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10048 results for Organic Standards

You searched for: Organic Standards

Avantor offers a wide range of certified organic standards designed for instrument calibration in ion-exchange chromatography (IC) applications, which can be applied toward environmental or food analysis and quality control. IC is an analytical technique used for the separation and quantification of anions and cations in aqueous samples. Avantor offers high-purity, well-defined reference materials ideal for low-ppm level quantification or trace analysis. Bottles of organic standards are available for a range of elements.

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beta-Apo-oxytetracycline, can be used as secondary standard

beta-Apo-oxytetracycline, can be used as secondary standard

Supplier: Thermo Fisher Scientific

CAS No.: 18751-99-0

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Abacavir, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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NMPH Solution (1 ml (1 mg/ml)) (Methyl 2-(1-nitrosopiperidin-2-yl)-2-phenylacetate), Pharmaceutical Analytical Impurities

Supplier: USP

Organic Standard, N-Nitrosomethylphenidate (NMPH) solution (1 ml (1 mg/ml)) (Methyl 2-(1-nitrosopiperidin-2-yl)-2-phenylacetate)

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Atorvastatin Ethyl 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.

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Acamprosate Calcium, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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Abiraterone Acetate, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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Abacavir Sulfate, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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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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Isobutylglutarmonoamide, 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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Anhydrotetracycline hydrochloride, can be used as a secondary standard

Anhydrotetracycline hydrochloride, can be used as a secondary standard

Supplier: Thermo Fisher Scientific

Purity: ≥80 % (as is, calculated)

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Glyceryl Monooleate, Reference Standards

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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Fluphenazine Decanoate Dihydrochloride, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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Acetaminophen Related Compounds, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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Desmethoxy Omeprazole, 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-Isopropyl Carvedilol, 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-Acetyl 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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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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Tolyloyl Bromopropionamide, 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-Epichlortetracycline hydrochloride, 97%, can be used as secondary standard

4-Epichlortetracycline hydrochloride, 97%, can be used as secondary standard

Supplier: Thermo Fisher Scientific

Organic Standard, 4-Epichlortetracycline hydrochloride, Pack type: Glass bottle

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Oleoyl Polyoxylglycerides, Reference Standard

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

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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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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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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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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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Rivaroxaban Desthiophene 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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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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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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