组分信息
| CAS号 | 名称 | 标准值 | 单位 |
|---|---|---|---|
| 26787-78-0 | 阿莫西林 | ≥95 | % |
| 69-53-4 | 氨苄西林 | ≥95 | % |
| 113-98-4 | 青霉素G钾 | ≥95 | % |
| 87-08-1 | 青霉素V | ≥95 | % |
| 1173-88-2 | 苯唑西林钠 | ≥95 | % |
| 7081-44-9 | 氯唑西林钠一水合物 | ≥95 | % |
| 3116-76-5 | 双氯西林 | ≥95 | % |
| 7177-50-6 | 萘夫西林钠一水合物 | ≥89 | % |
| 61477-96-1 | 哌拉西林 | ≥95 | % |
| 37091-66-0 | 苯咪青霉素 | ≥95 | % |
| 132-92-3 | 甲氧西林钠 | ≥95 | % |
详细介绍
11种青霉素类抗生素固体混标/GB 31656.12-2021
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.
| CERTIFIED | |||||
| Component No. |
Purity (%) (纯度) |
Weight (ug) |
Uncertainty (%) |
||
| 1 | Amoxicillin | 26787-78-0 | 99.7 | 100.2 | 1.0 |
| 2 | Ampicillin | 69-53-4 | 98.0 | 101.6 | 1.0 |
| 3 | Benzylpenicillin Potassium | 113-98-4 | 97.7 | 114.0 | 1.0 |
| 4 | Penicillin V | 87-08-1 | 98.0 | 101.6 | 1.0 |
| 5 | Oxacillin Sodium Salt | 1173-88-2 | 95.6 | 111.0 | 1.0 |
| 6 | Cloxacillin Sodium Salt Monohydrate | 7081-44-9 | 99.0 | 110.2 | 1.0 |
| 7 | Dicloxacillin | 3116-76-5 | 97.5 | 102.2 | 1.0 |
| 8 | Nafcillin Sodium Monohydrate | 7177-50-6 | 96.6 | 114.2 | 1.0 |
| 9 | Piperacillin | 61477-96-1 | 98.0 | 102.0 | 1.0 |
| 10 | Azlocillin | 37091-66-0 | 96.7 | 103.8 | 1.0 |
| 11 | Methicillin Sodium Salt | 132-92-3 | 98.5 | 107.2 | 1.0 |
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.
| CERTIFICATE ON | QC SIGNATURE | |
| - |
|
RM Release |
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