Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 821-55-6
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EINECS number : 212-480-0
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FEMA number : 2785
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Density : 0,82
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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 : Heart/Base
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Price Range : €€€
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Appearance : Colorless liquid
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FLAVIS number : 07.020
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JECFA number : 292
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 193°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C9H18O
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Log P : 2,71
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Molecular Weight : 142,24 g/mol
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Fusion Point : -21°C
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Flash Point : 79°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Stable in perfumes and in diverse bases.
Uses in perfumery :
Year of discovery :
Data not available.
Isomerism :
Methyl Heptyl Ketone is the constitutional isomer of Cinnamaldehyde, although these two molecules do not smell the same.
Synthesis precursor :
A condensation of this ketone with another ketone may form the desired alkene. Hydrogenation of Methyl Heptyl Ketone can form 2-nonanol, also relevant in perfumery.
Natural availability :
Methyl Heptyl Ketone is present in fruits and spice such as banana, ginger, clove, coconut, tomato, corn, cheese, wine.. Thus, natural qualities are available
Synthesis route :
Methyl Heptyl Ketone can be synthesized by dry distillation of Barium Caprylate and Barium acetate at very low pressure (0.5 to 2 mmHg). Another method for synthesizing this compound is to use chromic acid, reacting with methyl heptyl carbinol at room temperature, to oxidize the latter.
Regulations & IFRA
This ingredient is not restricted
