural freshness while offering superior stability in formulations. Its synthetic nature allows for consistent quality and ethical sourcing compared to some natural alternatives.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions reported
Limited safety data available
CAS
25279-09-08
Formula
Mixture
MW
Variable
Odor Family
Citrus · Green
Layer 1 · Enthusiast

What Does 2,6-Dimethyloct-7-en-2-yl formate Smell Like?

A breezy, dewy freshness opens with the shimmer of crushed green apple skins and unripe pineapple. The heart reveals a subtle floralcy reminiscent of lily-of-the-valley petals touched by morning dew, while the dry-down carries a whisper of freshly cut stems. Unlike sharper citrus top notes, this molecule maintains a rounded, almost aqueous quality that blends seamlessly with both fruity and floral compositions, never dominating but always lifting.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Aqua Universalis(Maison Francis Kurkdjian, 2009)

Used here to amplify the citrus top while preventing excessive sharpness, creating the illusion of mountain spring water flowing through white flowers.

Light Blue(Dolce & Gabbana, 2001)

Provides the crisp ‘just-peeled citrus’ effect that makes this fragrance so instantly recognizable, blending with Sicilian lemon for added dimensionality.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

This branched-chain formate ester belongs to the terpenoid family, structurally related to natural compounds found in citrus peels. Industrial synthesis typically involves esterification of the corresponding alcohol with formic acid under controlled conditions. The molecule’s chirality at multiple centers contributes to its nuanced olfactory profile – the racemic mixture used commercially offers broader application versatility than isolated enantiomers might achieve.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top
Volatility
Medium (1-2 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Fresh top note component
Functional Fragrance0.5-1%Up to 2%Air care applications

Classic Accords

Tip: Use to bridge citrus and floral notes while preventing harshness in high-impact fresh fragrances.

Alternatives & Comparisons

1
Linalyl formate CAS 115-99-1

For a more floral, bergamot-like character with similar fresh properties but lower tenacity.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No current IFRA restrictions

RIFM Assessment

Not currently assessed by RIFM

Sustainability

As a synthetic material, production avoids agricultural land use but depends on petrochemical feedstocks. Modern manufacturing processes typically employ green chemistry principles to minimize waste and energy consumption. Unlike some natural alternatives, this material doesn’t contribute to deforestation or habitat loss.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. ISBN 9783527619580

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

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