861809O
Avanti
oleic acid-d9
Avanti Research™ - A Croda Brand
Synonym(e):
(15,15,16,16,17,17,18,18,18-d9)oleic acid
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About This Item
Empfohlene Produkte
Form
liquid
Verpackung
pkg of 1 × 10 mg (861809O-10mg)
pkg of 1 × 100 mg (861809O-100mg)
Hersteller/Markenname
Avanti Research™ - A Croda Brand
Versandbedingung
dry ice
Lagertemp.
−20°C
Verwandte Kategorien
Allgemeine Beschreibung
Oleic acid-d9 is a deuterated derivative of oleic acid. Oleic acid is important for structure and function of cellular membranes. It is widely used in nuclear magnetic resonance, infrared, mass spectroscopy and neutron scattering studies.
Anwendung
Oleic acid-d9 has been used for spiking Alexidine treatment media during preparation of sample for liquid chromatography-mass spectrometry (LC-MS) analysis.
Verpackung
5 mL Clear Glass Sealed Ampule (861809O-100mg)
5 mL Clear Glass Sealed Ampule (861809O-10mg)
Rechtliche Hinweise
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Lagerklassenschlüssel
10 - Combustible liquids
Analysenzertifikate (COA)
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Journal of labelled compounds & radiopharmaceuticals, 56(9-10), 520-529 (2013-11-29)
Oleic acid and its phospholipid derivatives are fundamental to the structure and function of cellular membranes. As a result, there has been increasing interest in the availability of their deuterated forms for many nuclear magnetic resonance, infrared, mass spectroscopy and
Synthesis of deuterated [D32] oleic acid and its phospholipid derivative [D64] dioleoyl-sn-glycero-3-phosphocholine
Journal of Labelled Compounds & Radiopharmaceuticals, 56(9-10), 520-529 (2013)
High-content screen for modifiers of Niemann-Pick type C disease in patient cells
Human Molecular Genetics, 27(12), 2101-2112 (2018)
Rapid communications in mass spectrometry : RCM, 34(17), e8831-e8831 (2020-05-18)
Fatty acid esters of hydroxy fatty acids (FAHFAs) are recently discovered endogenous lipids with outstanding health benefits. FAHFAs are known to exhibit antioxidant, antidiabetic and anti-inflammatory properties. The number of known long-chain FAHFAs in mammalian tissues and dietary resources increased
Human molecular genetics, 27(12), 2101-2112 (2018-04-17)
Niemann-Pick type C (NPC) disease is a rare lysosomal storage disease caused primarily by mutations in NPC1. NPC1 encodes the lysosomal cholesterol transport protein NPC1. The most common NPC1 mutation is a missense mutation (NPC1I1061T) that causes misfolding and rapid
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