82654-98-6

  • Product Name:Vanillyl Butyl Ether
  • Molecular Formula:C12H18O3
  • Purity:99%
  • Molecular Weight:210.273
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Product Details;

CasNo: 82654-98-6

Molecular Formula: C12H18O3

Appearance: Colorless transparent liquid

Quality Factory Supply Vanillyl Butyl Ether, Buy 82654-98-6 Fast Shipping

  • Molecular Formula:C12H18O3
  • Molecular Weight:210.273
  • Appearance/Colour:Colorless transparent liquid 
  • Vapor Pressure:0.000388mmHg at 25°C 
  • Refractive Index:n20/D 1.516(lit.)  
  • Boiling Point:307.9 ºC at 760 mmHg 
  • Flash Point:140 ºC 
  • PSA:38.69000 
  • Density:1.048 g/cm3 
  • LogP:2.71750 
  • IDLH:888 
  • IDLH:3796 

Vanillyl butyl ether(Cas 82654-98-6) Usage

Description

Vanillyl butyl ether is an ether of monohydroxybenzoic acid. It is added to food products as a flavoring agent. It is also present in cosmetics and personal care products. It has a characteristic trigeminal, burning, hot pepper nature and can be used in spice flavors like pepper, cinnamon and ginger, as well as blends for some baked applications, including cookies. It has some other applications include flavoring for alcoholic and non-alcoholic beverages with herbal, berry, vanilla, cola, ginger ale, root beer, hot chocolate, chai, ice tea and mints. It can also be used as a warming agent.

Chemical Properties

Vanillyl butyl ether has a weak, vanillic, acidic odor.

Uses

Vanillyl butyl ether is a compound hypothesized to have warming and vasodilation mechanisms when applied on the skin as a cream.

General Description

Vanillyl butyl ether is an alkoxy-substituted benzyl derivative mainly used as a flavoring agent.

Biochem/physiol Actions

Taste at 10-15%

Who Evaluation

Evaluation year: 2001

InChI:InChI=1/C12H18O3/c1-3-4-7-15-9-10-5-6-11(13)12(8-10)14-2/h5-6,8,13H,3-4,7,9H2,1-2H3

82654-98-6 Relevant articles

Synthetic method of vanillyl alcohol ether

-

Paragraph 0044-0046, (2019/07/08)

The invention discloses a synthetic meth...

Technology for preparing vanillyl alcohol ether by using one step method

-

Paragraph 0025; 0026, (2017/03/18)

The invention relates to a technology fo...

Sulfated tungstate as hydroxyl group activator for preparation of benzyl, including p-methoxybenzyl ethers of alcohols and phenols

Katkar, Kamlesh V.,Veer, Sachin D.,Akamanchi, Krishnacharya G.

supporting information, p. 1893 - 1901 (2016/11/25)

Sulfated tungstate was found to be an ef...

Direct synthesis of unsymmetrical ethers from alcohols catalyzed by titanium cation-exchanged montmorillonite

Mitsudome, Takato,Matsuno, Tsuyoshi,Sueoka, Shoichiro,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

supporting information; experimental part, p. 610 - 613 (2012/04/23)

Titanium-exchanged montmorillonite (Ti4+...

82654-98-6 Process route

vanillin
121-33-5,8014-42-4

vanillin

butan-1-ol
71-36-3

butan-1-ol

4-(butoxymethyl)-2-methoxyphenol
82654-98-6

4-(butoxymethyl)-2-methoxyphenol

Conditions
Conditions Yield
With hydrogen; at 20 ℃; for 18h; under 7500.75 Torr; Industrial scale;
96%
vanillin; butan-1-ol; With Pb/C; hydrogen; at 60 - 70 ℃; for 8h; under 13501.4 Torr;
With aluminum (III) chloride; at 60 - 70 ℃; for 12h;
68.55%
n-Butyl chloride
109-69-3

n-Butyl chloride

vanillin
121-33-5,8014-42-4

vanillin

4-(butoxymethyl)-2-methoxyphenol
82654-98-6

4-(butoxymethyl)-2-methoxyphenol

Conditions
Conditions Yield
With potassium borohydride; In ethyl acetate; at 30 - 40 ℃; for 3h;
90.51%

82654-98-6 Upstream products

  • 498-00-0
    498-00-0

    4-hydroxymethyl-2-methoxyphenol

  • 71-36-3
    71-36-3

    butan-1-ol

  • 121-33-5
    121-33-5

    vanillin

  • 109-69-3
    109-69-3

    n-Butyl chloride

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