Compare products Close window [X]

Lurasidone Impurity Kis chemically (2-((1,3-dioxooctahydro-2H-4,7-methanoisoindol-2-yl)methyl)cyclohexyl)methyl 4-(benzo[d]isothiazol-3-yl)piperazine-1-carboxylate. Lurasidone Impurity K is supplied with detailed characterization data compliant with regulatory guideline. Lurasidone Impurity K 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 Lurasidone.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.

Paroxetine Impurity 4 is chemically 3-(Benzo[d][1,3]dioxol-5-yloxy)-4-(4-fluorophenyl)-1-methylpiperidine.
Paroxetine Impurity 4 is supplied with detailed characterization data compliant with regulatory guideline. Paroxetine Impurity 4 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 Paroxetine.

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.

Azilsartan Impurity D is chemically (Z)-3-((2′-(N’-Hydroxycarbamimidoyl)-[1,1′-biphenyl]-4-yl)methyl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazole-4-carboxylic acid.
Azilsartan Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Azilsartan Impurity D 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 Azilsartan.

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 EP Impurity K is chemically 9-Fluoro-11β,17-dihydroxy-16β-methyl-3,20-dioxopregna-1,4-dien-21-yl propanoate (as per EP).
It is also known as Betamethasone 21-propionate.
Clobetasol Propionate EP Impurity K is supplied with detailed characterization data compliant with regulatory guideline. Clobetasol Propionate EP Impurity K 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.

Meclizine N-Oxide (N4-oxide) is chemically 4-((4-Chlorophenyl)(phenyl)methyl)-1-(3-methylbenzyl)piperazine 1-oxide.
Meclizine N-Oxide (N4-oxide) is supplied with detailed characterization data compliant with regulatory guideline. Meclizine N-Oxide (N4-oxide) 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 Meclizine.

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.

Umeclidinium Bromide Impurity 9 is chemically Phenyl(quinuclidin-4-yl)methanone.
Umeclidinium Bromide Impurity 9 is supplied with detailed characterization data compliant with regulatory guideline. Umeclidinium Bromide Impurity 9 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 Umeclidinium Bromide.

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.

Metacresol EP Impurity K is chemically 4-Ethylphenol (As per EP).
It is also known as p-ethylphenol (EP).
Metacresol EP Impurity K is supplied with detailed characterization data compliant with regulatory guideline. Metacresol EP Impurity K 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 Metacresol.

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.

Meropenem Trihydrate is chemically (4R,5S,6S)-3-(((3S,5S)-5-(Dimethylcarbamoyl)pyrrolidin-3-yl)thio)-6-((R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid trihydrate.
Meropenem Trihydrate is supplied with detailed characterization data compliant with regulatory guideline. Meropenem Trihydrate 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 Meropenem.

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.

Dehydrosilybin is chemically 3,5,7-Trihydroxy-2-((2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-4H-chromen-4-one.
Dehydrosilybin is supplied with detailed characterization data compliant with regulatory guideline. Dehydrosilybin 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 Silibinin.

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.

N-Acetyl Memantine is chemically N-(3,5-Dimethyltricyclo[3.3.1.13,7]dec-1-yl)acetamide.
N-Acetyl Memantine is supplied with detailed characterization data compliant with regulatory guideline. N-Acetyl Memantine 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 Memantine.

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.

Amidotrizoic Acid EP Impurity E is chemically 3-(Acetylamino)-5-(diacetylamino)-2,4,6-triiodobenzoic acid (as per EP).
Amidotrizoic Acid EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Amidotrizoic Acid 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 Amidotrizoic Acid.

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.

Larotrectinib Impurity 12 is chemically (R)-5-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine.
Larotrectinib Impurity 12 is supplied with detailed characterization data compliant with regulatory guideline. Larotrectinib Impurity 12 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 Larotrectinib.

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.

Nitrofural EP Impurity B is chemically (5-Nitrofuran-2-yl)methylene diacetate (as per EP). Nitrofural EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Nitrofural EP Impurity B 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 Nitrofural.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.

pCl-L-Phe Cetrorelix is chemically (S)-1-(((R)-2-((S)-2-((S)-2-((R)-2-((S)-2-((R)-2-acetamido-3-(naphthalen-2-yl)propanamido)-3-(4-chlorophenyl)propanamido)-3-(pyridin-3-yl)propanamido)-3-hydroxypropanamido)-3-(4-hydroxyphenyl)propanamido)-5-ureidopentanoyl)-L-leucyl-L-arginyl)-N-((R)-1-amino-1-oxopropan-2-yl)pyrrolidine-2-carboxamide 2,2,2-trifluoroacetate.
pCl-L-Phe Cetrorelix is supplied with detailed characterization data compliant with regulatory guideline. pCl-L-Phe Cetrorelix 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 Cetrorelix.

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.