Skip to main content

    Ingredient Profile

    Indole fragrance note

    Indole, a nitrogen‑bearing heterocycle, bridges the natural world of jasmine blossoms with the laboratory, delivering a distinctive floral‑g…More

    India

    2

    Fragrances

    Fragrances featuring Indole

    Character

    The Story of Indole

    Indole, a nitrogen‑bearing heterocycle, bridges the natural world of jasmine blossoms with the laboratory, delivering a distinctive floral‑green nuance that anchors many modern perfumes.

    Heritage

    Indole entered the scent world in the late 1800s, when chemists first identified its presence in jasmine and orange blossom extracts. Early analytical work by German researchers linked the compound to the characteristic “heady” note of these flowers. In 1883, the first synthetic batch was produced in a laboratory, but the material remained a curiosity due to low yields. The breakthrough arrived in 1901, when the Fischer indole synthesis was refined to deliver gram‑scale quantities, allowing perfumers to experiment beyond the limits of natural harvests. By the 1920s, indole appeared in iconic creations such as Chanel No 5, where it added depth to the aldehydic bouquet. Throughout the 20th century, the molecule became a staple in floral‑green and animalic accords, prized for its ability to evoke the scent of fresh cut petals while anchoring the composition. Today, indole remains a bridge between nature and chemistry, illustrating how a single heterocycle reshaped modern perfumery.

    At a Glance

    Fragrances

    2

    Feature this note

    Origin

    India

    Primary source region

    Ingredient Details

    Extraction

    Synthetic (Fischer indole synthesis)

    Used Parts

    Jasmine flower petals

    Did You Know

    "A single gram of natural jasmine oil contains roughly 25 mg of indole, yet the compound’s aroma can dominate a perfume’s character at concentrations as low as 0.1 %."

    Production

    How Indole Is Made

    Indole reaches the perfume lab through two main routes. Natural jasmine oil, harvested at dawn to preserve volatile compounds, undergoes solvent extraction with hexane; the resulting crude extract is fractionated by low‑temperature vacuum distillation, isolating indole crystals that account for roughly 2.5 % of the oil. The bulk of commercial indole, however, is synthesized. The classic Fischer indole synthesis combines phenylhydrazine with a suitable ketone under acidic conditions, forming the heterocycle in a single step. After reaction, the mixture is cooled, and indole precipitates as white needles. Recrystallization from ethanol removes impurities, yielding a product of 99 % purity. Modern plants scale the reaction in stainless‑steel reactors, recycle solvents, and employ automated crystallizers to meet fragrance‑industry demand while minimizing waste.

    Provenance

    India

    India13.0°N, 77.6°E

    About Indole