1,3-Dioxolane-4-methanol, 2,2-dimethyl (CAS 100-79-8) — Citrus N/A Note Fragrance Ingredient

Citrus · Floral

1,3-Dioxolane-4-methanol, 2,2-dimethyl

CAS 100-79-8

Origin
synthetic
Note
N/A
IFRA
Professional use
Data as of: Apr 2026

What Is 1,3-Dioxolane-4-methanol, 2,2-dimethyl?

1,3-Dioxolane-4-methanol, 2,2-dimethyl is a synthetic compound primarily encountered in industrial applications and specialized chemical formulations. While not commonly used in consumer products, it may appear in certain niche fragrances or functional materials. Its significance lies in its potential as a versatile chemical intermediate, though its direct consumer applications are limited.

Safety Profile

PROFESSIONAL USE
Generally safeUse with awarenessProfessional use
Handle with care – industrial chemical
Limited safety data available
CAS
100-79-8
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does 1,3-Dioxolane-4-methanol, 2,2-dimethyl Smell Like?

This synthetic compound lacks a distinctive odor profile, as it is primarily valued for its chemical properties rather than its olfactory characteristics. In industrial contexts, it may exhibit faint solvent-like notes, but these are not typically leveraged in perfumery.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Layer 2

2D Molecular Structure

Solketal

SMILES: CC1(C)OCC(CO)O1

Chemistry, Properties & Perfumer Guide

The Chemistry

1,3-Dioxolane-4-methanol, 2,2-dimethyl is a synthetic organic compound belonging to the dioxolane family. It is primarily used as an intermediate in chemical synthesis. The compound features a dioxolane ring with a methanol substituent, making it a versatile building block for more complex molecules. Its synthesis typically involves the reaction of appropriate glycols with aldehydes or ketones under acidic conditions.

Physical & Chemical Properties

Boiling PointN/A
DensityN/A

Perfumer Guide

Note Position
N/A
Volatility
N/A
Blending
N/A
ApplicationTypical %RangeNotes
IndustrialN/AN/APrimarily used as a chemical intermediate

Classic Accords

Tip: Not recommended for perfumery use due to lack of olfactory characteristics.

Alternatives & Comparisons

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions listed.

EU Allergen Declaration

Not listed as an EU allergen.

RIFM Assessment

No RIFM safety assessment available.

Sustainability

As a synthetic compound, its environmental impact depends on production methods. No significant sustainability concerns are documented, but standard industrial chemical handling precautions apply.

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References

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

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    Ingredient Data Sheet

    CAS 100-79-8

    Physical Properties

    Molecular Weight132.16 g/mol🔬 PubChem
    LogP (Octanol-Water)-0.2🔬 PubChem
    Boiling Point188.5 °C🔬 EPA CompTox
    Vapor Pressure107 mmHg @ 25°C📊 OPERA
    Flash Point80 °C🔬 EPA CompTox
    Involatility Index10.0314💻 Calculated
    log Kp (skin permeability)-3.648💻 Calculated
    SMILESCC1(OCC(O1)CO)C🔬 PubChem

    Volatility & Performance

    Fragrance NoteTop💻 Calculated
    Volatility ClassVery fast💻 Calculated
    Persistence Score0.5 / 5💻 Calculated

    Odor & Flavor

    Primary Descriptorsfruitysolvent• leffingwell
    Functional Groupsalcoholether💻 RDKit
    “Very diffusive, slightly choking or nauseating, Pear-like odor of very poor tenacity. In aqueous dilution the odor appears very weak”📖 Arctander

    Flavor Notes (Arctander)

    “The taste is sweet, mildly ethereal-fruitly. The subject acetal is mentioned in this work mainly because it is an important parent or prototype of a group of interesting perfume and flavor chemicals, and related to the Dioxanes. The title material is also used as a solvent in the extraction of flavo”📖 Arctander
    Data Sources & Attribution
    Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

    Physicochemical Properties

    DTXSID: DTXSID9021845

    Physical Properties

    Molecular Weight 132.159 g/mol🔬 EPA CompTox
    Density 1.06 g/cm^3🔬 EPA CTX
    Boiling Point 188.5 °C🔬 EPA CTX
    Melting Point -27 °C🔬 EPA CTX
    Flash Point 80 °C🔬 EPA CTX
    Refractive Index 1.424 Dimensionless📊 OPERA
    Molar Volume 127.788 cm^3/mol📊 OPERA

    Partition & Solubility

    LogP (Octanol-Water) -0.6 Log10 unitless🔬 EPA CTX
    LogD (pH 5.5) 0.049 Log10 unitless📊 OPERA
    LogD (pH 7.4) 0.049 Log10 unitless📊 OPERA
    LogKoa (Octanol-Air) 4.91 Log10 unitless📊 OPERA
    Water Solubility 1.3 mol/L🔬 EPA CTX
    Henry's Law Constant 0 atm-m3/mole📊 OPERA

    Transport Properties

    Vapor Pressure 0.638 mmHg🔬 EPA CTX
    Viscosity 9.087 cP📊 OPERA
    Surface Tension 33.42 dyn/cm📊 OPERA
    Thermal Conductivity 145.164 mW/(m*K)📊 OPERA

    Molecular Descriptors

    Topological Polar Surface Area 38.69 Ų💻 Computed
    H-Bond Donors 1 count💻 Computed
    H-Bond Acceptors 3 count💻 Computed
    Rotatable Bonds 1 count💻 Computed
    Aromatic Rings 0 count💻 Computed
    Molar Refractivity 32.596 cm^3/mol📊 OPERA
    Polarizability 12.922 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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