點擊放大甲醇中4種β-受體激動劑混標
This certificate is designed in accordance with ISO 17034 and ISO Guide 31. This reference material (RM) was designed,produced and verified in accordance with ISO/IEC 17025, ISO 17034 and a registered quality management system ISO 9001.
(-18±5)℃冷凍，置于陰涼處
| CERTIFIED | |||||
| Component No. (組分數) | Peak Sequence (出峰順序) | Component (組分) | CAS No. | Concentration (μg/mL) (濃度) | Relative Expanded Uncertainty(%) (k=2) (相對擴展不確定度) |
| 1 | 1 | Salbutamol (沙丁an醇) | 18559-94-9 | 100 | 3 |
| 2 | 2 | Cimaterol (西馬te羅) | 54239-37-1 | 100 | 3 |
| 3 | 3 | Ractopamine Hydrochloride1 (鹽酸萊ke多巴胺) | 90274-24-1 | 100(free base) | 3 |
| 4 | 4 | Clenbuterol Hydrochloride1 (鹽酸克lun特羅) | 21898-19-1 | 100(free base) | 3 |
A:Acetonitrile(乙腈)
B:0.1%Phosphoric Acid(0.1%磷酸)
| Time/min | A/% | B/% |
| 0.30 | 5 | 95 |
| 5.00 | 70 | 30 |
| 7.50 | 70 | 30 |
| 8.50 | 85 | 15 |
| 9.00 | 85 | 15 |
| 9.01 | 5 | 95 |
| 11.00 | 5 | 95 |
Note
This RM is intended for use in a laboratory as a calibration and quality control standard or in method development for analytical techniques.
The certified value(s) and uncertainty(ies) are determined in accordance with ISO 17034 with an 95% confidence level (k=2). Uncertainty is based on the Total Combined Uncertainty, including uncertainties of preparation, purity of neat materials, homogeneity, stability testing.
The balances used for gravimetric measurements are calibrated with weights traceable to the national standards. The calibration of the balances is verified annually by an external accredited calibration service. This analysis method has been verified using an approach consistent with ISO 17034:2016 & ISO 17025:2017.
Random replicate samples of the final packaged RM have been analysed to prove homogeneity consistent with ISO 17034.
The RM should be stored in the original sealed bottle at the indicated temperature.
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