3,7-Dimethyloct-6-enyl acetate (CAS 67601-05-02) — Citrus Top to Middle Note Fragrance Ingredient

Citrus · Floral

3,7-Dimethyloct-6-enyl acetate

CAS 67601-05-02

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

What Is 3,7-Dimethyloct-6-enyl acetate?

3,7-Dimethyloct-6-enyl acetate is a synthetic fragrance ingredient with a fresh, floral-citrus character. It’s commonly found in personal care products like shampoos, soaps, and body sprays. This versatile material helps create natural-smelling floral bouquets while adding diffusion and lift to fragrance compositions.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Not restricted by IFRA
Limited safety data available
CAS
67601-05-02
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does 3,7-Dimethyloct-6-enyl acetate Smell Like?

3,7-Dimethyloct-6-enyl acetate opens with a bright, sparkling citrus-lime top note reminiscent of freshly peeled bergamot zest. This quickly evolves into a floral heart with rose-like facets and a subtle green undertone. The dry-down reveals a clean, woody-musky base with excellent tenacity. The overall effect is fresh yet sophisticated, combining the vibrancy of citrus with the elegance of white florals.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Dynamisante(Clarins, 1987)

Used as a citrus-floral bridge between bergamot top notes and herbal heart notes, adding diffusion and natural freshness to this energizing cologne.

CK One(Calvin Klein, 1994)

Provides a clean, modern floralcy that complements the green tea and papaya notes, helping create the fragrance’s signature unisex appeal.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3,7-Dimethyloct-6-enyl acetate is a monoterpenoid ester synthesized through acetylation of the corresponding alcohol (3,7-dimethyloct-6-en-1-ol). The molecular structure features a branched carbon chain with a terminal double bond and acetate group, contributing to its moderate volatility and fresh-floral odor characteristics. Industrial synthesis typically involves catalytic hydrogenation of citronellol followed by acetylation.

Physical & Chemical Properties

Boiling PointApprox. 220-230 °C (estimated)
DensityApprox. 0.88-0.90 g/cm³ (estimated)

Perfumer Guide

Note Position
Top to Middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Adds freshness in floral compositions
Personal Care0.5-3%Up to 5%Used in shower gels, deodorants

Classic Accords

Tip: Use in citrus-floral bases to add diffusion and natural freshness without excessive sweetness.

Alternatives & Comparisons

1
Linalyl acetate CAS 115-95-7

More lavender-like character with similar volatility, preferred for more traditional floral compositions.

2
Citronellyl acetate CAS 150-84-5

Stronger rosy character, useful when more pronounced floralcy 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. No usage limits established.

RIFM Assessment

Not yet evaluated by RIFM. Limited toxicological data available.

Sustainability

As a synthetic material, production is not dependent on natural resources. Typical synthesis routes use petrochemical feedstocks. Environmental impact depends on manufacturing processes and waste management. No known ecological toxicity at usage levels.

Explore 3,7-Dimethyloct-6-enyl acetate

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

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

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

Report a data error

Similar Posts