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10030-74-7

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10030-74-7 Usage

Description

Palmitelaidic Acid Methyl Ester (PAME) is a derivative of Palmitoleic Acid, which is a common constituent of triglycerides found in human adipose tissue. It is a fatty acid ester with potential applications in various industries due to its unique properties.

Uses

Used in Pharmaceutical Industry:
PALMITELAIDIC ACID METHYL ESTER is used as a pharmaceutical compound for its potential therapeutic effects. The ester form of Palmitoleic Acid may offer enhanced bioavailability and targeted delivery, making it a promising candidate for drug development.
Used in Cosmetics Industry:
PALMITELAIDIC ACID METHYL ESTER is used as an ingredient in the cosmetics industry for its moisturizing and skin-conditioning properties. Its ability to penetrate the skin and improve its barrier function may contribute to the development of skincare products.
Used in Food Industry:
PALMITELAIDIC ACID METHYL ESTER is used as an additive in the food industry for its emulsifying and stabilizing properties. It may be utilized in the production of processed foods, where it can help improve texture and extend shelf life.
Used in Research:
PALMITELAIDIC ACID METHYL ESTER is used as a research tool for studying the biological effects of Palmitoleic Acid and its derivatives. It can be employed in laboratory experiments to better understand the role of fatty acids in various physiological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 10030-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10030-74:
(7*1)+(6*0)+(5*0)+(4*3)+(3*0)+(2*7)+(1*4)=37
37 % 10 = 7
So 10030-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19-2/h8-9H,3-7,10-16H2,1-2H3/b9-8+

10030-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl trans-9-hexadecenoate C16:1

1.2 Other means of identification

Product number -
Other names Palmitelaidic 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:10030-74-7 SDS

10030-74-7Relevant articles and documents

Potent Anti-HIV Ingenane Diterpenoids from Euphorbia ebracteolata

Huang, Ya-Si,Lu, Yan,Chen, Chin-Ho,Lee, Kuo-Hsiung,Chen, Dao-Feng

, p. 1587 - 1592 (2019/07/03)

Two new (1 and 2) and 14 known (3-16) ingenane diterpenoids were isolated from the roots of Euphorbia ebracteolata by bioassay-guided fractionation together with UPLC-MSn analysis. The absolute configurations of the new diterpenoids were established from electronic circular dichroism (ECD) data and ECD calculations. Except for ingenol (16), the ingenane diterpenoids with long aliphatic chain substituents (1-15) exhibited potent activities against HIV-1, with IC50 values of 0.7 to 9.7 nM and selectivity index values of 96.2 to 20 263. From the results, it was concluded that long aliphatic chain substituents are required for the enhanced anti-HIV activity of ingenane diterpenoids.

SINGLE-STAGE ESTERIFICATION OF OILS AND FATS

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Page/Page column 10-12, (2008/06/13)

A process for producing alkyl esters useful as biofuels and/or lubricants. An alkyl ester product produced by the process. The process comprises a single- stage reaction for esterifying a de-watered glyceride-containing feedstock with an anhydrous short chain alcohol in the presence of a basic esterification catalyst to produce a reaction product comprising alkyl esters and a reaction by-product comprising glycerol-containing substances and the catalyst-containing alcohol. The single-stage esterification reaction is conducted within a temperature and negative-pressure controllable vessel. The alkyl ester product is separated from the reaction by-product and may be further de-watered and/or purified. The catalyst-containing alcohol may be separated from the reaction by-product, de- watered and reused. The glycerol-containing substances may be separated from the reaction by-product and further purified. Useful glyceride-containing feedstocks include those prepared from plant or animal or fish materials, particularly those produced from seeds of mustard, canola, soybean, corn, cotton, flax and palm.

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