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Faradiol, also known as 18a,19bH-Urs-20-ene-3b,16b-diol or 16b-Hydroxypseudotaraxasterol, is a triterpenoid diol found in plants such as *Calendula officinalis*. It exhibits notable anti-inflammatory and skin-protective properties, primarily attributed to its ability to modulate inflammatory mediators and promote tissue repair. Faradiol has been studied for its potential therapeutic applications in dermatology, particularly in wound healing and reducing skin irritation. Its mechanism of action may involve inhibition of pro-inflammatory cytokines and oxidative stress pathways, making it a promising candidate for topical formulations aimed at treating inflammatory skin conditions.

20554-95-4

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20554-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20554-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,5 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20554-95:
(7*2)+(6*0)+(5*5)+(4*5)+(3*4)+(2*9)+(1*5)=94
94 % 10 = 4
So 20554-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-18-11-14-28(6)24(32)17-30(8)20(25(28)19(18)2)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h11,19-25,31-32H,9-10,12-17H2,1-8H3/t19-,20-,21+,22?,23+,24+,25+,27+,28-,29-,30-/m1/s1

20554-95-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name faradiol

1.2 Other means of identification

Product number -
Other names Faradiol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20554-95-4 SDS

20554-95-4Upstream product

20554-95-4Relevant academic research and scientific papers

Terpenoids in four Inula species from Bulgaria

Aneva, Ina,Ivanova, Victoria,Staleva, Plamena,Todorova, Milka,Trendafilova, Antoaneta

, p. 1229 - 1240 (2022/02/16)

Phytochemical study of the chloroform extract of the aerial parts of Inula germanica L., I. ensifolia L., I. conyza (Griess.) DC. and I. salicina L. led to the identification of 33 terpenoids. β- and α-amyrin, lupeol, taraxasterol, ψ-taraxasterol and their 3-O-acetates and 3-O-palmitates were identified by GC/MS. In addition, the structures of 3-O-palmitates of mainaladiol, arnidiol, faradiol and 16-hydroxylupeol were confirmed by NMR. ent-Kaur-16-en-19- -oic acid and its 15α-(3-methylpentanoyloxy) and 15α-(3-methylbutanoyloxy) derivatives were isolated from I. conyza. Ten closely related sesquiterpene lactones (germacranolides and melampolides) were found in I. germanica and their structural identification was performed by spectral analyses. I. ensifolia and I. salicina were free of sesquiterpene lactones and diterpenoids. All triterpenoids and diterpenoids, grazielia acid, desacetylovatifolin and 8-(2-methylbutanoyloxy)- 1(10),4,11(13)-germacrutrien-6,12-olide-14-oic acid are described for the first time in the studied species. The principal component analysis was used to find a relationship between the investigated up to now Inula species, growing in Bulgaria.

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