gamma-Methyldecalactone (CAS 7011-83-8) — Sweet Base to Middle Note Fragrance Ingredient

Sweet · Floral

gamma-Methyldecalactone

CAS 7011-83-8

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

What Is gamma-Methyldecalactone?

Gamma-Methyldecalactone is a synthetic musk-like ingredient used in perfumes and body care products. It creates creamy, fruity, and slightly woody undertones that enhance luxury fragrances. This lactone is prized for its ability to add depth and persistence to floral and fruity compositions, making scents feel more expensive and sophisticated.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
IFRA-approved for fragrance use
Avoid direct skin application in high concentrations
CAS
7011-83-8
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does gamma-Methyldecalactone Smell Like?

Gamma-Methyldecalactone unfolds with an initial burst of creamy peach skin and coconut flesh, evolving into a velvety musk with hints of sun-warmed sandalwood. Its dry-down reveals a sophisticated skin-like quality – imagine cashmere soaked in apricot nectar. The molecule behaves like an olfactory chameleon, amplifying fruity notes in top notes while anchoring florals with its persistent lactonic warmth.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Baccarat Rouge 540(Maison Francis Kurkdjian, 2015)

Provides the signature ambery-saffron illusion through its lactonic muskiness, blending with jasmine to create the fragrance’s addictive, skin-hugging trail.

Angel(Mugler, 1992)

Accentuates the gourmand patchouli with creamy fruit nuances, helping bridge the gap between sharp bergamot and rich chocolate notes.

Layer 2

2D Molecular Structure

Dihydrojasmone lactone

SMILES: CCCCCCC1(C)CCC(=O)O1

Chemistry, Properties & Perfumer Guide

The Chemistry

Gamma-Methyldecalactone belongs to the macrocyclic lactone family, structurally featuring a ten-membered ring with a methyl group at the gamma position. While found trace amounts in some fruits, commercial production typically involves ring-closing metathesis of decenoic acid derivatives or Baeyer-Villiger oxidation of corresponding ketones. The gamma-methyl substitution creates unique steric hindrance that modulates its odor profile compared to straight-chain decalactones.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~280 °C (estimated)
Density~0.95 g/cm³ (estimated)

Perfumer Guide

Note Position
Base to Middle
Volatility
Low (8+ hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance0.5-3%Up to 5%Musk enhancer in oriental compositions
Body Care0.1-1%Up to 2%Skin-smoothing effect in lotions

Classic Accords

Tip: Use to round off sharp aldehyde notes while maintaining projection in floral bouquets.

Alternatives & Comparisons

1
Ethylene Brassylate CAS 105-95-3

When cleaner musk effect is needed without fruity undertones.

2
Pantolactone CAS 599-04-2

For brighter lactonic effects in citrus colognes.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No restrictions under IFRA 49th Amendment. Classified as safe for use in all fragrance categories.

RIFM Assessment

RIFM evaluation confirms safe use at current industry levels with wide margin of safety.

Sustainability

Synthetic production avoids agricultural land use. Major manufacturers employ green chemistry principles including catalytic processes with >90% atom economy. Biodegradation studies show complete breakdown within 28 days under OECD 301 conditions.

Explore gamma-Methyldecalactone

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. Brenna E et al. (2002). Stereoisomeric flavor compounds. Chemical Reviews. DOI:10.1021/cr010086j

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

Report a data error

Ingredient Data Sheet

CAS 7011-83-8

Physical Properties

Molecular Weight184.27 g/mol🔬 PubChem
LogP (Octanol-Water)3.3🔬 PubChem
Boiling Point135 °C🔬 EPA CompTox
Vapor Pressure0.36 mmHg @ 25°C📊 OPERA
Flash Point144 °C🔬 EPA CompTox
Involatility Index0.0286💻 Calculated
log Kp (skin permeability)-1.481💻 Calculated
SMILESCCCCCCC1(CCC(=O)O1)C🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassSlow💻 Calculated
Persistence Score0.8 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsjasminepeachwaxy• leffingwell
Functional Groupsesterether💻 RDKit
“B: I and waxy odor. 201” C, room spray fragrances, etc. There is consider- Refreshing herbaceous-minty, also Pulegol- able difference in odor between the materials like, Lavender type odor of moderate tenacity.”📖 Arctander
g-Methyldecalactone has a jasmine-like odor.📖 Fenaroli
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: DTXSID3041299

Physical Properties

Molecular Weight 184.279 g/mol🔬 EPA CompTox
Density 0.942 g/cm^3🔬 EPA CTX
Boiling Point 285 °C🔬 EPA CTX
Melting Point -14.2 °C🔬 EPA CTX
Flash Point 144 °C🔬 EPA CTX
Refractive Index 1.444 Dimensionless📊 OPERA
Molar Volume 198.278 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.313 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.313 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.313 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.36 Log10 unitless📊 OPERA
Water Solubility 0.002 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.405 mmHg🔬 EPA CTX
Viscosity 2.707 cP📊 OPERA
Surface Tension 29.691 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 26.3 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 5 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 52.654 cm^3/mol📊 OPERA
Polarizability 20.874 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.

Similar Posts