Found: 12
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Eco-friendly and green chromatographic method for the simultaneous determination of chlorocresol and betamethasone dipropionate in topical formulations using Box–Behnken design.
- Published in:
- Journal of the Iranian Chemical Society, 2022, v. 19, n. 4, p. 1397, doi. 10.1007/s13738-021-02388-5
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- Article
Reverse-phase LC method development and validation for the quantification of acetazolamide and its specified and unspecified degradation products in hard gelatin capsule formulations.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 3, p. 775, doi. 10.1007/s13738-021-02341-6
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- Article
Quantitative estimation of Fulvestrant injection 505(j) composition and impurities profile by capillary gas chromatography and HPLC-PDA techniques.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 6, p. 1443, doi. 10.1007/s13738-020-02126-3
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- Article
A validated stability‐indicating reversed‐phase‐HPLC method for dipyridamole in the presence of degradation products and its process‐related impurities in pharmaceutical dosage forms.
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- Biomedical Chromatography, 2022, v. 36, n. 1, p. 1, doi. 10.1002/bmc.5247
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- Article
Development and validation of a stability‐indicating UPLC method for the determination of olmesartan medoxomil, amlodipine and hydrochlorothiazide degradation impurities in their triple‐combination dosage form using factorial design of experiments
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- Biomedical Chromatography, 2021, v. 35, n. 11, p. 1, doi. 10.1002/bmc.5194
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- Article
Development and validation of LC–MS method for the determination of heptaethylene glycol monomethyl ether in benzonatate bulk drugs.
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- Biomedical Chromatography, 2021, v. 35, n. 7, p. 1, doi. 10.1002/bmc.5096
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- Article
Low‐level determination of 4‐chlorobutyl‐(S)‐[4‐chloro‐2‐(4‐cyclopropyl‐1,1,1‐trifluoro‐2‐hydroxy‐but‐3yn‐2‐yl)phenyl] carbamate (4‐CTHC) in efavirenz drug substance by LC–MS
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- Biomedical Chromatography, 2021, v. 35, n. 7, p. 1, doi. 10.1002/bmc.5086
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- Article
Oxidative degradation profile studies of tavaborole by a validated stability indicating RP‐UPLC method: Isolation and characterization of novel degradant using 2D‐NMR and HRMS.
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- Biomedical Chromatography, 2021, v. 35, n. 6, p. 1, doi. 10.1002/bmc.5070
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- Article
Novel reversed‐phase HPLC method for simultaneous determination of ethynodiol diacetate (EDA)/ethinyl estradiol (EE) in pharmaceutical dosage form.
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- Biomedical Chromatography, 2021, v. 35, n. 5, p. 1, doi. 10.1002/bmc.5055
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- Article
Development and validation of rapid ultra high performance liquid chromatography with tandem mass spectroscopic method for the quantification of N‐nitrosodimethyl amine and N‐nitrosodiethyl amine in sitagliptin and metformin hydrochloride immediate and extended‐release formulations
- Published in:
- Journal of Separation Science, 2022, v. 45, n. 16, p. 3067, doi. 10.1002/jssc.202200226
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- Article
An Improved Process for the Enantioselective Synthesis of HCV NS5A Inhibitor Elbasvir (MK-8742) Chiral Amine Intermediate.
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- Russian Journal of General Chemistry, 2021, v. 91, n. 5, p. 932, doi. 10.1134/S107036322105025X
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- Article
AQbD based green UPLC method to determine mycophenolate mofetil impurities and Identification of degradation products by QToF LCMS.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-22998-0
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- Article