Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
METHYL BENZOATE | M_0050654 | Naturel | - | - | - | - | more | - |
General Presentation
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CAS N° : : 93-58-3
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EINECS number : 202-259-7
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FEMA number : 2683
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Density : 1,086
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : 09.725
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JECFA number : 851
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 200°C
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Detection Threshold : 110 ppb (0,000011%)
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Molecular formula : C8H8O2
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Log P : 2,2
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Molecular Weight : 136,15 g/mol
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Fusion Point : -15°C
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Flash Point : 77°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Methyl Benzoate has a more neutral smell, but much more powerful than Benzyl Benzoate.
Stability :
Can form benzoic acid through time.
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Methyl Benzoate is used in white floral notes such as ylang-ylang, jasmine, tuberose, mimosa or leather and cinnamic notes.
Year of discovery :
Data not available.
Isomerism :
Phenylacetic Acid and Anisic Aldehyde are constitutional isomers of Methyl Benzoate. Their smell is however very different.
Synthesis precursor :
Methyl Benzoate is a major intermediate in the synthesis of Polyethylene Terephtalate (PET), which is the plastic that we consume every day.
Natural availability :
Methyl Benzoate is especially present in Ylang-Ylang Extra EO (and other ylang fractions), from which it can be extracted in its natural state.
Synthesis route :
The synthesis of Methyl Benzoate can be made by esterification between benzoic acid and methanol, by acid catalysis.
Regulations & IFRA
This ingredient is not restricted
