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N-Nitroso Oxymetazoline
Armodafinil Impurity 1
N-Nitroso-Betahistine
Xylometazoline EP Impurity D
Orphenadrine USP Related Compound C (HCl salt)
Etoricoxib Impurity 18
Atropine Sulfate Monohydrate
Zolmitriptan Nitroso Impurity 6
Xanthine
Title N-Nitroso Oxymetazoline Armodafinil Impurity 1 N-Nitroso-Betahistine Xylometazoline EP Impurity D Orphenadrine USP Related Compound C (HCl salt) Etoricoxib Impurity 18 Atropine Sulfate Monohydrate Zolmitriptan Nitroso Impurity 6 Xanthine
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Description

N-Nitroso Oxymetazolineis chemically 6-(tert-butyl)-2,4-dimethyl-3-((1-nitroso-4,5-dihydro-1H-imidazol-2-yl)methyl)phenol. N-Nitroso Oxymetazoline is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Oxymetazoline 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 Oxymetazoline.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.

Armodafinil Impurity 1 is chemically (R)-2-(Benzhydrylsulfinyl)acetic acid.
Armodafinil Impurity 1 is supplied with detailed characterization data compliant with regulatory guideline. Armodafinil 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 Armodafinil.

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-Nitroso-Betahistine is chemically N-Methyl-N-(2-(pyridin-2-yl)ethyl)nitrous amide.
N-Nitroso-Betahistine is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso-Betahistine 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 Betahistine.

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.

Xylometazoline EP Impurity D is chemically 1-(1,1-dimethylethyl)-3,5-dimethylbenzene (as per EP).
Xylometazoline EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Xylometazoline EP 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 Xylometazoline.

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.

Orphenadrine USP Related Compound C (HCl salt) is chemically (N-Methyl-2-[phenyl(o-tolyl)methoxy]ethanamine hydrochloride) (as per USP).
It is also known as Demethyl orphenadrine hydrochloride ; Tofenacin hydrochloride.
Orphenadrine USP Related Compound C (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Orphenadrine USP Related Compound C (HCl 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 Orphenadrine.

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.

Etoricoxib Impurity 18 is chemically 2-methyl-5-(2-(4-(methylsulfonyl)phenyl)acetyl)pyridine 1-oxide.
Etoricoxib Impurity 18 is supplied with detailed characterization data compliant with regulatory guideline. Etoricoxib Impurity 18 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 Etoricoxib.

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.

Atropine Sulfate Monohydrate is chemically Bis[(1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]oct-3-yl (2RS)-3-hydroxy-2-phenylpropanoate] sulfate monohydrate..
Atropine Sulfate Monohydrate is supplied with detailed characterization data compliant with regulatory guideline. Atropine Sulfate Monohydrate 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 Atropine.

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.

Zolmitriptan Nitroso Impurity 6 is chemically (S)-N-(2-(5-(2-Amino-3-hydroxypropyl)-1H-indol-3-yl)ethyl)-N-methylnitrous amide.
Zolmitriptan Nitroso Impurity 6 is supplied with detailed characterization data compliant with regulatory guideline. Zolmitriptan Nitroso Impurity 6 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 Zolmitriptan.

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.

Xanthine is chemically 3,7-Dihydro-1H-purine-2,6-dione.
Xanthine is supplied with detailed characterization data compliant with regulatory guideline. Xanthine 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 Xanthine.

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   112111-45-2 32635-81-7 98-19-1 10488-36-5 1027162-35-1 5908-99-6   69-89-6
Inv. Status Custom Synthesis Custom Synthesis In Stock In Stock In Stock Custom Synthesis In Stock Custom Synthesis Custom Synthesis
Mol.F. C16H23N3O2 C15H14O3S C8H11N3O C12H18 C17H21NO : HCl C15H15NO4S C17H23NO3 : 1/2(H2SO4) : 1/2(H2O) C14H20N4O2 C5H4N4O2
ISP CAT No ISP-O030007 ISP-A127003 ISP-B007008 ISP-X001005 ISP-O015020 ISP-E030023 ISP-A029000 ISP-Z004047 ISP-X005001
Mol.Wt. 289.4 274.3 165.2 162.3 255.4 : 36.5 305.4 289.4 : 1/2(98.1) : 1/2(18.0) 276.3 152.1