4082-55-7

Basic information

• Product Name: METHYL NONACOSANOATE
• Synonyms: METHYL NONACOSANOATE;nonacosanoic acid methyl ester;methyl nonacosan-1-oate;METHYL NONACOSANOATE, STANDARD FOR GC
• CAS NO: 4082-55-7
• Molecular Formula: C₃₀H₆₀O₂
• Molecular Weight: 452.8
• EINECS: 223-808-7
• Product Categories: Fatty AcidsAlphabetic;Lipid Analytical Standards;M;META - METHFA/FAME/Lipids/Steroids;Neats&Single Component Solutions;Other Lipid Related Products;FAMEs
• Mol File: 4082-55-7.mol

Chemical Properties

• Melting Point: 69-72 °C
• Boiling Point: 467.1°Cat760mmHg
• Flash Point: 235.6°C
• Appearance: /
• Density: 0.858g/cm³
• Vapor Pressure: 6.67E-09mmHg at 25°C
• Refractive Index: 1.454
• Storage Temp.: 2-8°C
• CAS DataBase Reference: METHYL NONACOSANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL NONACOSANOATE(4082-55-7)
• EPA Substance Registry System: METHYL NONACOSANOATE(4082-55-7)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 4082-55-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C30H60O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30(31)32-2/h3-29H2,1-2H3

Upstream product

• 111514-97-7 8-[2-(5-Hexadecyl-thiophen-2-yl)-[1,3]dithiolan-2-yl]-octanoic acid methyl ester 
• 1057386-68-1 C₃₀H₅₈O₂ 
• 67-56-1 methanol 
• 111514-86-4 9-(5-Hexadecyl-thiophen-2-yl)-9-oxo-nonanoic acid methyl ester 
• 56555-02-3 methyl 9-chloro-9-oxononanoate 
• 83027-72-9 2-hexadecylthiophene 
• 63632-65-5 11-iodo-undecanoic acid 
• 2834-05-1 11-bromoundecanoic acid 
• 112-38-9 10-undecenoic acid 
• 929-33-9 methyl 11-iodoundecanoate 
• 112-89-0 1-Bromooctadecane 
• 4886-53-7 12.15.18-Trioxo-nonacosansaeure-tris-ethylenthio-ketal 

Downstream Products

• 6624-76-6 1-nonacosanol 
• 4250-38-8 n-nonacosanoic acid 

Relevant articles and documents

Two triterpenyl fatty acid esters from fagonia cretica as lipoxygenase inhibitors

Two triterpenyl fatty acid esters were isolated from the chloroform soluble fraction of Fagonia cretica and their structures elucidated as 3β-12-ursen-3yl-docosanoate (1) and 3β-12-ursen-3yl-nonacosanoate (2) by 1D-NMR, 2D-NMR, mass spectrometric and chemical analyses. Both new compounds were also evaluated for their lipoxygenase inhibitory potential using Baicalein as a standard.

C-GLYCOLIPIDS WITH ENHANCED TH-1 PROFILE

The invention is directed to novel synthetic C-glycolipids that selectively induce a ThI -type immune response characterized by enhanced IL- 12 secretion and increased activation of dendritic cells. The compounds of the invention are thereby useful in treating infections, cancers, cell proliferative disorders, and autoimmune diseases, both directly and as adjuvants.

Synthesis of Very Long Fatty Acid Methyl Esters

Phosphoranes, produced by treating alkyltriphenylphosphonium bromides with lithium hexamethyldisilazide, reacted with ω-oxo esters to give modest yields of the corresponding methyl cis-alkenoates.By an alternative method, treatment of ω-iodo esters with the complexes formed from reactions of alkylcopper(I) and Grignard reagents gave methyl alkanoates, cis-alkenoates, and methylene-interrupted cis,cis-alka-dienoates and cis,cis,cis-trienoates.The stereochemical integrity of the esters was determined by 13C NMR spectroscopy.

A New Synthesis of Long Chain Acid Esters and Carbinols

A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.