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フォーム
liquid
包装
pkg of 1 × 10 mg (861809O-10mg)
pkg of 1 × 100 mg (861809O-100mg)
メーカー/製品名
Avanti Research™ - A Croda Brand
輸送温度
dry ice
保管温度
−20°C
関連するカテゴリー
詳細
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.
アプリケーション
Oleic acid-d9 has been used for spiking Alexidine treatment media during preparation of sample for liquid chromatography-mass spectrometry (LC-MS) analysis.
包装
5 mL Clear Glass Sealed Ampule (861809O-100mg)
5 mL Clear Glass Sealed Ampule (861809O-10mg)
法的情報
Avanti Research is a trademark of Avanti Polar Lipids, LLC
保管分類コード
10 - Combustible liquids
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
861809O-10MG:
861809O-100MG:
861809O-BULK:
861809O-VAR:
最新バージョンのいずれかを選択してください:
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High-content screen for modifiers of Niemann-Pick type C disease in patient cells
Pugach EK, et al.
Human Molecular Genetics, 27(12), 2101-2112 (2018)
Tamim A Darwish et al.
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
Darwish TA, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 56(9-10), 520-529 (2013)
Siddabasave Gowda B Gowda et al.
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
Emily K Pugach et al.
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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