Vanillin

Aroma chemical · Gourmand / Amber

vanilla, sweet, creamy — base note.

Aroma illustration for Vanillin: vanilla pods and a vanilla orchid, for its vanilla note. It illustrates smell associations, not the material or its source.Skeletal formula of Vanillin, C8H8O3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Vanillin smells like (vanilla), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 1183). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Vanillin is the main odour molecule of vanilla, produced on a large scale by synthesis and also from natural sources. It is one of the most important sweet materials in perfumery.

What Vanillin smells like

Vanillin is the principal odorant of the vanilla pod: sweet, creamy vanilla with a woody, phenolic, slightly smoky edge. Perfumery glossaries contrast it with ethyl vanillin, which reads as vanilla ice cream where vanillin reads as vanilla pod, with less of vanillin's woody, phenolic resin. One source calls it the most consumed aroma chemical in perfumery by volume, used to round out woody-amber and powdery accords as well as gourmands. It discolours many bases.

Leading note
Vanilla pod
Clear facets
Creamy
Supporting facets
Woody, phenolic
Faint facets
Smoky
Character
Sweet, warm, rounded, tenacious
  • vanilla
  • sweet
  • creamy

What makes Vanillin distinctive

Vanilla with its woody, phenolic backbone intact — the pod rather than the dessert.

How Vanillin is used

Used across perfumery: in gourmand and oriental accords, to round off woody-amber and powdery bases, and in vanilla flavours. Its tendency to discolour limits it in some products.

Typical role: backbone (used in large proportions as a structural material of an accord); fixative (slow to evaporate; helps a blend last and holds lighter notes).

How Vanillin differs from similar materials

Ethyl Vanillin
Ethyl vanillin is about three times stronger and creamier, more confectionery — vanilla ice cream rather than vanilla pod — with less phenolic, woody resin. (compared directly by a cited source)
Vanilla Absolute
The absolute adds tobacco, dried fruit, leather and a boozy, resinous depth that vanillin alone lacks. (compared directly by a cited source)
Vanillin Isobutyrate
Vanillin isobutyrate is smoother, creamier and more buttery, without vanillin's phenolic tones or powderiness. (compared directly by a cited source)
Zingerone
Zingerone is vanillin's spicy cousin — sweet vanilla with cooked ginger and a phenolic edge.
Vanitrope
A patent finds Vanitrope less sweet than vanillin, with a phenolic note; it is spicier and more clove-like. (compared directly by a cited source)

An asterisk marks a difference that a cited source states directly. The others compare the published descriptions of each material. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

A crystalline solid; dissolve before use. It turns brown over time and with light, and discolours white bases such as soap.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Gourmand / Amber
Note position
Base note
Physical form at room temperature
Solid
CAS number
121-33-5
Molecular formula
C8H8O3
Molecular weight
152.15 g/mol
IUPAC name
4-hydroxy-3-methoxybenzaldehyde

The CAS number, formula and molecular weight are taken from PubChem compound 1183, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. Companies notifying the ECHA C&L Inventory classify it (2,387 reports): H319 causes serious eye irritation (83.5% of reports); H317 may cause an allergic skin reaction (14.3% of reports). 42 of the reports find it does not meet the hazard criteria. A skin sensitiser classification concerns handling the neat material and the dose in a finished product; the IFRA Standards, where they apply, set the limits. Unless it is harmonised, this is the notifiers' own classification, not a binding one.

This page is general information, not a safety assessment or a specification. Confirm identity, composition, IFRA status and allergen content from your supplier's documents for the lot you hold.

Materials it works with

Vanillin is also suggested as a partner on the pages for 2-Ethylpyrazine, 5-Methyl-2-phenyl-2-hexenal, alpha-Methylcinnamaldehyde, Amber Core, Ambranum and Bran Absolute.

Used in formulas and accords

Used in 74 published formulas

Vanillin is an ingredient in 38 perfume formulas, 34 accords and 2 bases in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Vanillin

Is Vanillin natural or synthetic?

The molecule occurs in nature. Commercial Vanillin may be made by synthesis or obtained from natural sources, so check the supplier's specification if the distinction matters to you.

What is the CAS number of Vanillin?

121-33-5. It was checked against PubChem on 19 October 2026.

Which published formulas use Vanillin?

Vanillin is used in 74 published formulas in the RUŌOD Lab Formula & Accord Library, including Açaí Accord, Amber Accord and Banana Bread. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

Keep your own record of Vanillin — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.