6083 Results for: "Analytical Standards"
Fluticasone Propionate Acid, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Diphthalimido Morpholinone Analog, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Bis(2-methylaminoethyl) Ether, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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N-Ethyl Quetiapine, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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N6-(1-Iminoethyl)-D-lysine, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Budesonide 9(11)-ene, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Levetiracetam Hydroxybutyramide Analog, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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ICP-MS analytes B for 6020 CLP-M, Specpure®
Supplier: Thermo Fisher Scientific
11 elements
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Desethylamiodarone, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Desiodoamiodarone, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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4-Methylacetophenone, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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3-Hydroxy Desloratadine, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Olanzapine, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Fluticasone, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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6-Methyl-4-phenylchromanone, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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N-Hydroxy Desloratadine, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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VWR® PESTINORM®, 2-Propanol, Secondary Reference Standard for GC
Supplier: VWR Chemicals
A secondary GC solvent reference standard for various chromatographic and analytical applications.
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VWR® PESTINORM®, Methanol, Secondary Reference Standard for GC
Supplier: VWR Chemicals
A secondary GC solvent reference standard for various chromatographic and analytical applications.
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VWR® PESTINORM®, Ethyl Acetate, Secondary Reference Standard for GC
Supplier: VWR Chemicals
A secondary GC solvent reference standard for various chromatographic and analytical applications.
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Atorvastatin Epoxy Tetrahydrofuran Analog, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Bis(2-methylaminoethyl) Ether Hydrochloride, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Rivaroxaban N-acyl glycolic acid, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Methyl myristate 99% analytical standard for GC
Supplier: Thermo Fisher Scientific
Methyl myristate 99% analytical standard for GC
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VWR® PESTINORM®, Tetrahydrofuran (THF), Secondary Reference Standard for GC
Supplier: VWR Chemicals
A secondary GC solvent reference standard for various chromatographic and analytical applications.
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VWR® PESTINORM®, Acetone, Secondary Reference Standard for GC
Supplier: VWR Chemicals
A secondary GC solvent reference standard for various chromatographic and analytical applications.
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Potassium permanganate 0.02M (0.1N), meets analytical specification of Ph.Eur. standard volumetric solution
Supplier: Thermo Fisher Scientific
Potassium permanganate 0.02M (0.1N), meets analytical specification of Ph.Eur. standard volumetric solution
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VWR®, Cold Cranking Simulator (CCS) viscosity standards
Supplier: VWR Chemicals
High quality CCS viscosity standards are ideal for the calibration and verification of analytical equipment used in Cold Cranking Simulator (CCS) testing.
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Donepezil Quaternary Salt, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Budesonide Acetaldehyde Acetal, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.
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Tolyloyl Propionic Acid, Pharmaceutical Analytical Impurities
Supplier: USP
Pharmaceutical Analytical Impurities are released through a USP quality process designed to ensure identity and quality appropriate for analytical applications. These impurities are supported with a product information sheet for each batch.