Aurantiol

Aroma chemical · Floral / Powdery

orange blossom, honeyed, floral, heavy — base note.

Aroma illustration for Aurantiol: white orange blossoms and honeycomb and a drop of honey, for its orange blossom and honeyed notes. It illustrates smell associations, not the material or its source.Skeletal formula of Aurantiol (Aurantia), C18H27NO3, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Aurantiol smells like (orange blossom, honeyed), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 98118). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Aurantiol is the Schiff base formed from hydroxycitronellal and methyl anthranilate. It gives a heavy, sweet orange-blossom note with great tenacity.

What Aurantiol smells like

Aurantiol, the Schiff base of methyl anthranilate and hydroxycitronellal, is a floral-balsamic, sweet orange-blossom material. A 2018 study found its synthesised product floral-balsamic, sweet and orange-blossom-like; a supplier lists floral-orange blossom, slightly sweet, powdery and faintly balsamic. A glossary adds honeyed warmth and a slightly animalic undertone, describing it as sweeter and deeper than neroli and less indolic than orange-flower absolute. Like other Schiff bases it is more stable and longer-lasting than its parent aldehyde. Fraterworks, which lists Aurantia and Auralva as synonyms, describes an intensely sweet, heavy floral dominated by orange blossom and neroli, with grape-like nuances and subtle powdery, balsamic undertones — the scent of orange flowers and honey — in an intensely yellow, very viscous liquid.

Leading note
Sweet orange blossom
Clear facets
Honeyed
Supporting facets
Balsamic, powdery
Faint facets
Linden
Character
Heavy, sweet, warm, tenacious
  • orange blossom
  • honeyed
  • floral
  • heavy

What makes Aurantiol distinctive

It is a long-lasting, honeyed orange blossom — sweeter and deeper than neroli, softer than the absolute, and a fixative as much as a floral.

Where the descriptions disagree: Sources disagree on its regulatory position. The IFRA Standards Library snapshot names no Standard for Aurantiol itself, only for hydroxycitronellal, from which it is made; Scentree says no IFRA Standard applies; Fraterworks gives a category limit; a glossary calls it restricted for the sensitisation potential of Schiff bases. Scentree lists the hazard statements H317 and H319. Its appearance is given as a viscous liquid by Fraterworks and Scentree and as a waxy solid by one glossary.

How Aurantiol is used

Used in orange-blossom, neroli and white-floral compositions and in citrus colognes, both as a fixative and to enhance the top note. Scentree notes it is unstable in acidic products (fabric conditioners excepted) and in alkaline detergents other than soap.

Typical role: fixative (slow to evaporate; helps a blend last and holds lighter notes).

How Aurantiol differs from similar materials

Methyl Anthranilate
Methyl anthranilate is grapier and more volatile; aurantiol, made from it, is sweeter, deeper, more balsamic and far longer-lasting.
Neroli Oil
A glossary describes aurantiol as sweeter and deeper than neroli; neroli is fresher, greener and more citrus. (compared directly by a cited source)
Orange Flower Absolute
A glossary describes aurantiol as less indolic than orange-flower absolute; the absolute is richer and more animalic. (compared directly by a cited source)
Indolene
Indolene, the hydroxycitronellal–indole condensation product, is more indolic and jasmine-like, with a mothball edge; Aurantiol is sweeter and honeyed, pure orange blossom.

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

Very viscous and yellow-orange; it colours a formula. Schiff bases can slowly revert in some media.

Identity and classification

Type
Aroma chemical
Origin
Synthetic
Odour family
Floral / Powdery
Note position
Base note
Physical form at room temperature
Viscous liquid
Also known as
Hydroxycitronellal methyl anthranilate Schiff base, Aurantia
CAS number
89-43-0
Molecular formula
C18H27NO3
Molecular weight
305.4 g/mol
IUPAC name
methyl 2-[(7-hydroxy-3,7-dimethyloctylidene)amino]benzoate

The CAS number, formula and molecular weight are taken from PubChem compound 98118, 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 (1,606 reports): H317 may cause an allergic skin reaction (80.7% of reports); H319 causes serious eye irritation (80.7% of reports). 310 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

Aurantiol is also suggested as a partner on the pages for Nerolin Bromelia.

Used in formulas and accords

Used in 7 published formulas

Aurantiol is an ingredient in 3 perfume formulas, 2 accords and 2 bases in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Aurantiol

Is Aurantiol natural or synthetic?

Aurantiol is synthetic — it is made by chemical synthesis.

What is the CAS number of Aurantiol?

89-43-0. It was checked against PubChem on 19 October 2026.

Which published formulas use Aurantiol?

Aurantiol is used in 7 published formulas in the RUŌOD Lab Formula & Accord Library, including Honeysuckle Base, Mandarin Tiles and Neroli Bigarade Base. 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 Aurantiol — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.