l-.alpha.-Pinene (CAS 7785-26-4) — Woody Top Note Fragrance Ingredient

Woody · Green

l-.alpha.-Pinene

CAS 7785-26-4

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

What Is l-.alpha.-Pinene?

α-Pinene is a natural compound found in pine trees and many other plants. It’s what gives pine forests their fresh, resinous scent. You encounter it in cleaning products, air fresheners, and some perfumes. This ingredient matters because it’s one of the most common terpenes in nature, contributing to both fragrance and potential therapeutic effects.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Widely used in consumer products
May cause mild irritation at high concentrations
CAS
7785-26-4
Formula
Mixture
MW
Variable
Odor Family
Woody · Green
Layer 1 · Enthusiast

What Does l-.alpha.-Pinene Smell Like?

α-Pinene smells like walking through a sun-warmed pine forest – crisp, clean, and slightly sharp with a woody-green character. The top note is bright and camphoraceous, evolving into a drier, more resinous heart. In drydown, it leaves a subtle woody trail that blends well with other forest notes.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Pino Silvestre(Vidal, 1955)

Uses α-pinene to create its iconic pine forest accord, giving the fragrance its fresh, masculine opening.

Scent of Peace(Bond No. 9, 2013)

Incorporates α-pinene for its green, uplifting top notes that complement the fruity-floral heart.

Layer 2

2D Molecular Structure

(-)-alpha-Pinene

SMILES: CC1=CC[C@H]2C[C@@H]1C2(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

α-Pinene is a bicyclic monoterpene with the formula C₁₀H₁₆. It exists in two enantiomers: (+)-α-pinene from pine trees and (-)-α-pinene from turpentine. Industrially produced via fractional distillation of turpentine oil or synthesized from β-pinene. The molecule’s strained ring structure makes it reactive in air oxidation.

Physical & Chemical Properties

Boiling Point155-156 °C
Density0.858 g/cm³
Refractive Index1.465

Perfumer Guide

Note Position
Top
Volatility
High (30-90 min)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Fresh top notes
Functional Fragrance5-15%Up to 25%Cleaning products

Classic Accords

+ Cedarwood + Vetiver = Forest + Citrus + Juniper = Gin

Tip: Use to add natural, outdoorsy freshness to masculine and unisex fragrances.

Alternatives & Comparisons

1
β-Pinene CAS 127-91-3

Similar but with a warmer, less sharp character – good when you want softer pine notes.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No restrictions under IFRA standards.

RIFM Assessment

Considered safe as used in fragrance by RIFM.

Sustainability

Most α-pinene is sourced as a byproduct of paper production from pine trees, making it relatively sustainable. Synthetic production exists but is less common. The compound is biodegradable and doesn’t persist in the environment.

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References

  1. PubChem: α-Pinene CID 6654

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

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Physicochemical Properties

DTXSID: DTXSID2029290

Physical Properties

Molecular Weight 136.238 g/mol🔬 EPA CompTox
Density 0.001 g/cm^3🔬 EPA CTX
Boiling Point 154.957 °C🔬 EPA CTX
Melting Point -61.5 °C🔬 EPA CTX
Flash Point 31.15 °C🔬 EPA CTX
Refractive Index 1.479 Dimensionless📊 OPERA
Molar Volume 154.905 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 10226.322 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 4.484 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.484 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.44 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0.135 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 4.86 mmHg🔬 EPA CTX
Viscosity 1.679 cP📊 OPERA
Surface Tension 27.057 dyn/cm📊 OPERA
Thermal Conductivity 114.426 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 0 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 0 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 43.964 cm^3/mol📊 OPERA
Polarizability 17.429 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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