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HomeSolid Phase Extraction (SPE)Solid Phase Extraction: Normal Phase Methodology

Solid Phase Extraction: Normal Phase Methodology

Non-polar Sample Matrix/ Mobile Phase Environment

In order for polar retention to occur between the sorbent and the sample, the analyte must be introduced to the SPE device in a non-polar sample or mobile phase environment. Therefore, typical sample matrices that can be employed in normal-phase SPE include hydrocarbon or fatty oils diluted in an organic solvent, hexane, isooctane, chlorinated solvents, THF, diethyl ether, and ethyl acetate.

Most organic analytes exhibit some polar functionalities that can be exploited for normal-phase separation. Because many molecules exhibit polar functionality, each interaction can provide different levels of selectivity offering highly selective separations of compounds very similar in structure.

Normal-Phase SPE
Retention MechanismPolar Interactions
  • Hydrogen bonding, π-π, dipole-dipole, and induced dipole-dipole
Sample MatrixNon-polar samples
  • Organic extracts of solids
  • Very non-polar solvents
  • Fatty oils, hydrocarbons
Analyte CharacteristicsAnalytes exhibiting polar functionalities
  • Hydroxyl groups, carbonyls, amines, double bonds
  • Hetero atoms (O, N, S, P)
  • Functional groups with resonance properties
Elution SchemePolar interactions disrupted with a more polar solvent or solution
  • Acetonitrile, methanol, isopropanol
  • Combinations of buffer/solvent or solvent/solvent mixtures
Common Applications
  • Cleanup of organic extracts of soils and sludge
  • Fractionation of petroleum hydrocarbons
  • PCBs in transformer oil
  • Isolation of compounds in cosmetics

Basic Steps

  1. Sample Pre-treatment Liquid samples should be initially extracted or diluted with a non-polar solvent such as hexane or a chlorinated solvent. Soil, sediment, and other solid samples are initially extracted (Soxhlet or sonication) with a non-polar solvent, and concentrated prior to SPE cleanup. Aqueous residues in the sample can reduce normal-phase retention. It may be necessary to further dry the organic extract with sodium sulfate or magnesium sulfate prior to SPE.

  2. Conditioning/Equilibration Condition and equilibriate with 2-3 tube volumes of a non-polar solvent similar or identical to sample matrix resulting from sample pre-treatment.

  3. Sample Load Apply sample (from step 1) at a consistent and reduced flow rate of ~1-2 drops/second to ensure optimal retention. The compounds should be a non-polar solvent (e.g., hexane) for optimal retention. Note that methanol and acetonitrile are often used as elution solvents in normal-phase SPE, and will often not promote compound retention during sample load.

  4. Wash Sample interferences are often co-retained with compounds of interest during sample load. A wash step is necessary to elute interferences without prematurely eluting compounds of interest. In normal-phase SPE, 1-2 tube volumes of the solvent used in sample pre-treatment and conditioning can be used during wash.

  5. Elution Disrupt polar interactions with a solvent or solvent/buffer mixture more polar than both the sample and wash solutions. Typical elution solvents include water miscible organic solvents such as acetone, acetonitrile, methanol, and isopropanol. Eluting with increasingly polar solvents (or solvent mixtures) in succession can also fractionate multiple compound classes. See “Common Normal-Phase Solvents” table for assistance.

  6. Eluate Post-treatment Normal-phase SPE is often followed by GC analysis, and therefore requires a volatile sample matrix prior to injection. Use sodium sulfate or magnesium sample to remove residual moisture. Further SPE eluate concentration may also be necessary prior to analysis.

Common Normal-Phase Solvents

SolventElutropic (e°) or
elution strength
on silica
Promotes
Normal-Phase
Retention / Elution
Hexane0.00Retention
Isooctane0.00
Carbon tetrachloride0.14
Toluene0.22
Benzene0.27
Tert-butyl methyl ether0.29
Chloroform0.31
Methylene chloride (dichloromethane)0.32
Diethyl ether0.29
Ethyl acetate0.43
Tetrahydrofuran0.35
Acetone0.45
Acetonitrile0.50
40% methanol in acetonitrile0.67
20% methanol in diethyl ether0.65
20% methanol in methylene chloride0.63
Isopropanol0.63
Methanol0.73
Water>0.73Elution
Acetic acid>0.73
Materials
产品编号产品名称说明价格
MSQC16SILuLite SigmaMAb Adalimumab Monoclonal Antibodyrecombinant, expressed in CHO cells
31417葡聚糖 来源于肠系膜明串珠菌analytical standard, Mw 5,000
I4506IgG 来源于人类血清reagent grade, ≥95% (SDS-PAGE), essentially salt-free, lyophilized powder
50933盐酸胍 盐酸盐BioUltra, ≥99.5% (AT)
09830碳酸氢铵BioUltra, ≥99.5% (T)
F8435糖苷酶F 来源于脑膜脓毒性伊丽莎白菌lyophilized powder, recombinant, expressed in E. coli
EMS0011Low-Artifact Digestion BufferMinimizes artifactual deamidation and oxidation during trypsin digestion prior to peptide mapping
MRCF0R030Microcon®离心超滤管NMWCO 30 kDa, Ultracel® regenerated cellulose membrane (low binding), sample volume 0.5 mL
156159氰基硼氢化钠reagent grade, 95%
PHR1252普鲁卡因胺 盐酸盐Pharmaceutical Secondary Standard; Certified Reference Material
D8418二甲基亚砜
695092乙酸glacial, ACS reagent, ≥99.7%
55465-UDiscovery® Glycan SPE Tubebed wt. 50 mg, volume 1 mL, pk of 108
1.00029乙腈hypergrade for LC-MS LiChrosolv®
VM20VM20真空歧管For processing up to 20 plasmid purification samples simultaneously
50994-UBIOshell Glycan HPLC ColumnsL × I.D. 15 cm × 2.1 mm, 2.7 μm particle size
1.00029乙腈hypergrade for LC-MS LiChrosolv®
70221甲酸铵eluent additive for LC-MS, LiChropur, ≥99.0%
5.33002甲酸98%-100%for LC-MS LiChropur
ZIQ7000T0CMilli-Q® IQ 7000 超纯水净化系统output: type 1 water (18.2 MΩ·cm), the most advanced Milli-Q® ultrapure (Type 1) water purification system that is intelligent, intuitive, and green.
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