-100%
Timolol EP Impurity A
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- Product Overview
- Description
- Technical Data
Description
Chemical Name: (2R)-1-[(1,1-Dimethylethyl)amino]-3-[[4-(morpholin-4-yl)-1,2,5-thiadiazol-3-yl]oxy]propan-2-ol (as per EP) ; (R)-1-(tert-Butylamino)-3-(4-morpholino-1,2,5-thiadiazol-3-yloxy)propan-2-ol (as per USP)Synonym: (R)-Timolol (EP) ; Timolol USP Related Compound A Shipping Temperature: Ambient HSN Code: 38229010Country of Origin: IndiaSmiles: CC(C)(C)NC[C@@]([H])(O)COC1=NSN=C1N2CCOCC2
Additional Information
Timolol EP Impurity A is chemically (2R)-1-[(1,1-Dimethylethyl)amino]-3-[[4-(morpholin-4-yl)-1,2,5-thiadiazol-3-yl]oxy]propan-2-ol (as per EP) ; (R)-1-(tert-Butylamino)-3-(4-morpholino-1,2,5-thiadiazol-3-yloxy)propan-2-ol (as per USP). It is also known as (R)-Timolol (EP) ; Timolol USP Related Compound A. Timolol EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Timolol EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Timolol.The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.
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