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Fórmula empírica (notación de Hill):
C19H38O3
Número CAS:
Peso molecular:
314.50
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352211
EC Number:
205-471-8
MDL number:
Servicio técnico
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Permítanos ayudarleQuality Segment
assay
≥99% (GC)
form
powder
functional group
ester
lipid type
saturated FAs
shipped in
ambient
storage temp.
−20°C
SMILES string
CCCCCCC(O)CCCCCCCCCCC(=O)OC
InChI
1S/C19H38O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h18,20H,3-17H2,1-2H3
InChI key
RVWOWEQKPMPWMQ-UHFFFAOYSA-N
Application
- Chemical Changes of Hydroperoxy-, Epoxy-, Keto- and Hydroxy-Model Lipids under Simulated Gastric Conditions.: This study explores the stability and chemical transformations of hydroxy fatty acids, including Methyl 12-hydroxystearate, under digestive conditions, providing insight into dietary fat metabolism and its implications for nutritional sciences (Marquez-Ruiz et al., 2021).
- Stimulation of nitrogen removal in the rhizosphere of aquatic duckweed by root exudate components.: This research highlights the potential environmental applications of Methyl 12-hydroxystearate, as a standard, in enhancing nitrogen cycling, important for studies on wastewater treatment and ecosystem management (Lu et al., 2014).
- Synthesis and evaluation of antioxidant and antifungal activities of novel ricinoleate-based lipoconjugates of phenolic acids.: This study investigates the synthesis of derivatives of Methyl 12-hydroxystearate for potential use in food preservation and pharmaceutical applications, emphasizing its antioxidant and antifungal properties (Reddy et al., 2012).
Biochem/physiol Actions
Methyl 12-hydroxystearate is a methyl esterified fatty acid used as a reference for the identification and quantification of 12-hydroxystearic acid, a molecular organogelator, found in tissues, membranes, synthetic molecular gels and copolymers.
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Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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