12种降压药物混标/保健品中非法添加剂/2022国抽保健品/BJS 201710/2009032&2014008方法/2023国抽保健品/保质期2个月,标准溶液,溶剂:乙腈, 100μg/mL

产品编号:西域质检-TM13600

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
西域质检-TM13600
2595.00 杭州 北京(现货)

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组分信息

CAS号 名称 标准值 单位
29122-68-7 阿替洛尔 100 μg/mL
4205-91-8 盐酸可乐定 100 μg/mL
63675-72-9 尼索地平 100 μg/mL
62571-86-2 卡托普利 100 μg/mL
19237-84-4 盐酸哌唑嗪 100 μg/mL
50-55-5 利血平 100 μg/mL
21829-25-4 硝苯地平 100 μg/mL
111470-99-6 苯磺酸氨氯地平 100 μg/mL
39562-70-4 尼群地平 100 μg/mL
66085-59-4 尼莫地平 100 μg/mL
72509-76-3 非洛地平 100 μg/mL
58-93-5 氢氯噻嗪 100 μg/mL

详细介绍

12种降压药物混标/保健品中非法添加剂/2022国抽保健品/BJS 201710/2009032&2014008方法/2023国抽保健品/保质期2个月

Reference Material

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.

Product Name(产品名称) 12 Hypotensive Drug Mix in Acetonitrile,100μg/mL(乙腈中12种降压药物混标)
Part Number(产品编号) 81112GH
Lot Number(产品批号) 23020701
Expiry Date(失效日期) 2023-Apr-21____________________________________________________
Storage(存储条件)   (-18±5)℃,Keep in the shade
  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
2
3
4
5
6
7
8
9
10
11
12
,
Note

1.The above components are calculated in the form of free states.(上述组分以游离态的形式计算)
2.The standard value of amlodipine besilate  is  amlodipine.(苯磺酸氨氯地平的标准值为氨氯地平)

Intended Use

This RM is intended for use in a laboratory as a calibration and quality control standard or in method development for analytical techniques.

Uncertainty

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.

Traceability

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.

Homogeneity

Random replicate samples of the final packaged RM have been analysed to prove homogeneity consistent with ISO 17034.

Storage

The RM should be stored in the original sealed bottle at the indicated temperature.

CERTIFICATE    ON QC    SIGNATURE
2023-Feb-22 RM Release

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