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Merck

PHR1709

Supelco

维生素C杂质D

Pharmaceutical Secondary Standard; Certified Reference Material

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别名:
Methyl-D-Sorbosonate (Ascorbic Acid Imp D), Methyl-D-Sorbosonate
分類程式碼代碼:
41116107
NACRES:
NA.24

等級

certified reference material
pharmaceutical secondary standard

品質等級

agency

traceable to Ph. Eur. Y0001170

API 家族

ascorbic acid

CofA

current certificate can be downloaded

包裝

ampule of 30 mg

應用

pharmaceutical (small molecule)

格式

neat

儲存溫度

2-8°C

一般說明

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Ascorbic acid Impurity D is an impurity of ascorbic acid (AA), which is also known as vitamin C. It is found in plant tissues and exhibits antioxidant property.

應用

Ascorbic acid may be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical formulations using automatic potentiometric flow titration method.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

分析報告

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

其他說明

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

腳註

To see an example of a Certificate of Analysis for this material enter LRAA7297 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Automatic potentiometric flow titration procedure for ascorbic acid determination in pharmaceutical formulations
Paim SPA, et al.
Journal of Pharmaceutical and Biomedical Analysis, 28(6), 1221-1225 (2002)

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