Compare products Close window [X]

 
 
  Remove Remove Remove Remove Remove Remove Remove
Sorafenib EP Impurity E
Dasatinib Dichloro Impurity
Nintedanib Impurity 52
Clobetasol Impurity 1
Trimethoprim Impurity 1
Sacubitril Impurity 33
Clobetasol Propionate Related Compound 1
Title Sorafenib EP Impurity E Dasatinib Dichloro Impurity Nintedanib Impurity 52 Clobetasol Impurity 1 Trimethoprim Impurity 1 Sacubitril Impurity 33 Clobetasol Propionate Related Compound 1
Add to cart
Description

Sorafenib EP Impurity E is chemically 4,4′-[Carbonylbis(azanediyl-4,1-phenyleneoxy)]bis(N-methylpyridine-2-carboxamide) (as per EP)
N,N’-Bis{4-[2-(N-methylcarbamoyl)-4-pyridyloxy]phenyl}urea (as per USP).
It is also known as Sorafenib USP Impurity E.
Sorafenib EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Sorafenib EP Impurity E 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 Sorafenib.

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.

Dasatinib Dichloro Impurity is chemically N-(2-Chloro-6-methylphenyl)-2-[(6-chloro-2-methyl-4-pyrimidinyl)amino]-5-thiazolecarboxamide ;.
It is also known as Dasatinib Dichloro Impurity ; .
Dasatinib Dichloro Impurity is supplied with detailed characterization data compliant with regulatory guideline. Dasatinib Dichloro Impurity 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 Dasatinib.

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.

Nintedanib Impurity 52 is chemically Methyl 2-oxoindoline-6-carboxylate. Nintedanib Impurity 52 is supplied with detailed characterization data compliant with regulatory guideline. Nintedanib Impurity 52 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 Nintedanib.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.

Clobetasol Impurity 1 is chemically 9-Fluoro-11-beta-21-Dihydroxy-16-Methylpregna-1, 4, 16-triene-3, 20-Dione.
Clobetasol Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Clobetasol Impurity 1 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 Clobetasol Propionate.

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.

Trimethoprim Impurity 1 is chemically 5-(3,4,5-trimethoxybenzyl)pyrimidine-2,4(1H,3H)-dione. Trimethoprim Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Trimethoprim Impurity 1 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 Trimethoprim.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.

Sacubitril Impurity 33 is chemically (R)-3-([1,1′-Biphenyl]-4-yl)-2-((tert-butoxycarbonyl)amino)propyl acetate.
Sacubitril Impurity 33 is supplied with detailed characterization data compliant with regulatory guideline. Sacubitril Impurity 33 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 Sacubitril.

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.

Clobetasol Propionate Related Compound 1 is chemically (4aS,4bS,5aS,6aS,7S,8R,9aS,11S)-11-fluoro-7-(2-hydroxyacetyl)-4a,6a,8-trimethyl-5a,6,6a,7,8,9,9a,9b,10,11-decahydrocyclopenta[1,2]phenanthro[4,4a-b]oxiren-2(4aH)-one.
Clobetasol Propionate Related Compound 1 is supplied with detailed characterization data compliant with regulatory guideline. Clobetasol Propionate Related Compound 1 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 Clobetasol Propionate.

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.

Availability In stock In stock In stock In stock In stock In stock In stock
CAS No 284670-98-0 302964-08-5 14192-26-8 59860-99-0 93885-69-9 219718-02-2 61618-89-1
Inv. Status In Stock In Stock In Stock In Stock Custom Synthesis In Stock In Stock
Mol.F. C27H24N6O5 C16H13ClN5OS C10H9NO3 C22H27FO4 C14H16N2O5 C22H27NO4 C22H27FO4
ISP CAT No ISP-S012017   ISP-N023072   ISP-T033014 ISP-S020041  
Mol.Wt. 512.5 394.3 191.2 374.5 292.3 369.5 374.5