| ExperimentID | EXA000323 |
|---|---|
| ChemicalID | CH0000272 |
| Chemical Name | Clarithromycin |
| Official Method | No |
| Chromatography | LC |
| Chromatography mfr. | [1]ACQUITY UPLC, Waters; [2]1260, Agilent |
| Column | Atiantis T3 150 mm x 2.1 mm, 3 μm |
| Column mfr. | Waters |
| Detector | MS/MS |
| Detector mfr. | [1]Xevo TQ, Waters; [2]QTRAP 4500; AB Sciex |
| Ionization | SRM-ESI-positive |
| Extraction | SPE |
| Extraction Details | Oass HLB Plus 225 mg Short 10 mL/min; Eluted with Methanol |
| Clean-up 1st | Filtration |
| Clean-up 1st Details | Filtered with LH filter 0.45 μm; Hydrophilic PTFE 13 mm, Millex |
| Clean-up 2nd | |
| Clean-up 2nd Details | |
| Clean-up Spike | |
| Syringe Spike | |
| Derivatization | |
| Recovery Correction | |
| Instrument Detection Limit | |
| Instrument Quantification Limit | |
| Method Detection Limit | 1.4 ng/L |
| Method Quantification Limit | |
| Repeatability | |
| Standard | |
| Recovery (CRM) | |
| Recovery (spiked) | |
| Recovery (IS) | |
| Protocol | https://www.env.go.jp/chemi/kurohon/2020/shosai/5_2_2.pdf |
| Remarks | Analysis method: p.3 |
| RegisterDate | 2022/5/06 |
| UpdateDate | 2022/5/06 |