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他达那非(EC 17025)_171596-29-5
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他达那非(EC 17025)

BW905008 {{goodObj.price > 0 ? '¥' + goodObj.price : '咨询'}} ¥{{goodObj.sell_price || 0}} 咨询 171596-29-5 10mg {{goodObj.date}} 秦境标物 {{item.norm}} 99.9% {{inventory}}
他达那非介绍:

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 ISO9001.

Product Name

Tadalafil

Product Code

BW905008


Lot Number

23061531

CAS No.

171596-29-5

Mol. Formula

C22H19N3O4

Mol. Weight

389.40

Certified on

2 Jun 2023

Expiry Date

1 Jun 2025

Storage Temp

20°C ± 4°C

Specification

10 mg

CERTIFIED

Purity

CERTIFIED

Expanded Uncertainty (U)

Approved by

99.9%

0.5%


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 characterisation, homogeneity and stability testing. Stability values are based on real evidence opposed to simulation.

The producer certifies that this reference material meets the specification stated in this certificate until the expiry date, provided it is stored unopened at the recommended temperature herein. Product warranties for this reference material are set out in the terms and conditions of purchase.

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.

Safety

Proper precautions should be observed while handling. See Safety Data Sheet.

Traceability

The balances used for gravimetric measurements are calibrated with weights traceable to the national standards (DKD). The calibration of the balances is verified daily internally and annually by an external7 accredited calibration service. Chromatographic methods are traceable to the International System of Units (SI).

Homogeneity

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

Storage

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

Instructions for use

It is recommended to use 1 mg as the minimum sample size and if less material is used, to increase the certified uncertainty by a factor of two for half sample and four for a quarter of sample. If storage after opening is necessary, the RM should be tightly closed and kept from light and moisture. If the RM was in a sealed ampoule, it should be transferred to a vial with minimum head space.


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一、标准名称及标准号
标准名称 保健食品中非法添加化学药物检测方法——他达那非的测定
标准号 国家食品药品监督管理局药品检验补充检验方法和检验项目批准件(2009020)
二、适用范围
适用范围 适用于保健食品(如声称缓解体力疲劳、改善性功能等类产品)中非法添加他达那非(CAS:171596-29-5)的定性及定量检测。
三、核心检测方法
方法原理 高效液相色谱-串联质谱法(HPLC-MS/MS),通过保留时间和特征离子对进行定性,外标法定量。
色谱条件 色谱柱:C18反相色谱柱;流动相:乙腈-0.1%甲酸水溶液梯度洗脱;流速:0.3 mL/min。
四、检出限与定量限
检出限(LOD) 0.05 mg/kg
定量限(LOQ) 0.1 mg/kg
五、质控样品要求
空白对照 需使用不含目标物质的同类基质样品作为空白对照。
加标回收率 添加浓度应覆盖定量限至两倍实际样品浓度,回收率需在80%-120%之间。
六、关键实验步骤
样品前处理 样品经粉碎后,用甲醇-水(70:30)溶液超声提取,离心过滤后进样分析。
质谱条件 电离模式:电喷雾离子源(ESI+);监测离子对:m/z 390.2→268.1(定量离子),390.2→136.1(定性离子)。
七、特别说明
干扰排除 需验证基质中是否含类似结构的衍生物(如西地那非)以避免假阳性结果。
方法确认 实验室首次使用本方法时需进行方法学验证,包括线性、精密度、稳定性等指标。

以上信息仅供参考,请以相应标准的原文为准!