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Avibactam Impurity 19
Testosterone Impurity 24
1,3 -Butane Sultone
(S)-Desmethyl Rabeprazole Sodium Salt
R-Thiotic Acid Tromethamine
Rucaparib Ring-Opening Impurity
Moxifloxacin Formyl
Rac Albuterol D9
Cladribine EP Impurity E
Title Avibactam Impurity 19 Testosterone Impurity 24 1,3 -Butane Sultone (S)-Desmethyl Rabeprazole Sodium Salt R-Thiotic Acid Tromethamine Rucaparib Ring-Opening Impurity Moxifloxacin Formyl Rac Albuterol D9 Cladribine EP Impurity E
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Description

Avibactam Impurity 19 is chemically Ethyl (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate.
Avibactam Impurity 19 is supplied with detailed characterization data compliant with regulatory guideline. Avibactam Impurity 19 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 Avibactam.

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.

Testosterone Impurity 24 is chemically (8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl oleate. Testosterone Impurity 24 is supplied with detailed characterization data compliant with regulatory guideline. Testosterone Impurity 24 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 Testosterone.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.

1,3 -Butane Sultone is chemically 5-Methyl-1,2-oxathiolane 2,2-dioxide.
1,3 -Butane Sultone is supplied with detailed characterization data compliant with regulatory guideline. 1,3 -Butane Sultone 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 Miscellaneous.

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.

(S)-Desmethyl Rabeprazole Sodium Salt is chemically Sodium (S)-2-(((4-(3-methoxypropoxy)pyridin-2-yl)methyl)sulfinyl)benzo[d]imidazol-1-ide.
(S)-Desmethyl Rabeprazole Sodium Salt is supplied with detailed characterization data compliant with regulatory guideline. (S)-Desmethyl Rabeprazole Sodium Salt 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 Rabeprazole.

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.

R-Thiotic Acid Tromethamine is chemically 2-Amino-2-(hydroxymethyl)propane-1,3-diol (R)-5-(1,2-dithiolan-3-yl)pentanoate. R-Thiotic Acid Tromethamine is supplied with detailed characterization data compliant with regulatory guideline. R-Thiotic Acid Tromethamine 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 Thioctic 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.

Rucaparib Ring-Opening Impurity is chemically 3-(2-aminoethyl)-6-fluoro-2-(4-((methylamino)methyl)phenyl)-1H-indole-4-carboxylic acid.
Rucaparib Ring-Opening Impurity is supplied with detailed characterization data compliant with regulatory guideline. Rucaparib Ring-Opening 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 Rucaparib.

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.

Moxifloxacin Formyl is chemically 1-cyclopropyl-6-fluoro-7-((4aS,7aS)-1-formyloctahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.
Moxifloxacin Formyl is supplied with detailed characterization data compliant with regulatory guideline. Moxifloxacin Formyl 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 Moxifloxacin.

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.

Rac Albuterol D9 is chemically 4-(1-Hydroxy-2-((2-(methyl-d3)propan-2-yl-1,1,1,3,3,3-d6)amino)ethyl)-2-(hydroxymethyl)phenol.
Rac Albuterol D9 is supplied with detailed characterization data compliant with regulatory guideline. Rac Albuterol D9 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 Salbutamol .

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.

Cladribine EP Impurity E is chemically 2-Deoxy-d-erythro-pentofuranose (2-deoxy-d-ribose),.
Cladribine EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Cladribine 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 Cladribine.

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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CAS No 1416134-47-8 97814-32-9 3289-23-4   137314-40-0     1173021-73-2 1831121-84-6
Inv. Status Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis Custom Synthesis In Stock Custom Synthesis In Stock
Mol.F. C15H22N2O3 C37H60O3 C4H8O3S C17H18N3O3S : Na C8H14O2S2 : C4H11NO3 C19H20FN3O2 C22H24FN3O5 C13H12D9NO3 C5H10O4
ISP CAT No ISP-A130024 ISP-T021096 ISP-M039336 ISP-R006026 ISP-T054011 ISP-R055017 ISP-M033026 ISP-S003D02  
Mol.Wt. 278.4 552.9 136.2 344.42 : 23.0 206.3 : 121.1 341.4 429.4 248.4 134.1