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57818-40-3

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57818-40-3 Usage

Description

3,4-DiMethyl-5-pentyl-2-furannonanoic Acid, also known as F3 furan fatty acid, is a type of furan fatty acid that is predominantly found in algae and fish, although it is also produced by plants and microorganisms. 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid possesses unique chemical properties, including radical-scavenging ability and anti-inflammatory properties, which make it a valuable compound for various applications.

Uses

Used in Pharmaceutical Industry:
3,4-DiMethyl-5-pentyl-2-furannonanoic Acid is used as a therapeutic agent for its anti-inflammatory properties, which can help in the treatment of various inflammation-related conditions. Its radical-scavenging ability also contributes to its potential use in the development of drugs targeting oxidative stress-related diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid is used as a functional ingredient due to its health-promoting properties. Its presence in algae and fish makes it a natural and beneficial component that can be incorporated into dietary supplements and fortified foods.
Used in Cosmetic Industry:
3,4-DiMethyl-5-pentyl-2-furannonanoic Acid is used as an active ingredient in the cosmetic industry, where its anti-inflammatory and radical-scavenging properties can be harnessed for the development of skincare products aimed at reducing inflammation and promoting skin health.
Used in Food Industry:
In the food industry, 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid is used as a natural preservative and antioxidant, helping to extend the shelf life of products and maintain their quality by neutralizing harmful free radicals and reducing inflammation in the body.
Overall, 3,4-DiMethyl-5-pentyl-2-furannonanoic Acid is a versatile compound with a wide range of applications across different industries, primarily due to its unique properties and natural occurrence in various sources.

Check Digit Verification of cas no

The CAS Registry Mumber 57818-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,1 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57818-40:
(7*5)+(6*7)+(5*8)+(4*1)+(3*8)+(2*4)+(1*0)=153
153 % 10 = 3
So 57818-40-3 is a valid CAS Registry Number.

57818-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(3,4-dimethyl-5-pentylfuran-2-yl)nonanoic acid

1.2 Other means of identification

Product number -
Other names 2-Furannonanoic acid,3,4-dimethyl-5-pentyl

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:57818-40-3 SDS

57818-40-3Downstream Products

57818-40-3Relevant articles and documents

167. Ueber die Strukturaufklaerung von (Hydroxy-oxo-cyclopentenyl)alkansaeuren, den Aldolkondensationsprodukten von Dioxoencarbonsaeuren aus Rinderleber

Schoedel, Rolf,Spiteller, Gerhard

, p. 1624 - 1634 (2007/10/02)

During homogenization of cattle liver the highly instable dioxoene acids 13a, 13b, and 13c are formed.These acids cyclize in alkaline solution to yield pairs of stable (hydroxy-oxo-cyclopentenyl)alkanoic acids, which were isolated as methyl esters 4a/5a, 4b/5b, and 4c/5c.The structures of these compounds were deduced from an enriched 3-mg mixture sample by microchemical reactions combined with a GC/MS analysis of the reaction products.Compound 13a was obtained as methyl ester by oxidation of the methyl ester of the corresponding F-acid with NaOCl.It was not possible to isolate 13a in pure form due to its high sensitivity.Instead of the methyl ester of 13a, 4a and 5a were isolated, of which the structures were established.

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