グレード
certified reference material
pharmaceutical secondary standard
品質水準
APIファミリー
magnesium stearate
包装
ampule of 2.5 g
アプリケーション
pharmaceutical (small molecule)
フォーマット
neat
保管温度
2-30°C
詳細
Magnesium stearate is commonly utilized as a lubricant in pharmaceutical formulations to avoid the excipient blend from the formulation contents from sticking to the manufacturing equipment.
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.
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.
アプリケーション
Magnesium stearate may be used as an excipient for the manufacturing of atorvastatin drug and poloxamers. The determination of the analyte in pharmaceutical formulations can be carried out by chromatography and colorimetric methods.
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.
アナリシスノート
このような2次標準は、USP、EP(PhEur)、BPの1次標準にマルチトレーサビリティを提供します。
その他情報
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.
脚注
To see an example of a Certificate of Analysis for this material enter LRAA1467 in the slot below. This is an example certificate only and may not be the lot that you receive.
保管分類コード
11 - Combustible Solids
WGK
nwg
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
労働安全衛生法名称等を表示すべき危険物及び有害物
名称等を表示すべき危険物及び有害物
労働安全衛生法名称等を通知すべき危険物及び有害物
名称等を通知すべき危険物及び有害物
Choose from one of the most recent versions:
試験成績書(COA)
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Analysis of magnesium from magnesium stearate in pharmaceutical tablet formulations using hydrophilic interaction liquid chromatography with nano quantity analyte detection
Journal of Pharmaceutical and Biomedical Analysis, 78, 112-117 (2013)
Liquid chromatographic determination of atorvastatin in bulk drug, tablets, and human plasma
Journal of Liquid Chromatography and Related Technologies, 27(1), 83-93 (2004)
Quantitation of poloxamers in pharmaceutical formulations using size exclusion chromatography and colorimetric methods
Journal of Pharmaceutical and Biomedical Analysis, 35(5), 1127-1142 (2004)
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