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Merck
CN

59137

SUPELCOSIL LC-DABS (3 µm) HPLC Columns

L × I.D. 15 cm × 4.6 mm, HPLC Column

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关于此项目

UNSPSC Code:
41115700
eCl@ss:
32110501
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产品名称

SUPELCOSIL LC-DABS HPLC 色谱柱, 3 μm particle size, L × I.D. 15 cm × 4.6 mm

manufacturer/tradename

SUPELCOSIL

extent of labeling

12.3% carbon loading

parameter

0-70 °C temperature, 400 bar pressure (5801 psi)

technique(s)

HPLC: suitable

L × I.D.

15 cm × 4.6 mm

matrix

silica gel, high purity, spherical particle platform

matrix active group

C18 (octadecyl) phase

particle size

3 μm

pore size

120 Å

application(s)

food and beverages

compatibility

for use with Dabsyl-AA

separation technique

reversed phase

General description

SUPELCOSIL LC-DABS 色谱柱的特色是一种经过特殊处理和测试的十八烷基硅烷键合相,用于柱前衍生丹磺酰氨基酸的反相分离。在一小时内可以分离超过 30 种氨基酸。

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC




历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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实验方案

氨基酸分析是精确测定蛋白质量的合适工具,但也提供有关相对氨基的详细信息。

Amino Acid Analysis is the suitable tool for precise determination of protein quantities but also provides detailed information regarding the relative amino.


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Toxicology mechanisms and methods, 25(5), 410-416 (2015-05-30)
We have developed a simple, reversed-phase high-performance liquid chromatography (RP-HPLC) method for the determination of bisphenol A (BPA) in thermal paper cash register receipts (CRs). The method is suitable for analysis of other types of bisphenols and it involves an
R Herráez-Hernández et al.
Journal of chromatographic science, 35(4), 169-175 (1997-04-01)
A chromatographic method for the analysis of amphetamine and related compounds in urine using 3,5-dinitrobenzoyl chloride (3,5-DNB) as a labeling reagent is presented. This assay is based on the employment of solid-phase extraction (SPE) cartridges for sample cleanup and derivatization.
Vijay V Upreti et al.
Biomedical chromatography : BMC, 17(6), 385-390 (2003-09-19)
A simple and sensitive high-performance liquid chromatography (HPLC) method has been developed and validated for the determination of DRF-1042, a novel orally active camptothecin (CPT) analog, in human plasma. The sample preparation was a simple deproteinization with acidified methanol yielding