Verdox®
OTBCH acetate (OrthoTertButylCycloHexanol) ; (2-tert-butylcyclohexyl) acetate ; 1-acetoxy-2-tert-butylcyclohexane ; Agrumex HC ; 2-tert-butyl cyclohexanol acetate ; Ortho-tert-butyl cyclohexyl acetate ; 2-(1,1- dimethylethyl)cyclohexyl acetate ; Green acetate ; Grumex ; Menthonate ; Ommelione supra ; Ortholate ; Polarvert ; Pommelione supra ; Ylanat ortho
Photo credits: ScenTree SAS
| Company | Ingredient Name | ID | Naturality | Purity | Latin name | Treated part | Geographical origin | Certifications | Comments | MOQ |
|---|---|---|---|---|---|---|---|---|---|---|
|
Verdox® - 30gr | - | - | - | - | - | - | more | - |
General Presentation
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CAS N° : : 88-41-5
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EINECS number : 201-828-7
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FEMA number : Donnée indisponible.
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Density : 0,942
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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
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 232°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H22O2
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Log P : 4,23
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Molecular Weight : 198,31 g/mol
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Fusion Point : 27°C
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Flash Point : 91°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
In comparision to Vertenex®, Verdox® has a more fruity note, reminiscent of apple, before also being woody.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Verdox® is used in woody, coniferous, apple and fruity tea notes. Sometimes used as a Beta-Damascenone® replacer. Used for its stability in shampoos and shower gels.
Year of discovery :
1956
Isomerism :
Verdox® is a mixture of isomers, of which the cis isomer is present in majority, representing 60 to 95% of the mixture. One of the positional isomers of Verdox® is Vertenex®, with a woodier smell. Citronellyl acetate and Menthanyl acetate are constitutional isomers of Verdox®. Their smell is distinctly different, and although they also are fruity, they do not have a woody note.
Synthesis precursor :
Verdox® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Verdox® is not available in its natural state.
Synthesis route :
Verdox® is synthesized from 2-tert-butylcyclohexanol (obtained from 2-tert-butylphenol by a catalytic hydrogenation) by an esterification reaction with acetic anhydride, catalysed by a strong concentrated acid such as sulfuric acid.
Regulations & IFRA
This ingredient is not restricted
