1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)- (CAS 70356-09-01) — Sweet Middle Note Fragrance Ingredient

Sweet · Woody

1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)-

CAS 70356-09-01

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

What Is 1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)-?

This synthetic fragrance ingredient is a specialized chemical compound primarily used in modern perfumery. It’s found in select niche fragrances where unique olfactory effects are desired. While not commonly encountered by consumers directly, it contributes to complex scent profiles in premium products.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for fragrance use
Limited safety data available
CAS
70356-09-01
Formula
Mixture
MW
Variable
Odor Family
Sweet · Woody
Layer 1 · Enthusiast

What Does 1,3-Propanedione, 1-[4-(1,1-dimethylethyl)phenyl]-3-(4-methoxyphenyl)- Smell Like?

This synthetic molecule offers a distinctive aromatic profile with subtle nuances. Initial impressions suggest a delicate balance between soft powderiness and faint woody undertones. As it evolves, there’s a whisper of almond-like character with a clean, almost soapy dry-down. The scent maintains remarkable tenacity while remaining transparent, making it valuable for modern fragrance architectures.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

1,3-Propanedione derivatives represent an important class of fragrance ingredients. This particular compound features a central diketone structure flanked by aromatic substituents – a tert-butylphenyl group and a methoxyphenyl moiety. The electron-donating methoxy group influences the compound’s electronic properties and olfactory characteristics. Synthesis typically involves Friedel-Crafts acylation followed by selective oxidation steps.

Physical & Chemical Properties

Molecular ClassAromatic diketone
Structural FeaturesTert-butyl and methoxy substituents

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 3%Used as subtle modifier
Functional Fragrance0.1-0.5%Up to 1%For sophisticated effects

Classic Accords

Tip: Use sparingly to add dimensionality without dominating compositions.

Alternatives & Comparisons

1
Benzophenone CAS 119-61-9

Offers similar structural features with more established safety profile and rosy-woody character.

2
Damascone CAS 23726-91-2

Provides fruity-woody aspects with greater intensity and diffusion.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions currently apply to this material.

RIFM Assessment

Full safety assessment pending due to limited commercial use history.

Sustainability

As a synthetic material, production can be carefully controlled with minimal environmental impact. The manufacturing process allows for precise quality control and consistent output. Being petroleum-derived, its sustainability depends on the energy sources used in production.

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References

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

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