跳转至内容
Merck
CN

880341P

Avanti

16:0-16:0 (16-F) PC

Avanti Research - A Croda Brand

别名:

1-palmitoyl-2-(16-fluoropalmitoyl)-sn-glycero-3-phosphocholine

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C40H79NO8PF
化学文摘社编号:
分子量:
752.03
UNSPSC代码:
12352211
NACRES:
NA.25
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

16:0-16:0 (16-F) PC, Avanti Research - A Croda Brand 880341P, powder

方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 10 mg (880341P-10mg)
pkg of 1 × 25 mg (880341P-25mg)

制造商/商品名称

Avanti Research - A Croda Brand 880341P

运输

dry ice

储存温度

−20°C

SMILES字符串

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCCCCCCCCCC([H])([H])F)=O)COC(CCCCCCCCCCCCCCC)=O)=O

一般描述

16:0-16:0 (16-F) PC or 1-palmitoyl-2-(16-fluoropalmitoyl)-sn-glycero-3-phosphocholine is a monofluorinated analog of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC).

应用

16:0-16:0 (16-F) PC or 1-palmitoyl-2-(16-fluoropalmitoyl)-sn-glycero-3-phosphocholine is suitable for use as a rotational-echo double-resonance (REDOR) probe to analyze peptides integrated into phospholipid bilayers.

生化/生理作用

Fluorinated lipids act as drug carriers. They aid in characterizing proteins and membranes. 16:0-16:0 (16-F) PC or 1-palmitoyl-2-(16-fluoropalmitoyl)-sn-glycero-3-phosphocholine automatically interdigitates lipid bilayers without inducing agents. This is due to its hydrophilic nature because of the presence of highly polar C-F bond at the terminal end of the sn-2 acyl chain.

包装

5 mL Amber Glass Screw Cap Vial (880341P-10mg)
5 mL Amber Glass Screw Cap Vial (880341P-25mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

WGK

WGK 3

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

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

Babak Sanii et al.
The journal of physical chemistry. B, 114(1), 215-219 (2009-12-17)
In free bilayers, the fluid to gel main phase transition of a monofluorinated phospholipid (F-DPPC) transforms a disordered fluid bilayer into a fully interdigitated monolayer consisting of ordered acyl tails. This transformation results in an increase in molecular area and
Syed W H Shah et al.
Chemistry and physics of lipids, 230, 104918-104918 (2020-05-18)
The monolayer behavior of a l-DPPC derivative with a single fluorination in one of its terminal methyl groups (F-DPPC) at air-water interface was investigated by epifluorescence microscopy and infrared reflection absorption spectroscopy (IRRAS). Epifluorescence microscopy was utilized to study the
D J Hirsh et al.
Biophysical journal, 75(4), 1858-1868 (1998-09-24)
16-Fluoropalmitic acid was synthesized from 16-hydroxypalmitic acid using diethylaminosulfur trifluoride. This monofluorinated fatty acid then was used to make 1-palmitoyl-2-[16-fluoropalmitoyl]-phosphatidylcholine (F-DPPC) as a fluorinated analog of dipalmitoylphosphatidylcholine (DPPC). Surprisingly, we found that the phase transition temperature (Tm) of F-DPPC occurs
Eric A Smith et al.
Chemistry and physics of lipids, 165(2), 151-159 (2011-12-28)
Unlike the parent phospholipid, 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), the monofluorinated analog, 1-palmitoyl-2-(16-fluoropalmitoyl)sn-glycero-3-phosphocholine (F-DPPC), spontaneously forms an interdigitated gel phase (L(β)I) below the main transition temperature (T(m)). We have examined the effects of introducing cholesterol to F-DPPC and 1:1 F-DPPC/DPPC membranes using a
Eric A Smith et al.
Biophysical chemistry, 147(1-2), 20-27 (2010-01-13)
In aqueous solution, the monofluorinated phospholipid 1-palmitoyl-2-[16-fluoropalmitoyl]sn-glycero-3-phosphocholine (F-DPPC) interdigitates without the use of inducing agents. To understand the thermal and physical properties of this unique lipid, F-DPPC was combined with the non-fluorinated 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), and 1,2-diarachidoyl-sn-glycero-3-phosphocholine (DAPC). Differential scanning calorimetry

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.

联系客户支持