atenolol-d7, R/S(±)-chlorpheniramine-d6, and R/S(±)-citalopram-d6. All chemicals were purchased as Methanolic solutions of 0.1 mg mL -1 or 1 mg mL -1 , or as powder. Powders were prepared at an appropriate concentration in Methanol. All solutions were stored in the dark at -20°C. Oasis HLB cartridges (3cc 60mg) were purchased from Waters (Manchester, UK).
R s salbutamol
R/S(±)-salbutamol is a racemic mixture of two enantiomers, R-salbutamol and S-salbutamol. It is a synthetic compound used as a reference standard in analytical and research applications.
Lab products found in correlation
3 protocols using r s salbutamol
Chiral Separation and Quantification Protocol
atenolol-d7, R/S(±)-chlorpheniramine-d6, and R/S(±)-citalopram-d6. All chemicals were purchased as Methanolic solutions of 0.1 mg mL -1 or 1 mg mL -1 , or as powder. Powders were prepared at an appropriate concentration in Methanol. All solutions were stored in the dark at -20°C. Oasis HLB cartridges (3cc 60mg) were purchased from Waters (Manchester, UK).
Multi-analyte LC-MS/MS Analysis of Environmental Samples
propranolol-d7 and R/S(±)-salbutamol-d3. Oasis HLB (60mg, 3mL) cartridges for solid phase extraction (SPE) were obtained from Waters (Manchester, UK). HPLC-grade methanol, ammonium acetate and acetic acid were purchased from Fisher Scientific (Loughborough, UK). Ultra-pure water used throughout the study was of 18.2 MΩ cm -1 quality. For method development and validation, effluent (5 L) was collected from a septic tank which serves 7 inhabitants in Aberdeenshire, North East Scotland. Stream water (10 L) was collected from a tributary of the River Don, Aberdeenshire.
Chiral Analysis of Pharmaceutical Residues
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