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19788-74-0

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19788-74-0 Usage

Description

C19:1 (CIS-10) METHYL ESTER, also known as cis-10-Nonadecenoic acid methyl ester, is a fatty acid methyl ester that serves as a standard for the quantification of cis-nonadecenoic acid in various chromatography applications. It is a significant compound in the field of chemical analysis and research, particularly for the study and measurement of fatty acids.

Uses

Used in Chemical Analysis Industry:
C19:1 (CIS-10) METHYL ESTER is used as a reference standard for the accurate quantification of cis-nonadecenoic acid in chromatography applications. Its role is crucial in ensuring the precision and reliability of the results obtained from these analyses, which can be applied in various fields such as pharmaceuticals, food science, and environmental research.
Used in Research and Development:
In the research and development sector, C19:1 (CIS-10) METHYL ESTER is utilized as a benchmark for the study of fatty acid methyl esters and their potential applications. This includes the investigation of their properties, interactions, and potential uses in the development of new products and technologies.
Used in Quality Control:
C19:1 (CIS-10) METHYL ESTER is also employed in quality control processes to ensure the consistency and accuracy of chromatography methods and results. By using this compound as a reference, laboratories can validate their analytical techniques and maintain high standards in their research and testing procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 19788-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19788-74:
(7*1)+(6*9)+(5*7)+(4*8)+(3*8)+(2*7)+(1*4)=170
170 % 10 = 0
So 19788-74-0 is a valid CAS Registry Number.

19788-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl nonadec-2-enoate

1.2 Other means of identification

Product number -
Other names cis-10-nonadecenoic acid methyl ester

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:19788-74-0 SDS

19788-74-0Relevant articles and documents

Inhibition of oleamide hydrolase catalyzed hydrolysis of the endogenous sleep-inducing lipid cis-9-octadecenamide

Patterson, Jean E.,Ollmann, Ian R.,Cravatt, Benjamin F.,Boger, Dale L.,Wong, Chi-Huey,Lerner, Richard A.

, p. 5938 - 5945 (2007/10/03)

Oleamide (1, cis-9-octadecenamide) is a naturally occurring brain constituent that has been shown to accumulate and disappear under conditions of sleep deprivation and sleep recovery, respectively. Synthetic 1 has been found to induce sleep in a structurally specific manner at nanomolar quantities. Hydrolysis of 1 by an enzyme (oleamide hydrolase) present in the cell membrane rapidly degrades oleamide to oleic acid (cis-9-octadecenoic acid). Such observations suggest 1 may constitute a prototypical member of a class of fatty acid primary amide biological signaling molecules in which the diversity and selectivity of function are derived from the length of the alkane chain as well as the position, stereochemistry, and degree of unsaturation. A series of inhibitors of oleamide hydrolase were designed and prepared which were expected to derive their properties through interactions with the putative active site cysteine residue within oleamide hydrolase. This approach yielded a series of rapid, selective, and highly potent inhibitors (K(i) = 13 μM to 1 nM) which in addition to their potential therapeutic value may serve as useful tools to define the biological role of oleamide.

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