PHR2310
Loratadine Impurity A
certified reference material, pharmaceutical secondary standard
别名:
Ethyl 4-(13-chloro-2-hydroxy-4-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-yl)piperidine-1-carboxylate
产品名称
Loratadine Impurity A, certified reference material, pharmaceutical secondary standard
SMILES string
Clc1cc2c(cc1)C(c4ncccc4CC2)(O)C3CCN(CC3)C(=O)OCC
InChI
1S/C22H25ClN2O3/c1-2-28-21(26)25-12-9-17(10-13-25)22(27)19-8-7-18(23)14-16(19)6-5-15-4-3-11-24-20(15)22/h3-4,7-8,11,14,17,27H,2,5-6,9-10,12-13H2,1H3
InChI key
WVWGYTXDYNKXEY-UHFFFAOYSA-N
grade
certified reference material
pharmaceutical secondary standard
API family
loratadine
form
solid
packaging
pkg of 50 mg
pkg of
application(s)
pharmaceutical
storage temp.
-10 to -25°C
Quality Level
Analysis Note
These secondary standards offer multi-traceability to the USP and EP primary standards, where they are available.
Application
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.
General description
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
Other Notes
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
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