545-47-1

  • Product Name:Lupeol
  • Molecular Formula:C30H50O
  • Purity:99%
  • Molecular Weight:426.726
Inquiry

Product Details

pd_meltingpoint:215-216oC

Appearance:white powder

Purity 99% Min Lupeol 545-47-1 Spot Supply with Safe Transportation

  • Molecular Formula:C30H50O
  • Molecular Weight:426.726
  • Appearance/Colour:white powder 
  • Vapor Pressure:1.41E-11mmHg at 25°C 
  • Melting Point:215-216oC 
  • Refractive Index:1.515 
  • Boiling Point:488.1 °C at 760 mmHg 
  • PKA:15.19±0.70(Predicted) 
  • Flash Point:216.9 °C 
  • PSA:20.23000 
  • Density:0.978 g/cm3 
  • LogP:8.02480 

Lupeol(Cas 545-47-1) Usage

Definition

ChEBI: A pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in m ny edible fruits and vegetables.

General Description

Lupeol is a novel anti-cancer and anti-inflammatory dietary triterpene. They help in stabilizing phospholipid bilayers in plant cell membranes. In general, this group contains 28-29 carbons along with carbon-carbon double bonds, usually one in the sterol nucleus and at times a second in the alkyl side chain.

InChI:InChI=1/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21+,22-,23+,24-,25+,27+,28-,29+,30+/m0/s1

545-47-1 Relevant articles

Pentacyclic triterpenes and naphthoquinones from Euclea divinorum

Mebe, Paul P.,Cordell, Geoffrey A.,Pezzuto, John M.

, p. 311 - 313 (1998)

Phytochemical studies on Euclea divinoru...

TRITERPENOIDS OF AMSONIA GRANDIFLORA

Wahyuono, Subagus,Hoffmann, Joseph J.,Jolad, Shivanand D.,Dentali, Steven J.

, p. 1213 (1987)

Stems and leaves of Amsonia grandiflora ...

Antibacterial activity of naphthoquinones and triterpenoids from Euclea natalensis root bark

Weigenand, Oliver,Hussein, Ahmed A.,Lall, Namrita,Meyer, Jacobus J. M.

, p. 1936 - 1938 (2004)

Phytochemical studies of an ethanolic ex...

Synthesis of Lupeol from Betulin

Garifullina,Myasoedova, Yu. V.,Ishmuratova

, p. 765 - 767 (2019/08/07)

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Practical Synthesis of α-Amyrin, β-Amyrin, and Lupeol: The Potential Natural Inhibitors of Human Oxidosqualene Cyclase

Chen, Dongyin,Xu, Fengguo,Zhang, Pu,Deng, Jie,Sun, Hongbin,Wen, Xiaoan,Liu, Jun

, (2017/10/20)

A practical synthesis of α-amyrin (1), β...

And reclaims to clean rough synthesis method

-

Paragraph 0036-0041; 0053-0055, (2017/08/25)

The invention belongs to the research fi...

Lupeol-3-O-decanoate, a new triterpene ester from Cadaba farinosa Forssk. growing in Saudi Arabia

Al-Musayeib, Nawal M.,Mohamed, Gamal A.,Ibrahim, Sabrin R. M.,Ross, Samir A.

, p. 5297 - 5302 (2013/12/04)

A new triterpene ester (1) together with...

545-47-1 Process route

Pentadecanoic acid (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-yl ester

Pentadecanoic acid (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-1-isopropenyl-3a,5a,5b,8,8,11a-hexamethyl-icosahydro-cyclopenta[a]chrysen-9-yl ester

palmitic acid
1002-84-2

palmitic acid

lupenol
545-47-1

lupenol

Conditions
Conditions Yield
With sodium hydroxide; In chloroform; for 3h; Heating;
 
Glochidone
6610-55-5

Glochidone

lupenol
545-47-1

lupenol

lupenone
1617-70-5

lupenone

3-epilupeol
33869-84-0,55870-42-3,101627-40-1,107596-77-0,545-47-1,4439-99-0

3-epilupeol

Conditions
Conditions Yield
With potassium hydroxide; In diethylene glycol; for 2h; Heating;
40%
15%
8%

545-47-1 Upstream products

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    lupenone

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    aluminum isopropoxide

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    isopropyl alcohol

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    benzene

545-47-1 Downstream products

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    3β-Lupanol

  • 3186-86-5
    3186-86-5

    3β-Hydroxy-28-lupane

  • 1617-68-1
    1617-68-1

    lupeol acetate

  • 3186-72-9
    3186-72-9

    3-Oxolupane

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