M7531
11-Methyllauric acid
≥98%
Synonym(s):
11-Methyldodecanoic acid, Isotridecanoic acid
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About This Item
Empirical Formula (Hill Notation):
C13H26O2
CAS Number:
Molecular Weight:
214.34
UNSPSC Code:
12352211
PubChem Substance ID:
MDL number:
InChI
1S/C13H26O2/c1-12(2)10-8-6-4-3-5-7-9-11-13(14)15/h12H,3-11H2,1-2H3,(H,14,15)
SMILES string
CC(C)CCCCCCCCCC(O)=O
InChI key
SIOLDWZBFABPJU-UHFFFAOYSA-N
assay
≥98%
form
powder
functional group
carboxylic acid
lipid type
saturated FAs
shipped in
ambient
storage temp.
−20°C
Biochem/physiol Actions
11-Methyl-lauric (11-Methyldodecanoic) acid is a methylated 13-carbon analog of the 12-carbon chain saturated fatty acid lauric acid. 11-Methyllauric may be used in comparative studies of the ability of medium chain saturated fatty acids to modulate inflammatory processes and to enhance skin permeation (drug delivery) formulations.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Sunita Gupta et al.
Journal of neurochemistry, 120(6), 1060-1071 (2012-01-18)
This study describes the effects of long-chain fatty acids on inflammatory signaling in cultured astrocytes. Data show that the saturated fatty acid palmitic acid, as well as lauric acid and stearic acid, trigger the release of TNFα and IL-6 from
Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin.
Hossain MA, Ahmed SU, Plakogiannis FM.
Drug Devel. Ind. Pharm., 38, 323-330 (2012)
Eric Soupene et al.
Scientific reports, 7(1), 15767-15767 (2017-11-19)
De novo lipid synthesis and scavenging of fatty acids (FA) are processes essential for the formation of the membrane of the human pathogen Chlamydia trachomatis (C.t.). Host FA are assimilated via esterification by the bacterial acyl-acyl carrier protein (ACP) synthase
Yosuke Toyotake et al.
Biochemical and biophysical research communications, 500(3), 704-709 (2018-04-22)
1-Acyl-sn-glycerol-3-phosphate O-acyltransferase (PlsC) plays an essential role in the formation of phosphatidic acid, a precursor of various membrane phospholipids (PLs), in bacteria by catalyzing the introduction of an acyl group into the sn-2 position of lysophosphatidic acid. Various bacteria produce
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