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You Searched For: Tenofovir+disoproxil+fumarate

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Tenofovir disoproxil fumarate 98%

Supplier: Thermo Scientific

Description: Tenofovir disoproxil fumarate 98%

Tenofovir disoproxil fumarate ≥98%, crystalline solid

Supplier: Cayman Chemical

Description: Tenofovir disoproxil is a prodrug of the acyclic nucleoside phosphonate, tenofovir. Tenofovir is converted by cellular enzymes to tenofovir diphosphate, an obligate chain terminator that inhibits the activity of HIV reverse transcriptase and hepatitis B virus polymerase. Due to its rapid intracellular uptake, the anti-HIV activity of tenofovir disoproxil is reportedly >100-fold greater than that of the negatively charged tenofovir in a T cell line and primary blood lymphocytes.

Tenofovir Disoproxil Fumarate, Reference Standard

Catalog Number: (1643656.)

Supplier: USP

Description: 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.

UOM: 1 * 200 mg

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N/A Each

Impurity and API standard, tenofovir disoproxil fumarate

Catalog Number: (PROOMM1329.00)

Supplier: LGC Standards PROMOCHEM

Description: Organic Standard, Tenofovir disoproxil fumarate

UOM: 1 * 100 mg

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N/A Each

Tenofovir Related Compounds, Reference Standard

Supplier: USP

Tenofovir, Reference Standard

Catalog Number: (1643601.)

Supplier: USP

Description: USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. 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.

UOM: 1 * 15 mg

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