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DOCOSYL FERULATE (50 MG)F0E1430.99MG/MG(AI) is a compound derived from Ferulic Acid (F308900), which is widely distributed in small amounts in plants. It is known for its antioxidant properties and is commonly used as a food preservative.

101927-24-6

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101927-24-6 Usage

Uses

Used in Food Industry:
DOCOSYL FERULATE (50 MG)F0E1430.99MG/MG(AI) is used as an antioxidant and food preservative for its ability to extend the shelf life of various food products and maintain their quality and freshness.
Used in Pharmaceutical Industry:
DOCOSYL FERULATE (50 MG)F0E1430.99MG/MG(AI) is used as a pharmaceutical ingredient for its potential health benefits, such as its antioxidant properties that may help protect cells from damage and support overall health.
Used in Cosmetic Industry:
DOCOSYL FERULATE (50 MG)F0E1430.99MG/MG(AI) is used as a cosmetic ingredient for its antioxidant properties, which may help protect the skin from environmental damage and support skin health.

Check Digit Verification of cas no

The CAS Registry Mumber 101927-24-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,2 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 101927-24:
(8*1)+(7*0)+(6*1)+(5*9)+(4*2)+(3*7)+(2*2)+(1*4)=96
96 % 10 = 6
So 101927-24-6 is a valid CAS Registry Number.

101927-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name docosyl (E)-ferulate

1.2 Other means of identification

Product number -
Other names Docosyl Ferulate

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:101927-24-6 SDS

101927-24-6Downstream Products

101927-24-6Relevant articles and documents

Ferulic Acid Esters and Withanolides: In Search of Withania somnifera GABAA Receptor Modulators

Sonar, Vijay P.,Fois, Benedetta,Distinto, Simona,Maccioni, Elias,Meleddu, Rita,Cottiglia, Filippo,Acquas, Elio,Kasture, Sanjay,Floris, Costantino,Colombo, Daniele,Sissi, Claudia,Sanna, Enrico,Talani, Giuseppe

, p. 1250 - 1257 (2019)

Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three known withanolides (3-5), a ferulic acid dimeric ester (6), and an inseparable mixture of three long alkyl chain ferulic acid esters (7-9), were isolated from a GABAA receptor positive activator methanol extract of the roots of Withania somnifera. The structures of the isolated compounds were elucidated based on NMR, MS, and ECD data analysis. In order to bioassay the single ferulic acid derivatives, compounds 6-9 were also synthesized. The most active compound, docosanyl ferulate (9), was able to enhance the GABAA receptor inhibitory postsynaptic currents with an IC50 value of 7.9 μM. These results, by showing an ability to modulate the GABAA receptor function, cast fresh light on the biological activities of the secondary metabolites of W. somnifera roots.

Impact of alkyl esters of caffeic and ferulic acids on tumor cell proliferation, cyclooxygenase enzyme, and lipid peroxidation

Jayaprakasam, Bolleddula,Vanisree, Mulabagal,Zhang, Yanjun,Dewitt, David L.,Nair, Muraleedharan G.

, p. 5375 - 5381 (2008/04/03)

The antioxidant ferulic and caffeic acid phenolics are ubiquitous in plants and abundant in fruits and vegetables. We have synthesized a series of ferulic and caffeic acid esters and tested for tumor cell proliferation, cyclooxygenase enzymes (COX-1 and -2) and lipid peroxidation inhibitory activities in vitro. In the tumor cell proliferation assay, some of these esters showed excellent growth inhibition of colon cancer cells. Among the phenolics esters assayed, compounds 10 (C12-caffeate), 11 (C16-caffeate), 21 (C 8-ferulate), and 23 (C12-ferulate) showed strong growth inhibition with IC50 values of 16.55, 13.46, 18.67, and 7.57 μg/mL in a breast cancer cell line; 9.65, 7.45, 17.05, and 4.35 μg/ mL in a lung cancer cell line; 5.78, 3.5, 4.29, and 2.46 μg/mL in a colon cancer cell line; 12.04, 12.21, 14.63, and 8.09 μg/ mL in a central nervous system cancer cell line; and 8.62, 7.76, 11.0, and 5.37 in a gastric cancer cell line. In COX enzyme inhibitory assays, ferulic and caffeic acid esters significantly inhibited both COX-1 and COX-2 enzymes. Caffeates 5-10 (C4-C 12), inhibited COX-1 enzyme between 50% and 90% and COX-2 enzyme by about 70%, whereas ferulates 15-21 (C3-C8) inhibited COX-1 and COX-2 enzymes by 85-95% 25 μg/mL. Long-chain caffeates 11-14 (C 16-C22) and short-chain ferulates 15-20 (C 3-C5) were the most active in lipid peroxidation inhibition and showed 60-70% activity at 5 μg/mL concentration.

Alkyl ferulates in wound healing potato tubers.

Bernards,Lewis

, p. 3409 - 3412 (2007/10/02)

Seven ferulic acid esters of 1-alkanols ranging in carbon length from C16 to C28 were synthesized and an HPLC protocol for their separation developed. Extracts prepared from wound healing potato (Solanum tuberosum) tubers and analysed by HPLC indicated th

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