Methyl Benzoate

Aroma chemical · Floral / Fruity

sweet, floral, fruity, medicinal — top to heart note.

Aroma illustration for Methyl Benzoate: pink flowers and bright abstract fruit-coloured spheres, for its floral and fruity notes. It illustrates smell associations, not the material or its source.Skeletal formula of Methyl Benzoate (Niobe oil), C8H8O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Methyl Benzoate smells like (floral, fruity), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 7150). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

Methyl benzoate is a simple aromatic ester found in tuberose, ylang ylang and feijoa. It has a sweet, fruity-floral odour with a phenolic, medicinal edge.

What Methyl Benzoate smells like

Methyl benzoate is a strong, medicinal-phenolic, sweet-floral material. Symrise describes it as strongly phenolic, close to cresol and wintergreen oil, and sweet-floral like ylang-ylang and tuberose; its taste is medicinal-balsamic and slightly fruity in dilution. Other descriptions add a dry-fruity side, cherry and almond, while one supplier hears fresh green wintergreen, eucalyptus and mint. It occurs naturally in ylang-ylang, tuberose and Michelia. Harsh on its own, it reads as natural inside a white floral.

Leading note
Medicinal sweet floral
Clear facets
Phenolic, wintergreen-like
Supporting facets
Ylang, tuberose
Faint facets
Dry fruity, cherry
Character
Sharp, harsh, sweet, diffusive
  • sweet
  • floral
  • fruity
  • medicinal

What makes Methyl Benzoate distinctive

The medicinal edge of white flowers: the note that gives ylang and tuberose their slightly wintergreen, narcotic sharpness.

Where the descriptions disagree: One supplier describes a fresh green wintergreen-eucalyptus-mint odour rather than a sweet floral.

How Methyl Benzoate is used

Used in traces in white floral accords — ylang, tuberose, narcissus — where it adds natural sharpness; it easily dominates.

Typical role: modifier (used in small amounts to change the character of a blend).

How Methyl Benzoate differs from similar materials

Ylang Ylang Oil
Methyl benzoate is one of ylang-ylang's natural constituents — its medicinal sharpness on its own, without the oil's creamy, banana and clove body. (compared directly by a cited source)
Tuberose Absolute
A perfumer links tuberose's slightly medicinal edge to methyl benzoate and methyl salicylate; the absolute adds creaminess, coconut and indole. (compared directly by a cited source)
Methyl Salicylate
Methyl salicylate is wintergreen itself; methyl benzoate is a sweeter floral with a cresol-wintergreen phenolic side.
Ethyl Benzoate
Ethyl benzoate is fruitier, cherry and grape; methyl benzoate is more floral and phenolic, ylang and tuberose.

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

Powerful in the top; use sparingly.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Floral / Fruity
Note position
Top to heart note
Physical form at room temperature
Liquid
Also known as
Niobe oil
CAS number
93-58-3
Molecular formula
C8H8O2
Molecular weight
136.15 g/mol
IUPAC name
methyl benzoate

The CAS number, formula and molecular weight are taken from PubChem compound 7150, 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 (2,105 reports): H302 harmful if swallowed (99.7% of reports). 7 of the reports find it does not meet the hazard criteria. 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

Methyl Benzoate is also suggested as a partner on the pages for cis-3-Hexenyl Tiglate and Ethyl Benzoate.

Used in formulas and accords

Used in 6 published formulas

Methyl Benzoate is an ingredient in 2 perfume formulas, 3 accords and 1 base in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about Methyl Benzoate

Is Methyl Benzoate natural or synthetic?

The molecule occurs in nature. Commercial Methyl Benzoate 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 Methyl Benzoate?

93-58-3. It was checked against PubChem on 19 October 2026.

Which published formulas use Methyl Benzoate?

Methyl Benzoate is used in 6 published formulas in the RUŌOD Lab Formula & Accord Library, including Gardenia Accord, Gasoline Accord and Honeysuckle 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 Methyl Benzoate — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.