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![5H-二苯并[b,f]氮杂 Pharmaceutical Secondary Standard; Certified Reference Material](/deepweb/assets/sigmaaldrich/product/structures/396/216/18f00414-a76e-46d7-90cf-820ad902e559/640/18f00414-a76e-46d7-90cf-820ad902e559.png)
等级
certified reference material
pharmaceutical secondary standard
质量水平
Agency
traceable to USP 1337004
API类
iminodibenzyl
CofA
current certificate can be downloaded
包装
pkg of 100 mg
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
pharmaceutical (small molecule)
包装形式
neat
储存温度
2-30°C
SMILES字符串
C1Cc2ccccc2Nc3ccccc13
InChI
1S/C14H13N/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)15-13/h1-8,15H,9-10H2
InChI key
ZSMRRZONCYIFNB-UHFFFAOYSA-N
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一般描述
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
应用
Iminodibenzyl may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by thin layer chromatography and spectrophotometry techniques.
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.
分析说明
These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.
其他说明
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.
附注
To see an example of a Certificate of Analysis for this material enter LRAA8622 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.
警示用语：
Warning
危险声明
危险分类
Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Impurities in drugs I: Imipramine, desipramine, and their formulations.
McErlane KM, et al.
Journal of Pharmaceutical Sciences, 66(7), 1015-1018 (1977)
B A el-Zeany et al.
Journal of pharmaceutical and biomedical analysis, 33(4), 775-782 (2003-11-19)
Two spectrophotometric methods for the determination of imipramine in presence of iminodibenzyl as an impurity are described. The first method is a ratio-spectra first derivative spectrophotometry, the signals were measured at 240.2 nm for imipramine. Calibration graph was found linear
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