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75190-82-8

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75190-82-8 Usage

Description

CIS-10-HEPTADECENOIC ACID METHYL ESTER, also known as (10Z)-10-Heptadecenoic Acid Methyl Ester, is a naturally occurring compound found in blackberry seed oil. It is characterized by its antioxidant properties and its ability to suppress allergic inflammation in human basophilic KU812F cells. This versatile compound has potential applications in various industries due to its unique characteristics.

Uses

Used in Pharmaceutical Industry:
CIS-10-HEPTADECENOIC ACID METHYL ESTER is used as an anti-inflammatory agent for its ability to suppress allergic inflammation in human basophilic KU812F cells. This property makes it a promising candidate for the development of treatments for various allergic conditions and inflammatory diseases.
Used in Nutraceutical Industry:
CIS-10-HEPTADECENOIC ACID METHYL ESTER is used as a natural antioxidant for its antioxidant activity. It can be incorporated into various health supplements and functional foods to provide consumers with the benefits of its antioxidant properties, which may help protect cells from damage caused by free radicals and support overall health.
Used in Cosmetic Industry:
CIS-10-HEPTADECENOIC ACID METHYL ESTER is used as an ingredient in cosmetic products for its anti-inflammatory and antioxidant properties. It can be utilized in the development of skincare products aimed at reducing inflammation and promoting skin health, as well as in products designed to protect the skin from oxidative stress caused by environmental factors.
Used in Food Industry:
CIS-10-HEPTADECENOIC ACID METHYL ESTER is used as a natural antioxidant in the food industry to extend the shelf life of various products by protecting them from oxidative degradation. Its addition to the food supply can help maintain the quality, taste, and nutritional value of the products while also providing health benefits due to its antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 75190-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75190-82:
(7*7)+(6*5)+(5*1)+(4*9)+(3*0)+(2*8)+(1*2)=138
138 % 10 = 8
So 75190-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20-2/h8-9H,3-7,10-17H2,1-2H3/b9-8-

75190-82-8SDS

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 methyl heptadec-10-enoate

1.2 Other means of identification

Product number -
Other names METHYL 10C-HEPTADECENOATE

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:75190-82-8 SDS

75190-82-8Downstream Products

75190-82-8Relevant articles and documents

Quantification of Nonanal and Oleic Acid Formed during the Ozonolysis of Vegetable Oil Free Fatty Acids or Fatty Acid Methyl Esters

Tavassoli-Kafrani,Foley,Kharraz,Curtis

, p. 303 - 310 (2016/03/08)

The ozonolysis of unsaturated lipids is a process that has been used to generate aldehydes, acids, alcohols, and other biobased chemical intermediates. Reported here is a method that can be used to measure the formation of nonanal and oleic acid during the ozonolysis of unsaturated vegetable oil fatty acids or their methyl esters to indicate the extent of the ozonolysis reaction. Derivatization was performed using boron trifluoride in methanol solution to transform nonanal and oleic acid into nonanal dimethyl acetal and oleic acid methyl ester, respectively. Undecanal and 10-heptadecenoic acid were used as internal standards and separation was performed using gas chromatography coupled with a flame ionization detector. The method was validated by performing a standard addition procedure in which nonanal or oleic acid standards were spiked into samples collected during the ozonolysis of oleic acid or canola oil fatty acid methyl ester (FAME). Linear regression results indicated that the measured nonanal and oleic acid are in good agreement with the actual amounts of nonanal and oleic acid added to the sample with at least 98 % recovery. The application of the method was demonstrated by the successful measurement of nonanal and oleic acid formed throughout the ozonolysis process for high oleic canola oil FAME.

DIRECT METHOD AND REAGENT KITS FOR FATTY ACID ESTER SYNTHESIS

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Page/Page column 18; 20-21; 27, (2008/12/07)

Provided are efficient, cost-effective and water tolerant methods (e.g., single-vial methods) for preparing fatty acid esters from organic matter, comprising: obtaining organic matter comprising at least one fat substituent, contacting the organic matter in a reaction mixture with a basic solution under conditions suitable to provide for hydrolytic release of monomeric fatty acids from the at least one fat substituent to provide a base-treated reaction mixture, and esterifying the monomeric fatty acids of the base-treated reaction mixture by acidification of the reaction mixture and treating in the presence of an organic alcohol to provide fatty acid esters. The methods optionally further comprise, prior to esterifying, neutralizing the base-treated reaction mixture to provide for neutralized fatty acids, separating the neutralized fatty acids from the neutralized reaction mixture, and dissolving the separated fatty acids in the esterification reaction mixture. Also provided are related methods and kits for fat analysis.

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