23696-85-7

  • Product NameDamascenone
  • Molecular FormulaC13H18O
  • Molecular Weight190.285
  • Purity99%
  • AppearanceCOLORLESS LIQUID
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Product Details

Quick Details

  • CasNo: 23696-85-7
  • Molecular Formula: C13H18O
  • Appearance: COLORLESS LIQUID
  • Purity: 99%

Factory Supply Industrial Grade Damascenone 23696-85-7 with Best Price

  • Molecular Formula:C13H18O
  • Molecular Weight:190.285
  • Appearance/Colour:COLORLESS LIQUID 
  • Vapor Pressure:0.00503mmHg at 25°C 
  • Refractive Index:1.350-1.380 
  • Boiling Point:275.6 °C at 760 mmHg 
  • Flash Point:111 °C 
  • PSA:17.07000 
  • Density:0.926 g/cm3 
  • LogP:3.43420 

Damascenone(Cas 23696-85-7) Usage

Preparation

By treating the corresponding ethyl safranate with allyl lithium, followed by catalytic isomerization of the reaction product; also from the oxirane derivative of β-damascone by an acid-catalyzed reaction.

Biochem/physiol Actions

Taste at 1-5 ppm

Aroma threshold values

Detection: 0.0007 to 0.009 ppb. Aroma characteristics at 1.0%: sweet, brown woody, tobacco, davana-like fruity, with a spicy balsamic undernote.

Taste threshold values

Taste characteristics at 1 to 5 ppm: sweet brown, tea-like, davana dried fruity, with jamy berry, strawberry and raspberry nuances, woody, floral, herbal, green and fruity with spicy tobacco nuances.

General Description

Damascenone is a norisoprenoid ketone mainly found in red wines. It occurs naturally in tomato and grapes.

InChI:InChI=1/C13H18O/c1-5-7-11(14)12-10(2)8-6-9-13(12,3)4/h5-8H,9H2,1-4H3

23696-85-7 Relevant articles

Method for synthesizing beta-damascenone

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, (2019/01/14)

The invention discloses a method for syn...

A β- malaysian ketene method for the preparation of perfume

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Paragraph 0049-0050, (2017/03/14)

The invention discloses a preparation me...

Industrial manufacturing method of damascenone

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Paragraph 0047-0049, (2017/05/06)

The invention provides an industrial man...

23696-85-7 Process route

1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-buten-1-one
35044-68-9

1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-buten-1-one

1-(2,6,6-trimethyl-1,3-cyclohexadiene-1-yl)-2-butene-1-one
23696-85-7

1-(2,6,6-trimethyl-1,3-cyclohexadiene-1-yl)-2-butene-1-one

Conditions
Conditions Yield
With N-Bromosuccinimide; sodium sulfate; dibenzoyl peroxide; In benzene; at 50 ℃; for 3h; Inert atmosphere;
88.6%
(E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene
53941-13-2

(E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene

1-(2,6,6-trimethyl-1,3-cyclohexadiene-1-yl)-2-butene-1-one
23696-85-7

1-(2,6,6-trimethyl-1,3-cyclohexadiene-1-yl)-2-butene-1-one

Conditions
Conditions Yield
With pyridine; chromium(VI) oxide; In dichloromethane; at 20 - 30 ℃; for 1h; Reagent/catalyst; Temperature; Solvent;
161 g

23696-85-7 Upstream products

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    35044-68-9

    1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-buten-1-one

  • 79-77-6
    79-77-6

    4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one

  • 53941-13-2
    53941-13-2

    (E)-2-(2-butenyl)-1,3,3-trimethyl-1-cyclohexene

  • 61899-98-7
    61899-98-7

    2,6,6-trimethylcyclohex-2-en-1-ylidene ketene

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