5129-59-9

Basic information

• Product Name: METHYL 13-METHYLTETRADECANOATE
• Synonyms: 13-METHYLMYRISTIC ACID METHYL ESTER;ISO C15 METHYL ESTER;ISO-PENTADECANOIC METHYL ESTER;METHYL 13-METHYLTETRADECANOATE;13-methyldodecanoic acid methyl ester;methyl 13-methylmyristate;13-Methyltetradecanoic acid methyl ester
• CAS NO: 5129-59-9
• Molecular Formula: C₁₆H₃₂O₂
• Molecular Weight: 256.42
• Mol File: 5129-59-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 296.8°C at 760 mmHg
• Flash Point: 134.7°C
• Appearance: /
• Density: 0.864g/cm³
• Vapor Pressure: 0.0014mmHg at 25°C
• Refractive Index: 1.438
• Storage Temp.: 2-8°C
• CAS DataBase Reference: METHYL 13-METHYLTETRADECANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 13-METHYLTETRADECANOATE(5129-59-9)
• EPA Substance Registry System: METHYL 13-METHYLTETRADECANOATE(5129-59-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 5129-59-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H32O2/c1-15(2)13-11-9-7-5-4-6-8-10-12-14-16(17)18-3/h15H,4-14H2,1-3H3

Upstream product

• 67-56-1 methanol 
• 2485-71-4 13-methyltetradecanoic acid 
• 117582-43-1 Methyl 13-methyl-12-tetradecenoate 
• 170242-21-4 (2R,3R)-3-Hydroxy-2-(13'-methyltetradecanoylamino)-15-methylhexadecanesulfonic acid 
• 186581-53-3 diazomethane 
• 2009-59-8 methyl 11-formylundecanoate 
• 1501-82-2 cyclododecene 
• 14065-32-8 methyl 10-chloro-10-oxodecanoate 
• 818-88-2 sebacic acid mono methyl ester 
• 106-79-6 dimethyl sebacate 
• 95799-79-4 10-Keto-13-methyltetradecansaeuremethylester 
• 929-33-9 methyl 11-iodoundecanoate 
• 6287-90-7 11-bromo-undecanoic acid methyl ester 
• 2834-05-1 11-bromoundecanoic acid 

Downstream Products

• 66054-36-2 tunicamycin V 
• 2485-71-4 13-methyltetradecanoic acid 

Relevant articles and documents

Lutoside: An acyl-1-(Acyl-6'-mannobiosyl)-3-glycerol isolated from the Sponge-associated bacterium Micrococcus luteus

Lutoside, an unusual acyl-1-(acyl-6'-mannobiosyl)-3-glycerol 1 was isolated from the sponge-associated bacterial strain Microccocus luteus. Structure elucidation was performed by spectroscopic analysis and chemical transformations.

Structural identification of antibacterial lipids from Amazonian palm tree endophytes through the molecular network approach

A library of 197 endophytic fungi and bacteria isolated from the Amazonian palm tree Astrocaryum sciophilum was extracted and screened for antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). Four out of five antibacterial ethyl acetate extracts were also cytotoxic for the MRC-5 cells line. Liquid chromatography coupled to tandem mass spectrometry (UPHLC-HRMS/MS) analyses combined with molecular networking data processing were carried out to allow the identification of depsipeptides and cyclopeptides responsible for the cytotoxicity in the dataset. Specific ion clusters from the active Luteibacter sp. extract were also highlighted using an MRSA activity filter. A chemical study of Luteibacter sp. was conducted leading to the structural characterization of eight fatty acid exhibiting antimicrobial activity against MRSA in the tens of μg/mL range.

Structures of topostins, DNA topoisomerase I inhibitors of bacterial origin

The structures of topostins, a novel type of mammalian DNA topoisomerase I inhibitors isolated from the bacterium Flexibacter topostinus sp. nov., have remained unknown. Reexamination of the production of topostins resulted in the isolation of original topostins B (B553 (1) and B567 (2)) and new related compounds named topostins D (D640 (3) and D654 (4)). Their structures, including the absolute stereochemistry, were determined by spectroscopic analyses and chemical degradations. These substances are lipid-containing amino acids and peptides.