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Merck
CN

58348

SUPELCOSIL LC-18-DB (5 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
NACRES:
NB.21
L × i.d.:
15 cm × 4.6 mm
Particle size:
5 μm
Matrix active group:
C18 (octadecyl) phase
Pore size:
120 Å
Matrix:
silica gel, spherical particle platform
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产品名称

SUPELCOSIL LC-18-DB HPLC 色谱柱, 5 μm particle size, L × I.D. 15 cm × 4.6 mm

agency

suitable for USP L1

feature

endcapped

manufacturer/tradename

SUPELCOSIL

extent of labeling

11.0% Carbon loading

parameter

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

technique(s)

HPLC: suitable

L × I.D.

15 cm × 4.6 mm

surface area

170 m2/g

surface coverage

surface coverage 3.1 μmol/m2

matrix

silica gel, spherical particle platform

matrix active group

C18 (octadecyl) phase

particle size

5 μm

pore size

120 Å

application(s)

food and beverages

separation technique

reversed phase

Quality Level

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Application

SUPELCOSIL LC-18-DB HPLC 色谱柱已用于分离
  • 分析过程中采用 LC 联合主成分分析 (PCA) 的药物相关分析物。
  • 使用 HPLC 结合紫外 (UV) 检测分析人血浆中的氯雷他定。

General description

SUPELCOSIL LC- DB 类的键合相针对碱性化合物进行了特殊的去活化处理。与其它 A 型硅胶反相色谱柱相比,分析有机碱时该色谱柱保留时间更短、峰形更好和柱效更高。

Other Notes

发现适用于高效液相色谱液相色谱-质谱分析的理想LiChropur试剂

Legal Information

SUPELCOSIL is a trademark of Sigma-Aldrich Co. LLC

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kunicki PK.
Journal of Chromatography. B, Biomedical Sciences and Applications, 755(1-2), 331-335 (2001)
Chromatographic classification and comparison of commercially available reversed-phase liquid chromatographic columns using principal component analysis
Euerby MR and Petersson P
Journal of Chromatography A, 994(1-2), 13-36 (2003)
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Journal of pharmaceutical and biomedical analysis, 26(4), 637-650 (2001-08-23)
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O Majid et al.
Therapeutic drug monitoring, 23(2), 163-168 (2001-04-11)
Recipients of organ transplants remain particularly dependent on prednisolone as part of their maintenance immunosuppression. Despite this, the pharmacokinetics of prednisolone have never been fully characterized in these patients, and consequently dosing remains empirical. Accurate monitoring of prednisolone, its primary

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