181377 Results for: "Batch Pressure Filter Cloth"
Celecoxib, 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 p-Toluate, 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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Aminophenylmorpholinone, 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 Glycolic Acid 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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N-Methyl Lacosamide, 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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Desfluorocitalopram Oxalate, 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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Tetrahydrothienopyridine 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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Dehydro 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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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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Clopidogrel Amide, 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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Azacitidine Isomer -3, 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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(R)-Clopidogrel Carboxylic 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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Tolyloyl Propionamide, 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 Open Ring, 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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MF Endo broth
Supplier: Cytiva (Formerly Pall Lab)
M-Endo broth is used for the estimation of coliform bacteria in water samples using the membrane filtration technique. It is possible to remove bacteria from fluids by passing them through filters with such small pore size that bacteria are arrested. This filtration technique enables fairly large volumes of water to pass rapidly under pressure, but prevents the passage of any bacteria present. These nutrients are retained on the surface of the membrane which is then brought into contact with suitable liquid nutrients. These diffuse upwards through the pores thereby inducing the organisms to grow as surface colonies which can be counted.
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Volumetric flasks, class A, white markings, USP batch certificate, BLAUBRAND®
Supplier: Brand
Borosilicate glass 3.3, amber, with amber glass stopper or PP stopper.
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Recirculating air filter system and extraction units
Supplier: asecos
Recirculating air filter system UFA.20.30
Avoid complex wall, ceiling and roof penetrations and costly extract systems. Safe capturing of escaping vapours at the point where they are released or produced.
High flexibility in choosing the installation location
Active personal protection through safe capture of harmful vapours with retention in the filter system
Very low noise, ~39 dB(A)
ATEX complient: CE II 3/-G Ex ic nA IIB T4 Gc
Housing made of sheet-steel plastic laminated
With multistage filter system and power cord
Incl. VDE tested extraction and filter monitoring
Optical and acoustical alarm including potential-free alarm contact
Dimensions W×D×H: 305×555×210 mm
The plug-in recirculating air filter system UFA.20.30 is capable of retaining solvent vapours (hydrocarbons) permanently up to a filter saturation of more than 99,999%, under normal operating conditions as well as for a simulated accident in the safety storage cabinet.
A special version of the recirculating air filter system UFA.20.30-AUS is also available to meet the pressure conditions and volumetric flows of safety storage cabinets with a small internal volume. It can be installed on a wall bracket or in a convenient housing unit.
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6-Methyl-4-phenylchromanol, 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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Tolterodine Dimer, 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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Fexofenadine, 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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16alpha-Hydroxyprednisolone, 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-Beta-Hydroxybudesonide, 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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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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Rosuvastatin Isoamyl Ester, 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.