10030-74-7

Basic information

• Product Name: PALMITELAIDIC ACID METHYL ESTER
• Synonyms: METHYL TRANS-9-HEXADECENOATE;METHYL PALMITELAIDATE;C16:1 (TRANS-9) METHYL ESTER;DELTA 9 TRANS HEXADECENOIC ACID METHYL ESTER;PALMITELAIDIC ACID METHYL ESTER;TRANS-9-HEXADECENOIC ACID-METHYL ESTER;METHYL PALMITELAIDATE, STANDARD FOR GC;PALMITELAIDIC ACID METHYL ESTER 99%
• CAS NO: 10030-74-7
• Molecular Formula: C₁₇H₃₂O₂
• Molecular Weight: 268.43
• Mol File: 10030-74-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 394.2°Cat760mmHg
• Flash Point: 92.5°C
• Appearance: /liquid
• Density: 0.876g/cm³
• Vapor Pressure: 2.01E-06mmHg at 25°C
• Refractive Index: 1.452
• Storage Temp.: −20°C
• CAS DataBase Reference: PALMITELAIDIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: PALMITELAIDIC ACID METHYL ESTER(10030-74-7)
• EPA Substance Registry System: PALMITELAIDIC ACID METHYL ESTER(10030-74-7)

Safety Data

• WGK Germany: 3
• F: 8-10-23
• Hazardous Substances Data: 10030-74-7(Hazardous Substances Data)

Usage

Uses

Palmitelaidic Acid Methyl Ester is a derivative of Palmitoleic Acid (P144900), common constituent of triglycerides of human adipose tissue.

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+

Upstream product

• 67-56-1 methanol 
• 1120-25-8 (Z)-9-hexadecenoic acid methyl ester 
• 8001-22-7 soybean oil 

Downstream Products

• 1120-25-8 (Z)-9-hexadecenoic acid methyl ester 
• 123-99-9 azelaic acid 
• 111-14-8 oenanthic acid 

Relevant articles and documents

Potent Anti-HIV Ingenane Diterpenoids from Euphorbia ebracteolata

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

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.