组分信息
| CAS号 | 名称 | 标准值 | 单位 |
|---|---|---|---|
| 1115-70-4 | 盐酸二甲双胍 | 100 | μg/mL |
| 1190-53-0 | 盐酸丁双胍 | 100 | μg/mL |
| 834-28-6 | 盐酸苯乙福明 | 100 | μg/mL |
| 122320-73-4 | 罗格列酮 | 100 | μg/mL |
| 112529-15-4 | 盐酸吡格列酮 | 100 | μg/mL |
| 135062-02-1 | 瑞格列奈 | 100 | μg/mL |
| 29094-61-9 | 格列吡嗪 | 100 | μg/mL |
| 64-77-7 | 甲苯磺丁脲 | 100 | μg/mL |
| 21187-98-4 | 格列齐特 | 100 | μg/mL |
| 26944-48-9 | 格列波脲 | 100 | μg/mL |
| 10238-21-8 | 格列本脲 | 100 | μg/mL |
| 93479-97-1 | 格列美脲 | 100 | μg/mL |
| 33342-05-1 | 格列喹酮 | 100 | μg/mL |
详细介绍
13种降糖药物混标/2022国抽保健品/2009-029/2011-008/2013-001/2023国抽保健品/保质期6个月
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.
冷冻(-18±5)℃,置于阴凉处
| CERTIFIED | |||||
|
Component No. (组分数) |
Concentration (μg/mL) (浓度) |
Relative Expanded Uncertainty(%) (k=2) (相对扩展不确定度) |
|||
| 1 | 1 | Metformin Hydrochloride1 (盐酸二甲双胍) | 1115-70-4 | 100(free base) | 3 |
| 2 | 2 | Buformin Hydrochloride1 (盐酸丁双胍) | 1190-53-0 | 100(free base) | 3 |
| 3 | 3 | Phenformin Hydrochloride1 (盐酸苯乙福明) | 834-28-6 | 100(free base) | 3 |
| 4 | 4 | Rosiglitazone Maleate2 ( 马来酸罗格列酮) | 155141-29-0 | 100(free base) | 3 |
| 5 | 5 | Pioglitazone Hydrochloride1 (盐酸吡格列酮) | 112529-15-4 | 100(free base) | 3 |
| 6 | 6 | Repaglinide (瑞格列奈) | 135062-02-1 | 100 | 3 |
| 7 | 7 | Glipizide (格列吡嗪) | 29094-61-9 | 100 | 3 |
| 8 | 8 | Tolbutamide (甲苯磺丁脲) | 64-77-7 | 100 | 3 |
| 9 | 9 | Gliclazide (格列齐特) | 21187-98-4 | 100 | 3 |
| 10 | 10 | Glibornuride (格列波脲) | 26944-48-9 | 100 | 3 |
| 11 | 11 | Glibenclamide (格列本脲) | 10238-21-8 | 100 | 3 |
| 12 | 12 | Glimepiride (格列美脲) | 93479-97-1 | 100 | 3 |
| 13 | 13 | Gliquidone (格列喹酮) | 33342-05-1 | 100 | 3 |
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 | |
| 2023-Feb-27 |
|
RM Release |
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