Allyl cyclohexyl propionate (CAS N° 2705-87-5)​

Photo credits: ScenTree SAS

Allyl cyclohexyl propionate

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Allyl 3-cyclohexyl propionate ; Allyl 3-cyclohexyl propanoate ; Allyl beta-cyclohexyl propionate ; Allyl beta-cyclohexyl propanoate ; Allyl cyclohexylpropanoate ; Allyl cyclohexylpropionate ; Allyl hexahydrophenylpropionate ; Allyl hexahydrophenylpropanoate ; Pineapple ester ; Prop-2-en-1-yl 3-cyclohexylpropionate ; Prop-2-en-1-yl 3-cyclohexylpropanoate ; 2-propenyl 3-cyclohexylpropanoate ; ACHP

Allyl cyclohexyl propionate (CAS N° 2705-87-5)​

Photo credits: ScenTree SAS



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PCW logo ALLYL CYCLOHEXYL PROPIONATE
ALCY-1
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Tilley Distribution logo Allyl Cyclohexyl Proprionate Discover Synthetic Aroma Chemicals - -
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ALLYL CYCLOHEXYL PROPIONATE

ALCY-1

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Allyl Cyclohexyl Proprionate
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General Presentation

General Presentation

  • CAS N° :

    2705-87-5
  • EINECS number :

    220-292-5
  • FEMA number :

    2026
  • FLAVIS number :

    9,498
  • JECFA number :

    13
  • Volatility :

    Head/Heart
  • Price Range :

    €€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,95
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    Donnée indisponible.
  • Flash Point :

    106°C (222,8°F)
  • Molecular formula :

    C12H20O2
  • Molecular Weight :

    196,29 g/mol
  • Log P :

    4,28
  • Fusion Point :

    < -20°C (< -4°F)
  • Boiling Point :

    266°C (510,8°F)
  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Allyl Cyclohexyl Propionate is used in fruity notes of pineapple to bring a tasty, sweet, natural note and acidity of the fruit. It is more commonly used in exotic fruits notes and in chamomille reconstitutions.

Year of discovery :

Data not available.

Natural availability :

Allyl Cyclohexyl Propionate is not reported as found in nature. It can't be extracted and used as natural.

Isomerism :

Allyl Cyclohexyl Propionate is a constitutional isomer of Isobornyl acetate and Terpenyl acetate among others, but they do not have the same smell as ACHP.

Synthesis precursor :

Allyl Cyclohexyl Propionate is not used for the synthesis of another compound of olfactive interest.

Synthesis route :

Allyl Cyclohexyl Propionate is synthesized on a synthetical way in two steps, from Cinnamic Acid. The first step is a catalytic hydrogenation of the acid, at very high temperature (over 200°C), using a catalyst as palladium. The second step is an esterification involving the intermediary product, cyclohexyl propionic acid, and allyl alcohol, i.e. 2-propenol. This reaction is heated and uses an acidic catalysor as concentrated sulfuric acid.

Stability :

Esters may form their corresponding acid in stability

Other comments :

In comparision to other notes of pineapple as Ethyl Butyrate, Allyl Caproate and Allyl Amyl Glycolate for example, CHPA brings a tasty and natural fruit note.

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