M2140
1-Decanoyl-rac-glycerol
≥99%
Sinônimo(s):
Monocaprin
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About This Item
Fórmula empírica (Notação de Hill):
C13H26O4
Número CAS:
Peso molecular:
246.34
Número CE:
Número MDL:
Código UNSPSC:
12352211
ID de substância PubChem:
NACRES:
NA.25
fonte biológica
synthetic (organic)
Ensaio
≥99%
forma
powder
grupo funcional
ketone
tipo de lipídio
neutral glycerides
Condições de expedição
ambient
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
O=C(OCC(O)CO)CCCCCCCCC
InChI
1S/C13H26O4/c1-2-3-4-5-6-7-8-9-13(16)17-11-12(15)10-14/h12,14-15H,2-11H2,1H3
chave InChI
LKUNXBRZDFMZOK-UHFFFAOYSA-N
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Categorias relacionadas
Aplicação
- Novel LC/MS/MS and High-Throughput Mass Spectrometric Assays for Monoacylglycerol Acyltransferase Inhibitors.: This research presents advanced assays for screening inhibitors of monoacylglycerol acyltransferase, with implications for metabolic disease treatment. 1-Decanoyl-rac-glycerol is a key compound in the study (Qi J et al., 2017).
- Optimized reverse micelle surfactant system for high-resolution NMR spectroscopy of encapsulated proteins and nucleic acids dissolved in low viscosity fluids.: The paper describes a novel surfactant system using 1-Decanoyl-rac-glycerol, which improves the NMR spectroscopy of proteins and nucleic acids, offering better resolution and reduced viscosity (Dodevski I et al., 2014).
Ações bioquímicas/fisiológicas
Monocaprin (glycerol monocaprate) is used in the development of antimicrobial disinfectants active against enveloped viruses, and certain yeast and bacteria such as candida albicans and campylobacter.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
Certificados de análise (COA)
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J R Brown et al.
International journal of pharmaceutics, 245(1-2), 133-142 (2002-09-25)
This study explores the potential of the monoglyceride monocaprin as an enhancer of the epithelial permeability of the beta(3)-adrenoceptor agonist BTA-243, as an approach to improving the bioavailability of this drug. The permeabilities of BTA-243 and mannitol (paracellular marker) in
G Bergsson et al.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 109(10), 670-678 (2002-03-14)
The susceptibilities of three Gram-positive cocci to medium-chain saturated and long-chain unsaturated fatty acids and their one-monoglycerides were studied. The bacteria were incubated with equal volumes of lipid solutions for 10 min. Lauric acid, palmitoleic acid and monocaprin reduced the
H Thormar et al.
Letters in applied microbiology, 51(3), 319-324 (2010-07-30)
Contamination in the kitchen with foodborne bacteria is a risk factor in human exposure to these pathogens, an important route being transfer of bacteria from contaminated cutting boards and other surfaces to humans. The aim of this study was to
H Hilmarsson et al.
Poultry science, 85(4), 588-592 (2006-04-18)
Attempts have been made by several workers to prevent or to reduce colonization of Campylobacter in the intestines of broiler chickens by adding antibacterial agents to their food, but the results have varied. Monocaprin, the 1-monoglyceride of capric acid, has
Thórunn O Thorgeirsdóttir et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 59(2), 333-342 (2005-01-22)
The purpose of this study was to characterize the rheological and structural properties of a pharmaceutical multicomponent hydrogel formulation. This formulation consists of a hydrogel-forming poly(acrylic acid) polymer (Carbopol 974P), microbicide (monocaprin), non-ionic surfactant (Tween 20 or Tween 40), and
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