19044-06-5 Usage
Description
(3beta,24xi)-stigmast-5-en-3-ol, a phytosterol belonging to the group of naturally occurring compounds found in plants, is a type of sterol that is structurally similar to cholesterol. It is found in various plant-based foods such as nuts, seeds, and vegetable oils and is known for its potential health benefits, including lowering cholesterol levels, reducing the risk of heart disease, and exhibiting anti-inflammatory and antioxidant properties. Furthermore, it has been studied for its potential use in skincare and cosmetic products due to its moisturizing and soothing effects on the skin.
Uses
Used in Health and Nutrition Industry:
(3beta,24xi)-stigmast-5-en-3-ol is used as a dietary supplement for its potential role in lowering cholesterol levels and reducing the risk of heart disease. Its presence in plant-based foods contributes to a healthy diet and supports cardiovascular health.
Used in Pharmaceutical Industry:
(3beta,24xi)-stigmast-5-en-3-ol is used as a pharmaceutical ingredient for its anti-inflammatory and antioxidant properties, which can be beneficial in the development of treatments for various inflammatory and oxidative stress-related conditions.
Used in Skincare and Cosmetic Industry:
(3beta,24xi)-stigmast-5-en-3-ol is used as an active ingredient in skincare and cosmetic products for its moisturizing and soothing effects on the skin, making it a valuable component in formulations aimed at improving skin health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 19044-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19044-06:
(7*1)+(6*9)+(5*0)+(4*4)+(3*4)+(2*0)+(1*6)=95
95 % 10 = 5
So 19044-06-5 is a valid CAS Registry Number.
19044-06-5Relevant articles and documents
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 sterols and tocopherols from deodorization distillates formed during chemical or physical refining of vegetable oils consists of the following steps: free fatty acids are removed from the deodorization distillate by vacuum distillation or by continuation solvent saponification, after the removal of free fatty acids, the received material is reacted with an aromatic carboxylic acid anhydride at a temperature of 50-150° C., under reduced pressure, after the treatment with anhydride, tocopherols are removed from the mixture, and crystalline free sterols are recovered from the distillation residue containing sterol esters, di- and triglycerides by transesterification.
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-alkylsterols 1-8 were stereoselectively synthesized via orthoester Claisen rearrangement of the (22)R or (22S)-Δ23Z steroid derivatives (11 and 12).These compounds were tested on the silkworm larvae, Bombyx mori, in order to examine the relationship of the C-24 stereochemical arrangement and utilizability as a nutrient sterol.All of the tested sterols effectively supported the growth and development of the insect and were converted into cholesterol regardless of the C-24 configuration.Keywords - 24-alkylcholesterol; 24-alkyl-22-dehydrocholesterol; orthoester Claisen rearrangement; stereoselective synthesis; insect sterol; silkworm
Steroids from sponges
Sheikh,Djerassi
, p. 4095 - 4103 (2007/10/10)
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