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Merck
CN

T9900

Methyl tricosanoate

≥99.0% (GC)

Synonym(s):

Tricosanoic acid methyl ester

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About This Item

Linear Formula:
CH3(CH2)21COOCH3
CAS Number:
2433-97-8
Molecular Weight:
368.64
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24900613
EC Number:
219-420-2
Beilstein/REAXYS Number:
1796627
MDL number:
MFCD00009349

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InChI

1S/C24H48O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26-2/h3-23H2,1-2H3

InChI key

VORKGRIRMPBCCZ-UHFFFAOYSA-N

SMILES string

CCCCCCCCCCCCCCCCCCCCCCC(=O)OC

biological source

synthetic (organic)

assay

≥99.0% (GC)

form

powder

technique(s)

gas chromatography (GC): suitable

color

white

Quality Level

200

solubility

chloroform: 50 mg/mL, clear, colorless

application(s)

agriculture
general analytical

functional group

ester

lipid type

saturated FAs

shipped in

ambient

storage temp.

2-8°C

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General description

Methyl tricosanoate, also recognized as Tricosanoic acid methyl ester, represents the fatty acid methyl ester (FAME) form of tricosanoic acid. This odd-numbered long-chain fatty acid methyl ester is atypical in many biological systems, making it valuable as a biomarker. Tricosanoic acid is naturally synthesized in certain plants and mammals, including humans, where it predominates as a skin lipid. It can be found acylated to various glyco-, phospho-, and sphingolipids, including gangliosides. This fatty acid holds significance in biochemical, lipidomics, and metabolomics research applications.

Application

Methyl tricosanoate has been used as an internal standard to quantify fatty acids or fatty acid methyl esters (FAMEs).

Features and Benefits

  • High-quality molecule suitable for mulitple research applications
  • Commonly employed in Metabolomics and Biochemical studies

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113.00 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
0000534934
0000534933
0000528462
0000528462
0000534934

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Carolina Oliveira de Souza et al.
Lipids in health and disease, 16(1), 78-78 (2017-04-16)
Palm olein is used in infant formula fat blends in order to match the fatty acid profile of human milk. While the effects on fatty acid balance have been evaluated, the use of palm olein in combination with palm kernel
Daniel L Forwood et al.
Meat science, 173, 108402-108402 (2020-12-15)
This study investigated the effect of feeding unsaleable carrots to lambs within a total-mixed ration (TMR) on performance, carcass characteristics, meat quality and sensory parameters. Thirty-six Australian Merino wether lambs were fed a control (barley-based) or carrot-based TMR for 11-weeks.
Marine Vallet et al.
Marine drugs, 18(8) (2020-07-28)
Kelps are colonized by a wide range of microbial symbionts. Among them, endophytic fungi remain poorly studied, but recent studies evidenced yet their high diversity and their central role in algal defense against various pathogens. Thus, studying the metabolic expressions
K E Aarak et al.
Food & function, 5(9), 2331-2337 (2014-08-01)
The aim of the present work was to study the effect of a broccoli phytochemical extract (Br-ex) on the release of fatty acids (FA) from salmon muscle (SM) and salmon oil (SO) during in vitro digestion. The hypothesis of the
Lihong Zhou et al.
Journal of proteome research, 14(5), 2331-2347 (2015-04-01)
Silkworm (Bombyx mori) is a lepidopteran-holometabolic model organism. To understand its developmental biochemistry, we characterized the larval hemolymph metabonome from the third instar to prepupa stage using (1)H NMR spectroscopy whilst hemolymph fatty acid composition using GC-FID/MS. We unambiguously assigned
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