Isopropylquinoline (CAS 1333-53-5) — Woody Base Note Fragrance Ingredient

Woody · Musky

Isopropylquinoline

CAS 1333-53-5

Origin
synthetic
Note
Base
IFRA
Use with awareness
Data as of: Apr 2026

What Is Isopropylquinoline?

Isopropylquinoline is a synthetic aroma chemical used to add leathery, smoky nuances to fragrances. You’ll encounter it in niche perfumes and masculine colognes. This ingredient matters because it creates sophisticated, animalic accords that mimic high-end leather goods and tobacco without using actual animal-derived materials.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Safe in regulated concentrations
Potential sensitizer – check IFRA guidelines
CAS
1333-53-5
Formula
Mixture
MW
Variable
Odor Family
Woody · Musky
Layer 1 · Enthusiast

What Does Isopropylquinoline Smell Like?

Isopropylquinoline delivers an intense leathery-smoky character with earthy undertones. Imagine the inside of a luxury car interior combined with fine cigar tobacco. The scent evolves from sharp, almost rubber-like top notes to a warm, slightly medicinal dry-down that lingers close to the skin for hours. At high concentrations, it can exhibit a phenolic quality reminiscent of antique wood polish.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cuir de Russie(Chanel, 1927)

Used to recreate the classic Russian leather accord, contributing smoky depth alongside birch tar and cade oil in this historic Chanel masterpiece.

Tuscan Leather(Tom Ford, 2007)

Provides the foundational leather note that makes this modern classic smell like expensive Italian car upholstery and raspberry-infused suede.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Isopropylquinoline belongs to the quinoline family of heterocyclic compounds. While quinolines occur naturally in coal tar and some essential oils, the isopropyl derivative is exclusively synthetic. It’s typically produced through Skraup synthesis or by alkylation of quinoline. The isopropyl group at the 2-position creates steric hindrance that modifies both volatility and odor characteristics compared to simpler quinolines.

Physical & Chemical Properties

AppearancePale yellow to brown liquid
Boiling PointApprox. 280-290°C
Density~1.05 g/cm³

Perfumer Guide

Note Position
Base
Volatility
Low (6+ hours)
Blending
Good with woody notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Leather/tobacco accords
Functional Fragrance0.01-0.1%Up to 0.2%Masculine care products

Classic Accords

Tip: Use with ionones to soften harsh edges in leather compositions.

Alternatives & Comparisons

1
Quinoline CAS 91-22-5

More pungent and less refined, suitable for industrial applications where cost is prioritized over subtlety.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA, but recommended maximum 0.1% in leave-on products due to sensitization potential.

GHS Classification

H315 Causes skin irritation H319 Causes serious eye irritation

RIFM Assessment

RIFM has evaluated related quinolines but no specific assessment found for isopropylquinoline.

Sustainability

As a synthetic material, isopropylquinoline has minimal environmental impact during use. Production typically involves petrochemical feedstocks, though modern synthesis routes are optimizing atom economy. Being highly potent, very small quantities are needed, reducing overall resource consumption.

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References

  1. Arctander, S. (1969). Perfume and Flavor Chemicals. Montclair, NJ.

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

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Perfumer’s Notes

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