Tenofovir

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Hydroxy methyl Tenofovir Disoproxil

  • CAT Number DCTI-C-046
  • CAS Number 1244022-53-4
  • Molecular Formula C20H32N5O11P
  • Molecular Weight 549.47

Hydroxy Methyl Tenofovir Monoproxil

  • CAT Number DCTI-C-181
  • CAS Number 1244022-55-6
  • Molecular Formula C15H24N5O8P
  • Molecular Weight 433.36

Isopropyl impurity of Tenofovir Di ethyl amine salt

  • CAT Number DCTI-C-1069
  • CAS Number NA
  • Molecular Formula C18H28N5O9P (Free Base) C22H39N6O9P(Diethyl amine Salt)
  • Molecular Weight 489.14 (Free Base) 562.25 (Diethyl amine Salt)

Isopropyl impurity of Tenofovir diethylamine salt

  • CAT Number DCTI-C-1607
  • CAS Number 1244022-56-7 (Free acid)
  • Molecular Formula C18H28N5O8P (Free acid) C22H39N6O8P (Diethylamine Base)
  • Molecular Weight 489.14 (Free acid) 562.25 (Diethylamine salt)

Isopropyl Tenofovir

  • CAT Number DCTI-C-835
  • CAS Number NA
  • Molecular Formula C12H20N5O4P (Free Base) C12H23N6O4P (Ammonium Salt)
  • Molecular Weight 329.30 (Free Base) 346.33 (Ammonium Salt)

Phenyl hydrogen ((((R )-1-(6-amino-9H-purin-9-yl)-...

  • CAT Number DCTI-C-397
  • CAS Number 379270-35-6
  • Molecular Formula C15H18N5O4P
  • Molecular Weight 363.31

PMPA Mono Ester Impurity

  • CAT Number DCTI-C-834
  • CAS Number NA
  • Molecular Formula C11H18N5O4P (Free Base) C11H21N6O4P (Ammonium Salt)
  • Molecular Weight 315.27 (Free Base) 332.30 (Ammonium Salt)

PMPA Propyl Ester Impurity

  • CAT Number DCTI-C-964
  • CAS Number NA
  • Molecular Formula C12H20N5O4P (Free Base) C12H23N6O4P (Ammonium Salt)
  • Molecular Weight 329.30 (Free Base) 346.33 (Ammonium Salt)

S-Tenofovir Disoproxil Fumarate

  • CAT Number DCTI-C-089
  • CAS Number 1432630-26-6
  • Molecular Formula C23H34N5O14P (Fumerate Salt) C19H30N5O10P (Free base)
  • Molecular Weight 635.52 (Fumerate Salt) 519.45 (Free base)
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References
FAQ's

Frequently Asked Questions

The impurities typically found in Tenofovir include related substances, such as process-related impurities and degradation products.

The impurities in Tenofovir are analyzed using high-performance liquid chromatography (HPLC), which separates the impurities from the drug substance and quantifies their concentrations.

The impurities in Tenofovir are removed, through various purification methods, such as crystallization and column chromatography. The extent to which the removal of impurities depends on their chemical properties and concentration.

Tenofovir impurities are stored at a controlled room temperature between 2-8 °C or as indicated on the Certificate of Analysis (CoA).

Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.

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