(3beta,24xi)-stigmast-5-en-3-ol

  • Name:(3beta,24xi)-stigmast-5-en-3-ol
  • CAS:19044-06-5
  • Purity:99%
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Details

Chinese Manufacturer Supply (3beta,24xi)-stigmast-5-en-3-ol 19044-06-5 On Stock with Competitive Price

  • Molecular Formula:C29H50O
  • Molecular Weight:414.715
  • Boiling Point:501.9°Cat760mmHg 
  • Flash Point:220.4°C 
  • PSA：20.23000 
  • Density:0.97g/cm3 
  • LogP:8.02480 

19044-06-5 Relevant articles

Process for recovery of plant sterols from by-product of vegetable oil refining

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Page/Page column 5-6, (2008/06/13)

The process for recovery of plant sterol...

Stereochemistry in the Hydrogenation of Steroidal (22R)- and (22S)-Δ24-26,22-Lactones

Iwadate, Hiroshi,Gamoh, Keiji,Fujimoto, Yoshinori,Ikekawa, Nobuo

, p. 2061 - 2065 (2007/10/02)

Catalytic hydrogenation of the (22R)-uns...

Side Chain Structural Requirement for Utilization of Sterols by the Silkworm for Growth and Development. Non-stereoselective Utilization of the 24-Stereoisomeric Pairs of 24-Alkylsterols

Fujimoto, Yoshinori,Kimura, Miki,Khalifa, Fathy A. M.,Ikekawa, Nobuo

, p. 4372 - 4381 (2007/10/02)

Four C-24 epimeric pairs of 24-alkylster...

Chemical constituents of Echites hirsuta (Apocynaceae)

Chien,Svoboda,Schiff Jr.,Slatkin,Knapp

, p. 247 - 249 (2007/10/05)

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19044-06-5 Process route

sterols; esterified

sterols; esterified

(3S,10R,13R,17R)-10,13-Dimethyl-17-(1,4,5-trimethyl-hexyl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
474-62-4,4651-51-8,23929-42-2,130061-65-3,139403-47-7

(3S,10R,13R,17R)-10,13-Dimethyl-17-(1,4,5-trimethyl-hexyl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

stigmasterol
83-48-7,481-16-3,14375-01-0,32345-19-0,72903-53-8,76250-40-3,80735-61-1,125636-86-4,130061-66-4,139685-48-6

stigmasterol

Sitosterol
83-46-5,83-47-6,5779-62-4,19044-06-5,31793-83-6,125636-84-2,130062-49-6

Sitosterol

brassicasterol
474-67-9,1105-10-8,2638-57-5,17472-78-5,51744-68-4,57637-04-4,130061-63-1,138752-55-3

brassicasterol

sterols; mixture of

sterols; mixture of

Conditions
Conditions Yield
With methanol; sodium methylate; at 60 ℃; for 2h; Heating / reflux;
Sitosterol
83-46-5,83-47-6,5779-62-4,19044-06-5,31793-83-6,125636-84-2,130062-49-6

Sitosterol

Conditions
Conditions Yield
3R-<2-14C(5R)-5-3H>MVA, Larix decidna;
β-Sitosterol-β-D-glucosid, HCl;
Glycosid von Sitosterol, Acid-Hydrolyse;
entspr. reines Acetat, methanol. KOH, A., 20grad, Verseifung;
O-Acetyl-22,23-dihydro-stigmasterin IX, 5percentig. methanol. KOH;
Verb. C, HCl, Hydrolyse;
3-Acetoxy-sitostadien-(3,5), 1.) NaBH4, sd. A., Red., 2.) wss. NaOH, Verseifung, 3.) Digitonin, Trennung v. α-Verb.;
(yield);
β-Sitosterin-D-glucosid, HCl;
Acetat 3, NaOH;
Phytosterin;
aus Rhizomen von Cimicifuga simplex;
entspr. β-D-Glucosid, saure Hydrolyse;
aus Samen von Derris robusta;

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