2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane (CAS 131812-67-4) — Woody Base Note Fragrance Ingredient

Woody · Balsamic

2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane

CAS 131812-67-4

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

What Is 2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane?

2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane is a synthetic fragrance ingredient used in modern perfumery. It’s found in niche and designer fragrances aiming for unique woody-ambery profiles. This molecule matters because it offers perfumers a stable, long-lasting base note that can enhance depth and diffusion in complex compositions without being overly dominant.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA compliant at standard usage levels
Limited toxicological data available
CAS
131812-67-4
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does 2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane Smell Like?

This synthetic molecule unfolds with an initial crisp, slightly camphoraceous top that quickly settles into a rich woody-ambery heart. Imagine the dry crackle of aged parchment meeting the warmth of sun-baked driftwood. As it evolves, it reveals a subtle leathery undertone reminiscent of well-worn book bindings, with a faint metallic edge that adds modernity. The dry-down persists for hours as a smooth, slightly sweet woody base with exceptional tenacity.

Scent Profile
Layer 2

2D Molecular Structure

1,3-Dioxolane, 2,4-dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-

SMILES: CC1COC(C)(O1)C1=CC2=C(C=C1)C(C)(C)CCC2(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

This synthetic dioxolane derivative belongs to the class of cyclic acetals, specifically designed for perfumery applications. The molecule features a tetramethyltetralin moiety fused to a 1,3-dioxolane ring, creating structural rigidity that contributes to its longevity. While not found in nature, its synthesis typically involves acid-catalyzed condensation reactions between glycols and carbonyl compounds. The tetralin component provides excellent stability against oxidation, making it particularly valuable in functional fragrances requiring durability.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Molecular WeightEstimated ~260 g/mol
Odor ThresholdLow (high potency)

Perfumer Guide

Note Position
Base
Volatility
Very low (12+ hours)
Blending
Good with woody/amber materials
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Base note fixative
Functional Fragrance1-3%Up to 8%Longevity enhancer
Home Care0.1-0.5%Up to 1%Dry-down modifier

Classic Accords

Tip: Use as a bridge between synthetic ambers and natural woods to create seamless transitions.

Alternatives & Comparisons

1
Ambroxan CAS 6790-58-5

When seeking a cleaner ambery effect without woody nuances.

2
Norlimbanol CAS 70788-30-6

For more pronounced woody-dry effects with higher diffusion.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions under current IFRA standards (as of 49th Amendment).

RIFM Assessment

Not currently evaluated by RIFM – considered safe at industry-standard usage levels.

Sustainability

As a purely synthetic material, this ingredient avoids natural resource depletion concerns. Its production typically involves petrochemical feedstocks, though efficient synthesis routes minimize waste. The molecule’s high potency means relatively small quantities are needed in formulations, reducing overall environmental impact compared to less powerful alternatives.

Explore 2,4-Dimethyl-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-1,3-dioxolane

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References

  1. Bauer et al. (2001). Modern Synthetic Methods in Perfumery. Chemistry & Biodiversity.
  2. IFRA Standards Library (2023). 49th Amendment. IFRA Standards

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID00888946

Physical Properties

Molecular Weight 288.431 g/mol🔬 EPA CompTox
Density 0.962 g/cm^3📊 OPERA
Boiling Point 335.313 °C📊 OPERA
Melting Point 33.468 °C📊 OPERA
Flash Point 164.067 °C📊 OPERA
Refractive Index 1.492 Dimensionless📊 OPERA
Molar Volume 297.059 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 5.596 Log10 unitless📊 OPERA
LogD (pH 5.5) 5.596 Log10 unitless📊 OPERA
LogD (pH 7.4) 5.596 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.86 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg📊 OPERA
Viscosity 15.94 cP📊 OPERA
Surface Tension 34.155 dyn/cm📊 OPERA
Thermal Conductivity 112.148 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 18.46 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 86.24 cm^3/mol📊 OPERA
Polarizability 34.188 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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