Hubei Yuancheng Saichuang Technology Co.,Ltd.

Hubei Yuancheng Saichuang Technology Co.,Ltd.

You are here: HomeProductsIdarubicin hydrochloride

Contact us

  • Company Name: Hubei Yuancheng Saichuang Technology Co.,Ltd.
  • Street: Wuchang
  • City: Wuhan
  • Province/state: Hubei
  • Country/region: China
  • Contact Person: Ms.Merry Zhou
  • Department: Sales
  • Tel: 86-27-50756228
  • Fax: 86-27-88048077
  • Email:

Idarubicin hydrochloride

  • CAS No:57852-57-0 Idarubicin hydrochloride
    Molecular Structure

    Detailed Description

    Idarubicin hydrochloride
    Synonyms:idarubicin hcl;idarubicin hydrochloride;4-demethoxy-daunomycihydrochloride;4-demethoxydaunorubicinhydrochloride;(7s-cis)-9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-5,12-naphthacenedione;4-DMD HCl;5,12-Naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7S,9S)-;5,12-Naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7S-cis)-
    CAS:57852-57-0
    MF:C26H28ClNO9
    MW:533.95
    EINECS:260-990-7
    Chemical Properties:Orange Solid
    Usage:Idarubicin HCl is a hydrochloride salt form of Idarubicin which is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3 ng/mL.Orally active anthracycline; analog of Daunorubicin. Antineoplastic.

    TEST SPECIFICATION RESULT
    Appearance Orange-red crystalline powder; No visible evidence of contamination by foreign matter. Conforms
    Solubility Soluble in water and methanol; slightly soluble in ethanol; practically insoluble in acetone. Conforms
    Identification A The infrared spectrum exhibits maxima only at the same wavelengths as that of a similar preparation of the reference standard. Conforms
    Identification B The chromatogram of the assay preparation obtained in the assay exhibits a major peak for Idarubicin, the retention time of which corresponds to that in the chromatogram of the standard preparation Conforms
    pH 5.0 to 6.5 6.1
    Water Content Not More Than 5.0% 3.6%
    Chromatographic Purity
    Individual Impurity Not More Than 0.2% 0.11%
    Total Impurities Not More Than3.0% 0.7%
    Assay 960 μg to 1030 μg per mg calculated on the anhydrous, solvent-free basis 988μg /mg
    Residual Solvents
    Ethanol Not More Than3000ppm 850ppm
    Methanol Organic Volatile Impurities Methylene Chloride Dioxane Bacterial Endotoxins Not More Than 3000ppm Not More Than 600ppm Not More Than 380ppm Not More Than 8.9 EU/MG 600ppm Not detected Not detected <0.38EU/MG
    Conclusion To be complied with USP 34 specifications
    Ethisterone CAS : 434-03-7
    Norethisterone CAS:68-22-4
    Ethynyl estradiol CAS:57-63-6
    Ethynodiol diacetate CAS:297-76-7
    Chlormadinone acetate CAS.: 302-22-7
    Cyproterone acetate CAS.: 427-51-0
    Megestrol acetate CAS.: 595-33-5
    Estradiol CAS:50-28-2
    17alpha-Oestradiol CAS: 57-91-0
    Estradiol Cypionate CAS:313-06-4
    Estradiol enantate CAS: 4956-37-0
    Estradiol valerate CAS: 979-32-8
    Estradiol Benzoatae CAS:50-50-0
    Estrone CAS: 53-16-7
    Estriol CAS: 50-27-1
    19-Norethindrone acetate CAS:51-98-9
    Norethisterone enanthate CAS:3836-23-5
    Testolactone CAS:968-93-4
    Eplerenone CAS: 107724-20-9
    Progesterone CAS:57-83-0
    Medroxyprogesterone Acetate CAS: 71-58-9
  • Idarubicin hydrochloride
  • Idarubicin hydrochloride