Verdox® (CAS N° 88-41-5)​

Photo credits: ScenTree SAS

Fruity > Green Fruits > Dry Woods > Green > Camphoric

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

Verdox® (CAS N° 88-41-5)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications Purity Latin name Treated part Geographical origin MOQ
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Verdox® - 30gr - Visit website Je me procure cet ingrédient - - - - - -

Verdox® - 30gr

Certifications :

Information Générales

General Presentation

  • CAS N° : 88-41-5

  • EINECS number : 201-828-7

  • FEMA number : Donnée indisponible.

  • FLAVIS number : Donnée indisponible.

  • JECFA number : Donnée indisponible.

  • Appearance : Colorless liquid

  • Density : 0,942

  • Volatility : Heart

  • Price Range :

Physico-chemical properties

  • Molecular formula : C12H22O2

  • Molecular Weight : 198,31 g/mol

  • Log P : 4,23

  • Fusion Point : 27°C

  • Boiling Point : 232°C

  • Detection Threshold : Donnée indisponible.

  • Optical rotation : Donnée indisponible

  • Vapor pressure : Donnée indisponible

  • Refractive Index @20°C : Donnée indisponible

  • Acid Value : Donnée indisponible.

  • Flash Point : 91°C

Utilisation

Uses

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

Natural availability :

Verdox® is not available in its natural state.

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.

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.

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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