Methyl anthranilate (CAS N° 134-20-3)​

Photo credits: ScenTree SAS

Floral > Orange Blossom > Anthranilic

Methyl anthranilate

Methyl 2-aminobenzoate ; Aminomethyl benzoate ; Carbomethoxyaniline ; 2-(methoxycarbonyl) aniline ; Methyl aminobenzoate ; Nevoli oil

Methyl anthranilate (CAS N° 134-20-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
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Anthranilate de Methyle - 30 Gr - Visit website Je me procure cet ingrédient - - - - - -

Anthranilate de Methyle - 30 Gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 134-20-3

  • EINECS number : 205-132-4

  • FEMA number : 2682

  • FLAVIS number : 09.715

  • JECFA number : 1534

  • Appearance : Colorless liquid to solid

  • Density : ‎1,166

  • Volatility : Heart

  • Price Range :

Physico-chemical properties

  • Molecular formula : C8H9NO2

  • Molecular Weight : 151,16 g/mol

  • Log P : 1,66

  • Fusion Point : 24°C

  • Boiling Point : 255°C

  • Detection Threshold : 0,12 ng/l air

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 123°C

Utilisation

Uses

Uses in perfumery :

Methyl Anthranilate is used for wild strawberry and wild fruit notes, in orange blossom and exotic flower accords: gardenia, tuberose, jasmine.

Year of discovery :

1898

Natural availability :

Methyl Anthranilate is present in Grandiflorum Jasmine Absolute, Neroli EO, Ylang-Ylang Extra EO (and other ylang fractions), Champaca Absolute, in grapes and citrus fruits, from which it can be extracted in its natural state.

Isomerism :

Methyl Anthranilate does not have any isomer used in perfumery.

Synthesis precursor :

Methyl Anthranilate has the ability to easily react with aldehydes to form molecules called Schiff bases, which can serve as a perfumery ingredient or base for a Maillard reaction. For example, Aurantiol (Schiff Base) results from the reaction of this molecule with Hydroxycitronellal and is a raw material also used in perfumery. The Schiff base with Lilial® (Verdantiol) or the one with Triplal® (Vertosine) are also much used.

Synthesis route :

Methyl Anthranilate is synthesized either by esterification of anthranilic acid with methanol or by reaction between methanol and isatoic anhydride, releasing CO2.

Utilisation

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51th :

This ingredient is not restricted for the 51th amendment

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