Dimethyl adipate (CAS 627-93-0) — Sweet Base Note Fragrance Ingredient

Sweet · Green

Dimethyl adipate

CAS 627-93-0

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

What Is Dimethyl adipate?

Dimethyl adipate is a synthetic ester commonly used as a solvent and fragrance ingredient in personal care products. It’s found in perfumes, lotions, and other cosmetic formulations where it helps blend other fragrance components. While not a dominant scent itself, it plays a crucial role in stabilizing volatile top notes and extending the longevity of floral and fruity accords in modern perfumery.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Approved for cosmetic use
Low skin irritation potential
CAS
627-93-0
Formula
Mixture
MW
Variable
Odor Family
Sweet · Green
Layer 1 · Enthusiast

What Does Dimethyl adipate Smell Like?

Dimethyl adipate presents a faint, clean ester-like character with subtle fruity undertones reminiscent of green apples or unripe pears. Its odor is neutral-to-sweet, serving primarily as a transparent bridge between brighter top notes and deeper heart accords. The molecule lacks strong olfactory impact but contributes diffusion and lift to fragrance compositions, evaporating cleanly without leaving residual harshness. In dilution, it can impart a barely perceptible waxy-fresh nuance similar to freshly laundered cotton.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Used as a solvent and fixative to enhance the laundry-fresh accord while maintaining transparency.

Glossier You(Glossier, 2017)

Helps balance the musk-ambrette base with its neutral ester character.

Aventus(Creed, 2010)

Contributes to the fruity-pineapple top note diffusion without adding weight.

Layer 2

2D Molecular Structure

Dimethyl adipate

SMILES: COC(=O)CCCCC(=O)OC

Chemistry, Properties & Perfumer Guide

The Chemistry

Dimethyl adipate is a diester formed from adipic acid and methanol. As a linear aliphatic ester, it belongs to the same chemical family as many fruit esters but with higher molecular weight for reduced volatility. Industrial production typically involves direct esterification of adipic acid with methanol under acidic catalysis. The molecule lacks chirality due to its symmetrical structure, making synthetic production straightforward without stereochemical considerations.

Physical & Chemical Properties

AppearanceColorless liquid
Boiling Point215-220 °C
Density1.06 g/cm³
Flash Point107 °C

Perfumer Guide

Note Position
Base
Volatility
Low (hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Fixative/solvent
Personal Care0.5-3%Up to 5%Emollient carrier

Classic Accords

+ Iso E Super = Diffusion booster + Galaxolide = Musk solvent

Tip: Use to solubilize crystalline materials like coumarin without adding significant odor.

Alternatives & Comparisons

1
Diethyl adipate CAS 141-28-6

Higher-boiling alternative with slightly fruitier character.

2
Dimethyl succinate CAS 106-65-0

Shorter-chain ester for brighter compositions.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards.

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

As a petroleum-derived ester, dimethyl adipate’s environmental impact stems from its synthetic origin. However, its high efficiency and low usage levels mitigate footprint concerns. Some manufacturers are exploring bio-based routes using fermented adipic acid precursors to improve sustainability profiles.

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References

  1. PubChem Compound Summary for Dimethyl adipate PubChem
  2. IFRA Standards Library IFRA

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

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Ingredient Data Sheet

CAS 627-93-0

Physical Properties

Molecular Weight174.19 g/mol🔬 PubChem
LogP (Octanol-Water)1🔬 PubChem
Boiling Point109 °C🔬 EPA CompTox
Vapor Pressure0.019 mmHg @ 25°C📊 OPERA
Flash Point107.2 °C🔬 EPA CompTox
Involatility Index0.0015💻 Calculated
log Kp (skin permeability)-3.053💻 Calculated
SMILESCOC(=O)CCCCC(=O)OC🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score2.3 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfruitysweet• leffingwell
Functional Groupsesterether💻 RDKit
“2.5-Dimethyl-2,5-hexanediol Faint, camphorlike odor. This material has been used as a solvent in CH3 fH3 certain fragrance types, but the author be- I lieves that the use of subject material is cH3–c–cH~–cH~–c –cH3 practically abandoned in perfumery and &H AH flavors. It Powerful and, when undiluted, pungent, finds a little use in the construction of arti- sweet-fatty-oily odor, in dilution more p”📖 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: DTXSID8025096

Physical Properties

Molecular Weight 174.196 g/mol🔬 EPA CompTox
Density 1.062 g/cm^3🔬 EPA CTX
Boiling Point 230.9 °C🔬 EPA CTX
Melting Point 8.764 °C🔬 EPA CTX
Flash Point 109.963 °C🔬 EPA CTX
Refractive Index 1.423 Dimensionless📊 OPERA
Molar Volume 167.554 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.064 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 1.094 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.094 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.74 Log10 unitless📊 OPERA
Water Solubility 0.027 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.033 mmHg🔬 EPA CTX
Viscosity 1.384 cP📊 OPERA
Surface Tension 31.965 dyn/cm📊 OPERA
Thermal Conductivity 144.399 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 52.6 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 4 count💻 Computed
Rotatable Bonds 5 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 42.662 cm^3/mol📊 OPERA
Polarizability 16.912 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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