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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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Fluoro Risperidone, 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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Acebutolol Hydrochloride, 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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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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VWR® PESTINORM®, GC Multiresidue Pesticide Standard (Mix 3) - 25 components, CRM

VWR® PESTINORM®, GC Multiresidue Pesticide Standard (Mix 3) - 25 components, CRM

Supplier: VWR Chemicals

A standard mixture, typically used for food testing, containing the following components: 100 ug/ml each of Benfluralin [CAS:1861-40-1] ; Biphenyl [CAS:92-52-4] ; Chlorothalonil [CAS:1897-45-6] ; Dichlofluanid [CAS:1085-98-9] ; Dicloran [CAS:99-30-9] ; 3,4-Dichloroaniline [CAS:95-76-1] ; Dichlobenil [CAS:1194-65-6] ; Diphenylamine [CAS:122-39-4] ; Ethalfluralin [CAS:55283-68-6] ; Fluchloralin [CAS:33245-39-5] ; Isopropalin [CAS:33820-53-0] ; Nitralin [CAS:4726-14-1] ; Nitrofen [CAS:1836-75-5] ; Oxyfluorfen [CAS:42874-03-3] ; Pendimethalin [CAS:40487-42-1] ; Pentachloroaniline [CAS:527-20-8] ; Pentachlorobenzonitrile [CAS:20925-85-3] ; Quintozene [CAS:82-68-8] ; Prodiamine [CAS:29091-21-2] ; Profluralin [CAS:26399-36-0] ; 2,3,5,6-Tetrachloroaniline [CAS:3481-20-7] ; Tecnazene [CAS:117-18-0] ; cis-1,2,3,6-Tetrahydrophthalimide [CAS:1469-48-3] ; Tolylfluanid [CAS:731-27-1] ; Trifluralin [CAS:1582-09-8] in Toluene / Acetonitrile (99/1)

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Behenoyl 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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Acetone, 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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Albuterol 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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Latanoprost 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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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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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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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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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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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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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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Duloxetine Related Compounds, 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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Abiraterone System Suitability Mixtures, 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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Acarbose System Suitability Mixtures, 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 System Suitability Mixtures, 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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Budesonide Pyruvic 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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17-Oxo Dexamethasone, 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 D-homo 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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Amlodipine Besylate, 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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Amlodipine 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(dibenzothiazepinyl) Piperazine, 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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Lacosamide, 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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Pemetrexed Glutamide, 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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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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Nevirapine 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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