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Merck
CN

F9005

Supelco

氟芬那酸

analytical standard, for drug analysis

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别名:
N-(3-[三氟甲基]苯基)邻氨基苯甲酸, N-(α,α,α-三氟-间甲苯基)邻氨基苯甲酸
线性分子式:
2-(CF3C6H4NH)C6H4CO2H
CAS号:
分子量:
281.23
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard, for drug analysis

质量水平

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

132-135 °C (lit.)

应用

forensics and toxicology
pharmaceutical (small molecule)
veterinary

格式

neat

SMILES字符串

OC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F

InChI

1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)

InChI key

LPEPZBJOKDYZAD-UHFFFAOYSA-N

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一般描述

氟芬那酸是一种非甾体抗炎药,可作为一种有效的止痛剂。

应用

有关合适仪器技术的更多信息,请参考产品分析证书。如需进一步支持,请联系技术服务部门。
氟芬那酸已被用作使用固态密度泛函理论和太赫兹光谱学研究氟芬那酸的两种明确多晶型(如 I 型和 III 型)的标准品。

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


分析证书(COA)

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Conformational origins of polymorphism in two forms of flufenamic acid
Delaney P S, et al.
Journal of Molecular Structure, 1078, 83-89 (2014)
Julia C Schwarz et al.
International journal of pharmaceutics, 437(1-2), 83-88 (2012-08-21)
Nanocarriers are highly interesting delivery systems for the dermal application of drugs. Based on a eudermic alkylpolyglycosid nanoemulsions, solid lipid nanoparticles (SLN) and nano-structured lipid carriers (NLC) were prepared by ultrasonic dispersion. The ultrasound preparation technique turned out to be
Antonella Di Pizio et al.
Cellular and molecular life sciences : CMLS, 77(3), 531-542 (2019-06-27)
Human bitter taste receptors (TAS2Rs) are a subfamily of 25 G protein-coupled receptors that mediate bitter taste perception. TAS2R14 is the most broadly tuned bitter taste receptor, recognizing a range of chemically diverse agonists with micromolar-range potency. The receptor is
Minsoo Kim et al.
Pharmaceutics, 11(3) (2019-03-22)
Concomitant use of rivaroxaban with non-dihydropyridine calcium channel blockers (non-DHPs) might lead to an increase of systemic rivaroxaban exposure and anticoagulant effects in relation to the inhibition of metabolic enzymes and/or transporters by non-DHPs. This study was designed to evaluate
Jon Andoni Sánchez et al.
Immunobiology, 222(2), 241-250 (2016-10-11)
Previous works with autumnalamide reported that Store Operated Calcium (SOC) channels were blocked through mitochondrial modulation. In the present paper we studied the effect of autumnalamide on ionomycin Ca2+ fluxes. Thus, autumnalamide did not modify ionomycin-sensitive intracellular pools while the

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