Catalog No.
Product Name
Application
Product Information
Citations
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Drug Impurity
Cetirizine impurity 5 is a known impurity of the antihistamine cetirizine. This compound is primarily relevant in quality control and analytical research, serving as a reference standard to assess the purity and stability of cetirizine formulations. It plays a critical role in the development and validation of analytical methods, ensuring compliance with pharmacological standards in drug manufacturing. -
Drug Impurity
Apixaban impurity 26 is a structural derivative of Apixaban, primarily studied as a drug impurity. This compound is relevant for analytical chemistry and quality control in the development of Apixaban, enabling researchers to assess the purity and stability of the drug. Its presence in formulations can impact pharmacokinetics and safety profiles, making it a crucial component in regulatory assessments. -
Drug Impurity
Flecainide Impurity 3 is a known impurity of the antiarrhythmic agent Flecainide, which primarily targets sodium channels to exert its pharmacological effects. This compound is crucial for quality control in the pharmaceutical industry, allowing researchers to assess the purity and stability of Flecainide formulations. Its identification and quantification are essential for ensuring compliance with regulatory standards in drug development and manufacturing. -
Drug Impurity
Buspirone impurity 4 is a characterized impurity associated with the anxiolytic agent Buspirone. This compound serves as an important reference standard for analytical and quality control applications in pharmaceutical research. Its structural identification and quantification are essential for ensuring the purity and efficacy of Buspirone formulations. -
Drug Impurity
Olmesartan impurity 14 is a compound associated with the synthesis of Olmesartan, a selective angiotensin II receptor antagonist. This impurity is significant in the analysis of pharmaceutical preparations, particularly in quality control and compliance with regulatory standards. It serves as an important reference standard for assessing the purity of Olmesartan formulations in analytical chemistry and drug development research. -
Drug Impurity
Everolimus impurity 10 is a known impurity of the immunosuppressant Everolimus, which targets the mTOR signaling pathway. This impurity is critical for assessing the purity and quality of Everolimus formulations in pharmacological research. It serves as a reference standard in stability studies, quality control, and regulatory compliance for pharmaceutical development. -
Drug Impurity
Rosuvastatin impurity 13 calcium is a chemical impurity associated with Rosuvastatin calcium, which acts as an HMG-CoA reductase inhibitor. This compound is essential for quality control in pharmaceutical formulations, providing insight into the purity and stability of Rosuvastatin products. Researchers utilize this impurity to assess drug formulations and ensure compliance with regulatory standards in therapeutic applications. -
Drug Impurity
Palbociclib impurity 9 is a known impurity of Palbociclib, a selective inhibitor of cyclin-dependent kinases 4 and 6 (CDK4/6). This compound is utilized primarily in the quality control and analytical characterization of Palbociclib, aiding in the assessment of compound purity and efficacy. Its evaluation is essential for ensuring compliance with regulatory standards in pharmaceutical development. -
Drug Impurity
Mirabegron impurity 4 is a chemical impurity associated with the drug Mirabegron, a beta-3 adrenergic receptor agonist. This impurity is important for assessing the purity and quality of Mirabegron formulations in pharmaceutical research. Its characterization is crucial for ensuring compliance with regulatory standards and for conducting stability studies in drug development. -
Pantoprazole Impurity
Pantoprazole N-oxide is a known impurity associated with the synthesis of Pantoprazole, a proton pump inhibitor (PPI) utilized in the treatment of conditions linked to excessive gastric acid, including gastric ulcers and gastroesophageal reflux disease (GERD). This compound is valuable for analytical research and quality control processes, aiding in the characterization and assessment of Pantoprazole formulations. Its presence in pharmaceutical development highlights the importance of monitoring impurities to ensure product safety and efficacy. -
Drug Impurity
Budesonide impurity 90 is a known impurity associated with the corticosteroid Budesonide. This compound serves as an important analytical standard for the characterization and quality control of Budesonide formulations. Researchers can utilize Budesonide impurity 90 in studies focused on the detection and quantification of impurities to ensure compliance with pharmaceutical regulations and to enhance the safety and efficacy profiles of corticosteroid therapies. -
Drug Impurity
Metoprolol impurity 5 is a chemical impurity associated with Metoprolol, a beta-adrenergic blocker. This compound serves as a valuable reference material for quality control and analytical validation in pharmaceutical research, particularly in the development and testing of Metoprolol formulations. Its analysis is crucial for ensuring the purity and safety of Metoprolol-containing products. -
Drug Impurity
Cinacalcet impurity 2 is a chemical impurity associated with the therapeutic agent Cinacalcet. This compound serves as an important reference standard for the analysis and characterization of Cinacalcet formulations. Its presence may be monitored during drug development processes to ensure quality control and compliance with regulatory standards. Researchers can utilize this impurity in various applications, including stability studies and purity assessment in pharmaceutical research. -
Drug Impurity
Tenofovir impurity 7, also known as Tenofovir disoproxil dimer, is a chemical impurity associated with the antiviral drug Tenofovir. This compound is critical for assessing the purity and safety of Tenofovir formulations in pharmaceutical development. It serves as a key reference standard in analytical studies and quality control processes aimed at ensuring compliance with regulatory standards in drug manufacturing. -
Drug Impurity
Rivastigmine impurity 13, also known as Rivastigmine impurity D, is a characterized impurity associated with Rivastigmine, a cholinesterase inhibitor primarily used in the treatment of Alzheimer's disease and other dementias. This impurity may be utilized in quality control and analytical studies to assess the purity and composition of Rivastigmine formulations. Its presence highlights the importance of monitoring drug impurities to ensure safety and efficacy in pharmaceutical products. -
Drug Impurity
Buspirone impurity 1 oxalate is a known impurity associated with the synthesis of Buspirone oxalate. This compound is primarily utilized in the quality control and characterization of Buspirone formulations in pharmaceutical research. Its presence can influence the pharmacological properties of the drug, making it critical for studies focused on drug purity, stability, and efficacy assessments. -
Drug Impurity
Lopinavir impurity 1, also known as Lopinavir impurity K, is a chemical byproduct associated with Lopinavir synthesis. This impurity is important for quality control and characterization in pharmaceutical formulations. It aids researchers in evaluating the purity of Lopinavir products and understanding potential side effects or metabolic pathways in drug development. -
Drug Impurity
Tenofovir impurity 18 is a chemical impurity associated with Tenofovir. It serves as a critical reference standard in the analysis of Tenofovir formulations and aids in assessing the purity and quality of pharmaceutical products. This compound is essential for ensuring compliance with regulatory standards in drug development and quality control processes. -
Drug Impurity
Hydroxychloroquine impurity 5, also known as Hydroxychloroquine O-Sulfate, is a chemical impurity associated with the anti-parasitic compound Hydroxychloroquine. This impurity is of interest in pharmacological research for its potential effects on drug metabolism and safety profiling. Its characterization is essential for ensuring the quality and efficacy of Hydroxychloroquine formulations. -
Drug Impurity
Albendazole impurity 5 is a chemical impurity associated with the antiparasitic agent Albendazole. This compound is utilized in the quality control and characterization of Albendazole formulations. Its presence may impact the safety and efficacy of drug products, making it essential for pharmaceutical research and development. -
Terbutaline Impurity
(4RS)-2-(1,1-Dimethylethyl)-1,2,3,4-tetrahydroisoquinoline-4,6,8-triol hemisulfate is a known impurity of Terbutaline. This compound may serve as a reference standard in analytical chemistry for ensuring the purity of Terbutaline formulations. Its presence can be crucial for the quality control of pharmaceutical products, aiding in the development and validation of analytical methods. -
Drug Impurity
Bupropion impurity 1, also known as (S)-Bupropion, is a structural impurity associated with the pharmaceutical compound Bupropion. It is relevant in pharmaceutical research for studying the potential effects and safety profiles of drug formulations. This impurity can also assist in understanding metabolic pathways and elucidating the therapeutic activity of Bupropion in clinical applications. -
Drug Impurity
Hydrocortisone acetate impurity 2 is a chemically defined impurity derived from hydrocortisone acetate. This compound serves as an important reference standard in the assessment of drug quality and formulation. Its examination is critical for understanding the impurity profile during hydrocortisone acetate synthesis and ensuring the safety and efficacy of pharmaceutical products. This impurity is also valuable for analytical development and regulatory compliance in the pharmaceutical industry. -
Drug Impurity
Afatinib impurity 92 is a byproduct of Afatinib, a potent irreversible inhibitor of the epidermal growth factor receptor (EGFR) tyrosine kinase. This impurity is essential for quality control and characterization in pharmaceutical research and development, ensuring the purity and efficacy of EGFR-targeted therapies. It serves as a crucial component for analytical studies, providing insights into potential degradation pathways and stability assessment of Afatinib formulations. -
Drug Impurity
Linagliptin impurity 87 is a known impurity associated with Linagliptin, a selective DPP-4 inhibitor. This impurity is critical for the assessment of drug purity and quality in pharmaceutical development. Its analysis is important for ensuring compliance with regulatory standards in drug formulation and safety evaluations. -
Drug Impurity
Amoxicillin Impurity 6 is an impurity associated with Amoxicillin, a widely used beta-lactam antibiotic. This compound is valuable for quality control and analytical research in pharmaceutical development, aiding in the identification and characterization of drug impurities. Its study supports the assessment of drug purity and helps ensure compliance with regulatory standards in the manufacturing processes of antibiotics. -
Drug Impurity
Fusidic acid impurity 7 is a chemical impurity associated with fusidic acid. This compound serves as a critical reference standard for assessing the purity and quality of fusidic acid formulations. Its identification and quantification are essential in pharmaceutical research to ensure compliance with regulatory standards and to evaluate the safety and efficacy of drug products containing fusidic acid. -
Drug Impurity
Raloxifene impurity 6 is a known impurity of the selective estrogen receptor modulator, Raloxifene. This compound is utilized primarily in the evaluation of drug purity and the assessment of Raloxifene formulations in pharmaceutical development. Understanding its characteristics is essential for ensuring the quality and safety of therapeutic agents containing Raloxifene. -
Drug Impurity
Tamsulosin impurity 2 is an impurity associated with the drug Tamsulosin, primarily utilized in the treatment of benign prostatic hyperplasia. Its presence in formulations is critical for quality control and regulatory compliance. This reagent is valuable for analytical research and method development in pharmaceutical studies focusing on the safety and efficacy of Tamsulosin products. -
Drug Impurity
Aripiprazole impurity 7 is a known impurity associated with Aripiprazole. This compound serves as a useful reference standard in the development, quality control, and stability testing of pharmaceutical formulations containing Aripiprazole. Its identification and analysis can aid in ensuring the safety and efficacy of the drug in clinical applications. Researchers may utilize this impurity for analytical purposes in compliance with regulatory standards. -
Drug Impurity
Acyclovir impurity 7 is a known impurity of the antiviral agent Acyclovir. It is utilized primarily in drug quality control and analytical studies to ensure the purity and efficacy of pharmaceutical formulations. Research applications include assessing the stability, degradation pathways, and overall integrity of Acyclovir-related compounds in drug development processes. -
Drug Impurity
Rosuvastatin impurity 34 is a known impurity associated with the statin drug Rosuvastatin. This compound is primarily used for analytical and quality control applications in pharmaceutical research, particularly for the assessment of drug purity and stability. Its identification and quantification are essential for ensuring the safety and efficacy of Rosuvastatin formulations in clinical settings. -
Drug Impurity
Rosuvastatin impurity 43 is a known impurity of Rosuvastatin, a statin used for lowering cholesterol levels. This compound is critical in drug development and quality control for assessing the purity of Rosuvastatin formulations. Its identification and quantification are essential in ensuring the safety and efficacy of statin-based therapies. Research applications include method development for impurity analysis and stability testing. -
Drug Intermediate
PDE4 inhibitor intermediate 1 serves as a key building block in the synthesis of phosphodiesterase 4 (PDE4) inhibitors. This compound is crucial in the development of therapeutics aimed at modulating inflammatory responses and is particularly relevant in the study of respiratory diseases and neurodegenerative disorders. Its role as an intermediate facilitates the exploration of various PDE4 inhibition strategies in pharmacological research. -
Biochemical Reagent
NAD(P)H-Nitrate reductase is a biochemical reagent derived from Aspergillus niger, facilitating the reduction of nitrate to nitrite through a two-electron transfer mechanism. This enzyme utilizes NADPH as an electron donor, functioning as a bispecific NAD(P)H:Nitrate reductase. It is essential for studies involving nitrogen metabolism, enzymatic activity assays, and the exploration of metabolic pathways in both plant and microbial systems. -
Biochemical Assay Reagent
Fluo-3 ammonium is a cell-impermeable calcium ion (Ca2+) indicator that fluoresces upon binding to calcium ions, with excitation and emission wavelengths of 488 nm and 525 nm, respectively. This reagent is primarily used in biochemical assays to monitor intracellular calcium levels, providing valuable insights into calcium-mediated signaling pathways. Its ability to selectively respond to Ca2+ makes Fluo-3 ammonium an essential tool for researchers investigating cellular processes related to calcium dynamics. -
Biochemical Assay Reagent
Driselase, derived from Basidiomycetes sp., is a complex mixture of wall-digesting enzymes primarily used as a biochemical assay reagent. It effectively promotes protoplast formation in fungi when combined with lyase, facilitating advanced studies in fungal physiology and genetics. Driselase demonstrates exceptional potency in polysaccharide digestion, enhancing both tensile and indentation compliances without inducing wall creep, even after extended digestion periods. This makes it an invaluable tool for researchers investigating cell wall dynamics and protoplast isolation. -
Biochemical Reagent
Benzoylacetone, also known as 1-Phenylbutane-1,3-dione, is a biochemical reagent primarily utilized in organic synthesis and analytical chemistry. This compound exhibits diverse biological activities, including chelation of metal ions and influence on enzyme activity, making it valuable in various research applications. It is commonly employed in studies related to drug development, fluorescence detection, and the investigation of biological pathways. -
Biochemical Assay Reagent
rel-Biotin methyl ester is a biochemical reagent utilized for its role as a biotinylation agent in various molecular biology applications. This compound functions as a derivative of biotin, facilitating the study of protein interactions, labeling, and detection in biochemical assays. Its use is critical in the development of affinity purification techniques, ensuring accurate analysis in life science research. -
Biochemical Assay Reagent
N-Biotinyl-1,6-hexanediaMine is a biotinylated compound designed for use in biochemical assays. It facilitates the study of protein interactions and cellular processes by serving as a tag for proteins, enabling their detection and isolation. This reagent is essential for applications in proteomics, molecular biology, and various life science research endeavors. -
Biochemical Assay Reagent
2,5-Dioxopyrrolidin-1-yl 4-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)butanoate is a specialized biotinylation reagent featuring a terminal NHS ester, enabling selective and efficient conjugation to amine-containing biomolecules. This compound is widely utilized in biochemical assays for labeling proteins, peptides, and other amine substrates, facilitating studies in protein interactions, cellular uptake, and targeted drug delivery. Its high specificity enhances experimental outcomes in various research applications, including proteomics and biomolecular imaging. -
Camphor impurity
Isopropyl (1S)-(+)-10-camphorsulfate is identified as an impurity of camphor, a compound recognized for its topical anti-infective and anti-pruritic properties, as well as its efficacy as a stimulant and carminative when administered internally. This impurity serves as a critical reference point for researchers studying the safety and efficacy of camphor and its derivatives in various biological applications, including pharmacological investigations and formulation developments. -
Biochemical Assay Reagent Control
Chlorotriethylsilane is a reagent commonly used in biochemical assays as a versatile control agent. It serves as a silylating agent, facilitating the derivatization of functional groups for enhanced detection and analysis in various chemical reactions. Its key applications include sample preparation, chromatographic analysis, and the development of novel analytical methods in chemical research. -
Biochemical Reagent
Potassium iodide is a biochemical reagent primarily used in various life science research applications. It serves as a source of iodide ions and is utilized in assays, such as thyroid function tests and imaging studies. Additionally, potassium iodide exhibits antioxidant properties and can impact cell signaling pathways, making it valuable for studies involving cellular responses and biochemical mechanisms. -
Biochemical Reagent
5-Methylfurfural is an organic compound that serves as a biochemical reagent with diverse applications in research. It is a key intermediate in the production of agrochemicals and is also utilized as a precursor for certain anti-cancer natural products. Additionally, 5-Methylfurfural is known to induce skin inflammation and disrupt the skin barrier, along with its ability to degrade native DNA by causing single-strand breaks. Its potential for further hydrogenation to 2,5-dimethylfuran (DMF) also highlights its relevance in synthetic chemistry studies. -
Drug Intermediate
2'-Hydroxyacetophenone is a versatile chemical intermediate widely used in the synthesis of various pharmaceuticals. This compound possesses notable flavoring properties, making it relevant in the food and beverage industry. It is also utilized in the preparation of multiple organic compounds, providing a significant role in chemical research and development applications. -
Biochemical Reagent
4-(1H-Pyrazol-4-yl)-7-[[2-(trimethylsilyl)ethoxy]methyl]-7H-pyrrolo[2,3-d]pyrimidine functions as a biochemical reagent, specifically designed for life sciences research. Its unique structural properties allow it to participate in various biological assays and syntheses. This compound demonstrates potential for exploring enzyme kinetics, signaling pathways, and other molecular interactions pertinent to drug discovery and development. -
Biochemical Reagent
PD 128907 hydrochloride is a biochemical reagent primarily utilized in life science research. It serves as a key tool for studying various biological processes and mechanisms. This compound can be employed in a range of experimental applications, particularly in the exploration of cellular signaling pathways and related biochemical activities. -
Biochemical Reagent
Disodium monofluorophosphate is a biochemical reagent that functions primarily as a phosphate donor. It exhibits biological activity by influencing various enzyme interactions and metabolic pathways, making it valuable in enzymatic studies. This compound is commonly utilized in life sciences research, particularly in investigations involving phosphate metabolism and the role of phosphatases. -
Biochemical Reagent
Lithium carbonate is a biochemical reagent primarily utilized in the research of mood stabilization mechanisms. It acts on various neurotransmitter systems, influencing levels of serotonin and norepinephrine, making it relevant for studies on bipolar disorder and depression. This compound is integral for exploring neurochemical pathways and evaluating potential therapeutic applications in psychiatric disorders.
