product name
SUPELCOSIL™ LC-CN HPLC 柱, 3 μm particle size, L × I.D. 7.5 cm × 3 mm
物料
stainless steel column
质量水平
Agency
suitable for USP L10
产品线
SUPELCOSIL™
特点
endcapped
制造商/商品名称
SUPELCOSIL™
包装
1 ea of
标记范围
4% Carbon loading
参数
≤70 °C temp. range
400 bar pressure (5801 psi)
技术
HPLC: suitable
长度 × 内径
7.5 cm × 3 mm
表面积
170 m2/g
表面覆盖度
surface coverage 3.5 μmol/m2
基质
silica gel, spherical particle platform
fully porous particle
基质活性基团
cyano phase
粒径
3 μm
孔径
120 Å
pH值范围
2-7.5
应用
food and beverages
分离技术
hydrophilic interaction (HILIC)
normal phase
reversed phase
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法规信息
新产品
Polish journal of pharmacology, 47(5), 429-434 (1995-09-01)
This paper describes a simple high-performance liquid chromatographic (HPLC) method for the determination of diltiazem and desacetyldiltiazem in human serum. After basic methyl-tert-butyl ether extraction and back-extraction with hydrochloric acid, the drug and its metabolite was injected into a Supelcosil
Therapeutic drug monitoring, 21(3), 367-375 (1999-06-12)
A single high-performance liquid chromatography (HPLC) method, suitable for the analysis of daunorubicin, idarubicin, doxorubicin, epirubicin, and their 13-dihydro metabolites is validated in the present study. Preparation of plasma samples was performed by a first extraction of analytes with a
Journal of analytical toxicology, 24(4), 257-265 (2000-06-29)
A simple and rapid method for the determination of amphetamine, methamphetamine, and their 3,4-methylenedioxy derivatives in urine samples was developed using automated in-tube solid-phase microextraction (SPME) coupled with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS). In-tube SPME is an extraction technique
Journal of chromatography. B, Biomedical sciences and applications, 731(2), 353-359 (1999-10-08)
The technique of automated in-tube solid-phase microextraction (SPME) coupled with liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS) was evaluated for the determination of ranitidine. In-tube SPME is an extraction technique for organic compounds in aqueous samples, in which analytes are extracted
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