跳转至内容
Merck
CN
所有图片(1)

主要文件

安全信息

861809O

Avanti

油酸-d9

Avanti Research - A Croda Brand

别名:

(15,15,16,16,17,17,18,18,18-d9)油酸

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C18H25D9O2
分子量:
291.52
MDL编号:
UNSPSC代码:
12352100
NACRES:
NA.25

表单

liquid

包装

pkg of 1 × 10 mg (861809O-10mg)
pkg of 1 × 100 mg (861809O-100mg)

制造商/商品名称

Avanti Research - A Croda Brand

运输

dry ice

储存温度

−20°C

一般描述

油酸-d9是油酸的氘代衍生物。油酸对于细胞膜的结构和功能很重要。它广泛用于核磁共振、红外、质谱和中子散射研究。

应用

在制备用于液相色谱-质谱(LC-MS)分析的样品期间,油酸-d9已用于加标阿来西定治疗培养基。

包装

5 mL透明玻璃密封安瓿(861809O-100mg)
5 mL透明玻璃密封安瓿(861809O-10mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

10 - Combustible liquids

法规信息

美国出口管控1C298产品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

抱歉,我们目前尚未线上提供该产品的COA。

如需帮助,请联系 客户支持

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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)
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
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)
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

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门