19 Resultat för: "VARLP090222USPH00045"
tert-Octylamine, 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'-De(dimethylamino)-3'-oxoazithromycin, 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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Dimethylethylamine 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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Why Choose Corning Fetal Bovine Serum?
Our vertically integrated FBS serum supply chain, from collection to scientist, allows us to provide a consistent supply of FBS.
Amoxicilloic Acid Dimers 1 and 2, 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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Tetramethyl Ethylene Diamine, 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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Pyrrolic acid Derivative, 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'-(N,N-Didemethyl)azithromycin;, 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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Ethylpyrazinediethanol, 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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Pyrazinediethanol, 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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2,3-Dimethyl-2,3-butanediamine Dihydrochloride, 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'-(N,N-Didemethyl)-3'-N-formylazithromycin, 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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Desfluorociprofloxacin 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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Decarboxy Levofloxacin, 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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TEMED Dihydrochloride, 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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Floxacin Amine, 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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Bis(dimethylaminoethyl) Ether Dihydrochloride, 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'-Demethyl-3'-N-[(4-methylphenyl)sulfonyl]azithromycin, 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.