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Merck

58231

Supelco

SUPELCOSIL LC-CN (5 µm) HPLC Columns

L × I.D. 25 cm × 4.6 mm, HPLC Column

别名:

MTO-SUPELCOSIL LC-CN 5μm 25CM×4.6MM HPLC 色谱柱

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About This Item

分類程式碼代碼:
41115700
eCl@ss:
32110501

product name

SUPELCOSIL LC-CN HPLC 柱, 5 μm particle size, L × I.D. 25 cm × 4.6 mm

agency

suitable for USP L10

特點

endcapped

製造商/商標名

SUPELCOSIL

標籤範圍

4% Carbon loading

參數

≤70 °C temp. range
400 bar pressure (5801 psi)

技術

HPLC: suitable

長度 × 內徑

25 cm × 4.6 mm

表面積

170 m2/g

表面覆盖率

surface coverage 3.5 μmol/m2

基質

silica gel, spherical particle platform

基質活性組

cyano phase

粒徑

5 μm

孔徑

120 Å

pH值範圍

2-7.5

應用

food and beverages

分離技術

hydrophilic interaction (HILIC)
normal phase
reversed phase

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相关类别

一般說明

LC-CN 相通常作为硅胶相的替代者,因为它具有键合相的优点(例如快速平衡,以及对于流动相中水分含量的微小变化更不敏感)。然而 LC-CN 柱通常是在反相的流动相条件下运行。

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法律資訊

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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D Paczkowski et al.
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
S Fogli et al.
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
H Kataoka et al.
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
H Kataoka et al.
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

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