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TETRAHYDRO-PARA-METHYLQUINOLINE

CAS
—
EC
—
Material type
synthetic aroma chemical
Canonical source
arctander
Formulation

Usage guidance

Suggested min
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Suggested max
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Cost
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Stock
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Compatibility tags
leatheranimalicwhite-floralchypreoriental
How it behaves

Olfactory profile

Family
sweet
Note tendency
Base
Descriptors
floralsweethoney

An intensely animalic, fecal-leathery aromachemical with a narcotic floral undertone reminiscent of overripe jasmine and civet. In extreme dilution it lends a warm, skin-like radiance and leather nuance; neat it is repulsively barnyard and horse-stable. Signature use is trace-dosing to add carnal depth to florals and leather accords.AI · claude-opus-4-7

Intensity
9 / 10
Tenacity
9 / 10
Volatility
2 / 10
Members

The rest of this material

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chemicals · No. 2917

Arctander monograph

Perfume and Flavor Chemicals, page 1295.

BASEtenacity · highpower · strong
sweetanimalfloral
MW
147.22
BP
265°C
MP
38°C
Sp.Gr.
—
Refractive n
—
Rotation
—
Appearance

Colorless or pale amber-colored, needle-like crystals.

Solubility

Slightly soluble in water, soluble in alcohol and oils.

Odor

Very powerful and tenacious, sweet-animal odor with honey-like undertone. Floral notes are perceptible upon extreme dilution of the material, but the undiluted quinoline has a rather unpleasant, civet-like odor.

Uses in perfumery

This material is one of the most frequently used quinoline derivatives in perfumery. It is used in artificial civet or civet bases, as a fixative in floral, balsamic, Oriental or Ambre-like fragrances, and in honey or tabac bases. It is almost a standard ingredient, although always in discrete proportions. It also blends well with Amylcinnamic aldehyde for variations in the Jasmin theme, Tuberose, Gardenia and many other heavy or exotic florals. With Phenylacetic acid, Opopanax, Sandalwood and Cinnamates, it may contribute fixation and background for Oriental fragrances.

Production

Produced from 6-Methylquinoline hydrochloride by reduction with nascent hydrogen, followed by neutralization. Also with hydrogen and a nickel catalyst. The methylquinoline is usually obtained by a Skraup’s synthesis.

Identity
Aliases · 7
1,2,3,4-Tetrahydro-6-methylquinolineCivettalpara-Methyl tetrahydroquinolineTetrahydro-para-toluquinoneTetraquinoneZiberthineZibethal
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).