Geranyl tiglate (CAS 7785-33-3) — Floral Middle Note Fragrance Ingredient

Floral · Sweet

Geranyl tiglate

CAS 7785-33-3

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

What Is Geranyl tiglate?

Geranyl tiglate is a synthetic fragrance ingredient used in perfumes and personal care products. It’s valued for its fresh, floral, and slightly fruity aroma. This ester compound helps create natural-smelling floral bouquets and adds complexity to fragrance compositions.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns
Patch test recommended for sensitive skin
CAS
7785-33-3
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Geranyl tiglate Smell Like?

Geranyl tiglate opens with a bright, fresh floral character reminiscent of rose petals and lily of the valley. The heart reveals a juicy, slightly tropical fruitiness akin to ripe passionfruit, while the dry-down carries a soft, powdery muskiness. The tiglate moiety adds a subtle animalic depth that prevents the floral aspects from becoming too sweet or cloying. It behaves like a natural floral absolute but with superior stability in formulations.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used as a modern floralizer to enhance the abstract floral bouquet, providing lift to the aldehydic top notes while blending seamlessly with the ylang-ylang and rose heart.

Dior J'adore(Christian Dior, 1999)

Contributes to the luminous floralcy, bridging between the fresh pear top notes and the rich damask rose heart with its dual fruity-floral character.

Layer 2

2D Molecular Structure

Geranyl tiglate

SMILES: C\C=C(/C)C(=O)OC\C=C(/C)CCC=C(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Geranyl tiglate is an ester formed from geraniol and tiglic acid. As a synthetic material, it’s typically produced via acid-catalyzed esterification. The molecule features both a terpene alcohol moiety (geraniol) and an unsaturated carboxylic acid (tiglic acid), giving it unique stability and odor properties. The trans configuration of the tiglate double bond contributes to its clean floral character without excessive sweetness.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor StrengthMedium to strong

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Floral bouquet enhancer
Soap0.1-0.5%Up to 1%Adds floral persistence

Classic Accords

+ Rose Oxide + Hedione = Modern Rose + Galaxolide + Ethyl Linalool = Clean Floral

Tip: Use to add natural floralcy to rose and white flower reconstructions without introducing excessive sweetness.

Alternatives & Comparisons

1
Geranyl acetate CAS 105-87-3

More citrusy and less floral, suitable when a brighter top note is needed but lacks the fruity depth of the tiglate ester.

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 (as of 49th Amendment).

RIFM Assessment

Considered safe for current fragrance use levels based on RIFM evaluation.

Sustainability

As a synthetic material, geranyl tiglate offers consistent quality without natural sourcing constraints. Production can utilize renewable carbon sources. Its stability reduces need for frequent reapplication in products, contributing to lower overall environmental impact compared to some natural alternatives.

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References

  1. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

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

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Physicochemical Properties

DTXSID: DTXSID9047413

Physical Properties

Molecular Weight 236.355 g/mol🔬 EPA CompTox
Density 0.907 g/cm^3📊 OPERA
Boiling Point 296.415 °C📊 OPERA
Melting Point 11.392 °C📊 OPERA
Flash Point 152.8 °C🔬 EPA CTX
Refractive Index 1.474 Dimensionless📊 OPERA
Molar Volume 259.867 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.856 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.856 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.856 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 7.43 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.004 mmHg📊 OPERA
Surface Tension 27.529 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 6 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 73.018 cm^3/mol📊 OPERA
Polarizability 28.947 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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