1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl- (CAS 60899-29-8) — Woody Middle to base Note Fragrance Ingredient

Woody · Balsamic

1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl-

CAS 60899-29-8

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

What Is 1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl-?

1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl- is a synthetic fragrance ingredient primarily used in industrial and niche perfumery. It’s not commonly encountered in everyday consumer products but may appear in avant-garde or experimental fragrances. This compound contributes unique woody and amber nuances, valued for its ability to add complexity and depth to fragrance compositions where traditional ingredients fall short.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for fragrance use
Limited safety data available
CAS
60899-29-8
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does 1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl- Smell Like?

This synthetic molecule offers a bold, unconventional olfactory profile. Initially presents with sharp, almost metallic woody tones that quickly evolve into a warm, resinous heart reminiscent of aged amber and fossilized resins. The dry-down reveals subtle leathery undertones with a faintly animalic edge, behaving like a chameleon that shifts between modern synthetic crispness and ancient amber warmth. Lasting power is moderate with a tendency to cling to fabric fibers.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

1H-Indene, 1-ethyl-2,3-dihydro-1,3,3-trimethyl- belongs to the indane chemical class, characterized by a fused benzene and cyclopentane ring system. The ethyl and methyl substitutions create steric hindrance that influences its volatility and odor characteristics. Synthesized through Friedel-Crafts alkylation reactions, this compound exemplifies how subtle modifications to indane structures can dramatically alter olfactory properties. The absence of chirality simplifies production but limits olfactory nuance compared to asymmetric analogs.

Physical & Chemical Properties

Perfumer Guide

Note Position
Middle to base
Volatility
Moderate (2-6 hours)
Blending
Specialized
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used as an amber modifier
Functional Fragrance0.1-0.5%Up to 1%For industrial applications

Classic Accords

Tip: Use sparingly as an amber enhancer in woody-oriental bases where traditional materials need modern augmentation.

Alternatives & Comparisons

1
1,1,2,3,3-Pentamethyl-2,3-dihydro-1H-inden-5-yl acetate CAS 68039-57-2

Offers similar woody-indole character with added floralcy from the acetate group, useful when more diffusion is needed.

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

No RIFM assessment available; treat as precautionary material.

Sustainability

As a fully synthetic material, this compound avoids natural resource depletion but requires petrochemical feedstocks. Production energy costs are moderate compared to complex natural isolates. Being a single molecule simplifies biodegradability prediction compared to complex natural mixtures.

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References

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

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