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物料
fused silica
质量水平
Agency
meets requirements for USP G1, G2, and G9
参数
-60-320 °C temperature (isothermal or programmed)
β值
250
df
0.25 μm
技术
gas chromatography (GC): suitable
长度 × 内径
30 m × 0.25 mm
基质活性基团
Bonded; poly(dimethyl siloxane) phase
色谱柱类型
capillary non-polar
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一般描述
应用:该色谱柱被设计用于当需要非极性色谱柱时的传统通用用途应用。分析物将主要会根据沸点而被分离。
USP代码:该色谱柱满足USP G1、G2及G9要求。
固定相:
USP代码:该色谱柱满足USP G1、G2及G9要求。
固定相:
- 键合
- 聚(二甲基硅氧烷)
- ≤0.32 mm内径,<2 μm:-60°C至320°C (等温或程序性的)
- ≤0.32 mm内径,≥2 μm: -60°C至300°C (等温或程序性的)
- ≥0.53 mm内径, <2 μm: -60°C至300°C (等温)或320°C(程序性的)
- ≥0.53 mm内径, ≥2 μm: -60 °C至260 °C (等温)或280 °C(程序性的)
应用
SPB®-1气相毛细管色谱柱可用于通过化学发光检测法对氮化合物(定量)形态分析,该类化合物是极性的并且具有一定程度的碱性。
其他说明
我们提供各种色谱配件,包括 分析注射器
法律信息
SPB is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
214.0 °F - closed cup
闪点(°C)
101.1 °C - closed cup
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An automated static headspace gas chromatographic method for the determination of residual solvents in the bulk drug substance alpha-phenyl-1-(2-phenylethyl)-piperine methanol, a serotonin 5-HT2 receptor antagonist, is evaluated. The method includes the use of 1-propanol as an internal standard. The gas
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A static headspace gas chromatographic method is developed and evaluated for the quantitation of residual 2-propanol, methanol, and toluene in bulk (2alpha, 6alpha, 8alpha, 9alpha beta)-octahydro-3-oxo-2,6-methanon-2H-quinolizin-8-yl-1H-indole-3-caboxylate methanesufonate hydrate, a serotonin 5-HT3 receptor antagonist drug compound. This method is accurate and
The Analyst, 117(7), 1111-1127 (1992-07-01)
Headspace gas chromatography with split flame-ionization-electron-capture detection is a simple method of screening for a wide range of volatile substances in biological fluids. A 60 m x 0.53 mm i.d. thick-film (5 microns) fused-silica capillary coated with SPB-1 (Supelchem) with
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In this study, a promising bioremediation approach was developed to remove [Co(III)-EDTA](-) complex that is generated during the waste management process. Though several studies have been reported on bioremediation of cobalt, the removal of [Co(III)-EDTA](-) complex has not been tested.
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The four possible isomers of tetradeca-4,8-dien-1-yl acetate and corresponding alcohols were synthesized stereoselectively by synthetic routes employing Wittig coupling reaction for the preparation of (Z,E)- and (Z,Z)-isomers, and alkylation of terminal alkynes for the preparation of (E,E)- and (E,Z)-isomers as
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