Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | Purity | Latin name | Treated part | Geographical origin | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Anthranilate de Methyle - 30 Gr | - |
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METHYL ANTHRANILATE 10KG DRUM STEEL | 442FP24223 |
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Synthetic Aroma Chemicals |
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- | - | - | India | - |
Anthranilate de Methyle - 30 Gr
Certifications :
METHYL ANTHRANILATE 10KG DRUM STEEL
ID : 442FP24223
India
Certifications :
General Presentation
-
CAS N° :
134-20-3 -
EINECS number :
205-132-4 -
FEMA number :
2682 -
FLAVIS number :
09.715
-
JECFA number :
1534 -
Volatility :
Heart -
Price Range :
€
Physico chemical properties
-
Appearance :
Colorless liquid to solid -
Density :
1,166 -
Refractive Index @20°C :
1,581 – 1,585 -
Optical rotation :
Data not available. -
Vapor pressure :
0,0133 hPa @20°C 0,021 hPa @25°C -
Flash Point :
123°C
-
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
Chemistry & Uses
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.
Stability :
Methyl Anthranilate is well known for synthesizing Schiff bases by reacting espacially with aldehydes. These compounds can have an olfactive interest but are still a source of coloration in perfume concentrates and perfumes besides others. This is why this raw material is used is small quantities.
Exclusively stable in fabric conditioners, shampoos and hair conditioners
Other comments :
Methyl Anthranilate is more associated with Orange Blossom Absolute notes and fruity notes of wild strawberry than Dimethyl Anthranilate, closer to Mandarin Yellow EO.
Regulations & IFRA
Allergens :
This ingredient does not contain any allergen.
IFRA 51th :
This ingredient is not restricted for the 51th amendment
