861809O
Avanti
oleic acid-d9
Avanti Research™ - A Croda Brand
Synonyme(s) :
(15,15,16,16,17,17,18,18,18-d9)oleic acid
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About This Item
Produits recommandés
Forme
liquid
Conditionnement
pkg of 1 × 10 mg (861809O-10mg)
pkg of 1 × 100 mg (861809O-100mg)
Fabricant/nom de marque
Avanti Research™ - A Croda Brand
Conditions d'expédition
dry ice
Température de stockage
−20°C
Catégories apparentées
Description générale
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.
Application
Oleic acid-d9 has been used for spiking Alexidine treatment media during preparation of sample for liquid chromatography-mass spectrometry (LC-MS) analysis.
Conditionnement
5 mL Clear Glass Sealed Ampule (861809O-100mg)
5 mL Clear Glass Sealed Ampule (861809O-10mg)
Informations légales
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Code de la classe de stockage
10 - Combustible liquids
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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)
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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
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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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