Catalog No.
Product Name
Application
Product Information
Citations
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Metal-organic Framework
3,5-Bis(trifluoromethyl)-4H-1,2,4-triazole serves as a key building block for the synthesis of metal-organic frameworks (MOFs). Its unique trifluoromethyl groups enhance the stability and porosity of the framework, making it suitable for applications in gas storage, catalysis, and separation processes. This compound is valuable for researchers exploring advanced materials in the fields of chemistry and materials science. -
Biochemical Reagent
4-(Hydroxymethyl)benzoic acid is a biochemical reagent utilized primarily for various life science applications. Its functional groups facilitate interactions with biological molecules, making it useful in studies involving enzyme activity, molecular recognition, and metabolic pathways. This compound serves as an essential building block in the synthesis of other biochemical agents and aids in the exploration of cellular processes. -
Biochemical Reagent
2,3-Dihydroxynaphthalene is a biochemical reagent that serves as a valuable organic compound for life science research. It exhibits antioxidant properties and may be utilized in studies related to enzymatic reactions, metabolic pathways, and the investigation of phenolic compounds. This compound is relevant for researchers examining the biochemical interactions of naphthalene derivatives in various biological systems. -
Biochemical Assay Reagent
Lead carbonate(II) serves as a biochemical assay reagent primarily utilized for various analytical applications in biological research. This compound exhibits properties that facilitate the quantitative assessment of biomolecules in solution, aiding in the study of their interactions and functions. Its utility in assays makes it an essential tool for researchers investigating biochemical pathways and the effects of various compounds in cellular environments. -
Biochemical Assay Reagent
2-Ethoxyphenol, primarily utilized as a biochemical assay reagent, features a phenolic ring substituted with an ethoxy group at the 2-position. This compound exhibits notable antioxidant properties and is often employed in biochemical assays to study enzymatic activities and phenolic compounds. Its utility extends to research involving flavor compounds and their interactions in food chemistry. -
Biochemical Reagent
3-Hydroxy-4-nitrobenzoic acid is a biochemical reagent with applications in life science research. It serves as a key organic compound that can be utilized in various biochemical assays and studies involving enzymatic and metabolic pathways. Its utility in biochemical investigations makes it an important tool for researchers exploring cellular mechanisms and organic synthesis. -
Drug Derivative
5′-Fluoro-5′-deoxyadenosine is a nucleoside analog that primarily targets adenosine metabolism. It exhibits antiviral and anticancer properties, making it valuable for research applications in pharmacology and molecular biology. This compound is utilized in studies exploring nucleotide synthesis and the development of novel therapeutic strategies. -
Biochemical Assay Reagent
5β-Cholestane serves as a biochemical assay reagent primarily utilized in life science research. This organic compound plays a significant role in studying cholesterol metabolism and related pathways. Its applications include serving as a reference material for analytical methods and facilitating investigations into sterol biology. -
Ester Product
10-Undecenyl acetate is an ester compound commonly utilized in organic synthesis. This reagent serves as a versatile building block in the preparation of various chemical entities. Its chemical structure makes it particularly useful in studies involving lipid chemistry and the synthesis of surfactants, fragrances, and other organic materials. 10-Undecenyl acetate's unique properties facilitate research applications in biochemistry and chemical biology. -
Biochemical Assay Reagent
Palmityl acetate is an ester compound primarily used as a biochemical assay reagent. It exhibits lubricating and emollient properties, making it suitable for applications in cosmetic formulations and personal care products. Additionally, palmityl acetate functions as a plasticizer and stabilizer in plastics and resins, contributing to the performance of various commercial goods, including perfumes, lotions, and hair care products. Its versatile chemical characteristics facilitate a wide range of research applications in the field of biochemistry. -
Biochemical Reagent
Benzhydrol, also known as diphenylmethanol, serves as a biochemical reagent applicable in various life science research contexts. Its chemical properties enable it to function as a versatile organic compound, facilitating studies related to synthetic organic chemistry and biochemistry. Utilized in drug formulation and synthesis, Benzhydrol is pivotal for investigations into molecular interactions and mechanisms within biological systems. -
Biochemical Reagent
3,5-Di(trifluoromethyl)aniline is a biochemical reagent that functions primarily as a versatile organic compound. This compound exhibits significant utility in various life science research applications, including biochemical studies and organic synthesis. Its unique trifluoromethyl groups enhance its reactivity and solubility, making it valuable for investigating biochemical pathways and developing new chemical entities. -
Biochemical Reagent
3-Butyn-1-ol is a biochemical reagent functioning primarily as an alkyne-derived compound in click chemistry applications. Its reactive alkyne group enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. This versatility makes 3-Butyn-1-ol an essential tool in chemical biology, facilitating bioconjugation and the development of complex biomolecular architectures. -
Biochemical Reagent
1,3-Propanediyl bismethanethiosulfonate is a biochemical reagent that primarily targets sulfhydryl groups in proteins and peptides, facilitating the formation of disulfide bonds. This compound is utilized in biochemical research for the study of protein structure and function, as well as in the development of novel therapeutic agents. Its ability to modify cysteine residues makes it valuable in diverse applications, including enzyme inhibition studies and the synthesis of thiol-reactive probes. -
Drug Derivative
MARY15 is a pyridinylpiperazine-derived compound that primarily targets mitochondrial respiration. This reagent promotes uncoupled mitochondrial respiration and effectively enhances p-AKT (S473) phosphorylation in renal proximal tubule cells. MARY15 is valuable for research on metabolic regulation and signal transduction pathways associated with kidney function. -
Drug Derivative
Flufenamic acid glucuronide is an acyl-linked glucuronide derivative of Flufenamic acid. This compound is instrumental in studying acyl glucuronide rearrangement and contributes to understanding drug metabolism pathways. Its role in pharmacokinetics and potential metabolic transformations makes it a valuable reagent for chemical research in drug development and safety assessments. -
Nitrosamine Drug Substance-Related Impurity
N-Nitrosovancomycin is a nitrosamine drug substance-related impurity (NDSRI) associated with vancomycin hydrochloride. This compound is of particular interest in pharmaceutical research due to its relevance in drug safety assessments and regulatory compliance. Its presence can provide insights into the stability and degradation pathways of vancomycin in various formulations. -
Biochemical Assay Reagent
Chloro(methyl)(phenyl)silane is a silicon hydride that acts as a biochemical assay reagent. It demonstrates the ability to participate in addition reactions with long-chain unsaturated fatty acid esters, making it valuable for synthetic applications in organic chemistry. Its utility in the modification of various substrates supports a wide range of research applications in chemical biology and materials science. -
Drug Impurity
Atenolol impurity 8 is a structural impurity associated with Atenolol, a selective beta-1 adrenergic receptor blocker. This compound is crucial for analyzing the purity of Atenolol formulations and evaluating potential impacts on drug efficacy and safety. It serves as an important reference standard in the pharmaceutical industry for quality control and compliance in drug development and analysis. -
Drug Impurity
Ranolazine impurity 3 is a chemical impurity associated with Ranolazine, primarily used as a reference standard in analytical and quality control applications. This compound is essential for ensuring the purity and consistency of Ranolazine formulations. Its characterization contributes to the understanding of metabolic pathways and the identification of potential degradation products. Research involving this impurity aids in enhancing the quality of pharmaceutical formulations and supports regulatory compliance in drug development processes. -
Drug Impurity
Olmesartan impurity 1 serves as a structural impurity related to the antihypertensive agent Olmesartan. This compound is essential for the analytical characterization of Olmesartan, particularly in the context of quality control and regulatory compliance in pharmaceutical development. Its presence and quantification can provide insights into the synthesis purity and stability profiles of Olmesartan formulations. -
Drug Impurity
Rivaroxaban impurity 67 is a defined impurity of the anticoagulant Rivaroxaban. This compound serves as a critical reference standard for analytical and quality control processes in the pharmaceutical industry. It aids in routine testing, stability analysis, and ensuring the purity of Rivaroxaban formulations in drug development and regulatory compliance. -
Drug Impurity
Cabozantinib impurity 7 is a synthetic impurity derivative of the tyrosine kinase inhibitor Cabozantinib. It serves as a crucial reference standard for quality control and analytical studies related to Cabozantinib production. This compound aids in the characterization and assessment of drug purity, essential for pharmacokinetics and toxicological research applications. -
Drug Impurity
Estradiol impurity 1 is a known impurity associated with the synthesis of Estradiol. This compound can serve as a critical reference for assessing the purity of Estradiol formulations in research and quality control applications. It is important for researchers studying the metabolism and pharmacokinetics of estrogenic compounds, as well as in the evaluation of drug safety and efficacy. -
Drug Intermediate
(1R,3S)-3-Hydroxycyclopentane carboxylic acid methyl ester serves as a valuable synthetic intermediate in pharmaceutical synthesis. This compound can facilitate the development of bioactive molecules and various drug formulations. Its unique structure aids in the exploration of novel therapeutic agents, making it an essential reagent for research in medicinal chemistry. -
Drug Impurity
Lifitegrast impurity 4 hydrochloride is a chemical impurity associated with Lifitegrast, primarily known for its role as a lymphocyte function-associated antigen-1 (LFA-1) antagonist. This impurity serves as a reference standard for analytical characterization and quality control in pharmacological studies of Lifitegrast. Research applications include assessing the purity of the active pharmaceutical ingredient and evaluating potential effects on drug efficacy and safety profiles. -
Drug Impurity
Sitagliptin impurity 25 is a known impurity associated with the DPP-4 inhibitor Sitagliptin, primarily targeting the Dipeptidyl Peptidase-4 enzyme. This compound is essential for quality control in the synthesis and analysis of Sitagliptin and is relevant for pharmacokinetic and toxicological studies. Its characterization supports research into drug formulation and regulatory compliance. -
Drug Impurity
Tamsulosin Impurity 6 serves as a drug impurity associated with the pharmaceutical compound tamsulosin. Its presence is critical for quality control and regulatory compliance during the manufacturing process. This compound is utilized in research applications to investigate the safety and efficacy of tamsulosin formulations, contributing to the understanding of potential impacts on drug performance and stability. -
Drug Impurity
Donepezil impurity 10 is a known impurity associated with the compound Donepezil, a reversible inhibitor of the enzyme acetylcholinesterase. This reagent is significant for analytical studies aimed at monitoring the purity of Donepezil in pharmaceutical formulations. It serves as a reference standard in quality control processes and method development, ensuring compliance with regulatory guidelines in drug manufacturing and research applications. -
Drug Impurity
Apixaban 4,5-dehydro carboxylic acid is a known drug impurity of Apixaban, an anticoagulant that functions primarily by inhibiting Factor Xa in the coagulation cascade. This compound serves as an important reference standard for analytical and stability studies in pharmaceutical development. Research applications include the assessment of drug purity, identification of degradation products, and evaluation of manufacturing processes. -
Drug Impurity
Tamsulosin impurity 21 is a chemical impurity associated with the drug Tamsulosin, which primarily targets the α1-adrenergic receptors. This impurity may serve as a valuable reference standard in the analysis of Tamsulosin formulations. Its identification is crucial for assessing the purity and quality of pharmaceutical products in drug development and quality control. -
Drug Impurity
Ramipril impurity 3 is a minor impurity associated with the angiotensin-converting enzyme (ACE) inhibitor Ramipril. This compound serves as a reference standard in the analysis of Ramipril for quality control and pharmaceutical research applications. Investigating impurities like Ramipril impurity 3 is essential for understanding the compound's safety profile and ensuring compliance with regulatory standards. -
Drug Impurity
Terbinafine impurity 13 is a known impurity associated with the antifungal agent Terbinafine. This compound serves as a reference standard for analytical studies and quality control in pharmaceutical formulations. Its characterization and quantification are essential for ensuring the purity and efficacy of Terbinafine in drug development and regulatory processes. -
Drug Impurity
Vildagliptin impurity 24 is a chemical impurity associated with the antidiabetic agent Vildagliptin. This impurity is crucial for analytical and quality control applications in pharmaceutical research and development. Its identification and quantification are essential for assessing the purity of Vildagliptin and ensuring the safety and efficacy of formulations containing this compound. -
Drug Impurity
Telmisartan impurity 5 (2-Boc-4'-(bromomethyl)biphenyl) is a characterized impurity associated with Telmisartan, an antihypertensive agent. It serves as a reference standard for quality control and analytical testing in pharmaceutical development. The presence and quantification of this impurity are crucial for assessing the purity and safety profiles of Telmisartan formulations. -
Drug Impurity
Escitalopram impurity 7 oxalate, also known as 3-Hydroxy citalopram oxalate, is a drug impurity associated with Escitalopram oxalate. This compound is utilized in pharmaceutical research and development to assess the purity and stability of escitalopram formulations. Its analysis is critical for ensuring compliance with regulatory standards and understanding the pharmacokinetic profile of the parent drug. -
Drug Impurity
Sitagliptin impurity 1 is a known impurity associated with the drug Sitagliptin, an inhibitor of the Dipeptidyl Peptidase-4 (DPP-4) enzyme. This compound is utilized primarily for quality control and analytical purposes in pharmaceutical research, ensuring the purity and safety of Sitagliptin formulations. It plays a critical role in the development and validation of quality assurance protocols in drug manufacturing. -
Drug Impurity
Montelukast impurity 14 is a chemical compound associated with the synthesis of Montelukast, specifically categorized as a drug impurity. This impurity can be used in analytical chemistry to assess the purity of Montelukast formulations and contribute to quality control processes. Its detection and quantification are essential for ensuring compliance with regulatory standards in pharmaceutical development and manufacturing. -
Drug Impurity
Terbinafine impurity 5 is a chemical impurity associated with the antifungal agent Terbinafine. It is primarily utilized in the analysis of drug formulations and quality control assessments to ensure the purity of pharmaceutical products. This impurity serves as an essential reference standard in stability testing and the development of analytical methods in pharmaceutical research. -
Drug Impurity
Sertraline impurity 5 is a chemical impurity associated with the selective serotonin reuptake inhibitor (SSRI) Sertraline. This compound is utilized primarily in pharmaceutical research for the assessment of drug purity and stability. It serves as a critical reference standard in the analytical evaluation of Sertraline formulations, helping to ensure compliance with regulatory quality standards in drug development. -
Drug Impurity
Cinacalcet impurity 4 is a chemical impurity associated with the drug Cinacalcet, which acts as a calcium-sensing receptor agonist. This impurity is relevant for analytical and quality control studies in pharmaceutical development related to Cinacalcet. Its identification and characterization are crucial for ensuring the purity and safety of therapeutic formulations. -
Drug Intermediate
3-Pyrimidin-2-yl-2-pyrimidin-2-ylmethyl-propionic acid is a synthetic intermediate primarily utilized in pharmaceutical synthesis. This compound serves as a crucial building block in the development of various therapeutic agents, facilitating the formation of complex structures for drug discovery. Its applications extend to medicinal chemistry, where it aids in the preparation of bioactive molecules targeting diverse biological pathways. -
Drug Impurity
Quetiapine impurity 10 is a chemical impurity associated with Quetiapine, an atypical antipsychotic. This compound serves as an essential reference standard for the identification and quantification of impurities in pharmaceutical formulations. Its analysis is critical for ensuring the purity and safety of Quetiapine in clinical and research applications. -
Drug Impurity
Methotrexate impurity 5, also known as Methotrexate α-Methyl Ester, is a chemical impurity associated with Methotrexate. This compound may serve as a valuable reference standard for quality control and analytical applications in pharmaceutical research. It aids in the evaluation of the purity and stability of Methotrexate formulations, contributing to the understanding of drug behavior and effectiveness. -
Drug Impurity
Bupropion impurity 18 is a characterized impurity of the antidepressant Bupropion. This compound serves as an important reference standard for analytical methods and quality control in pharmaceutical research. Its presence can influence the pharmacokinetic and pharmacodynamic properties of the parent drug, making it critical for studies evaluating drug safety and efficacy. Bupropion impurity 18 is essential for ensuring the integrity of Bupropion formulations in regulatory assessments. -
Drug Impurity
Acetazolamide impurity 5 is a chemical impurity associated with the drug Acetazolamide, which acts as a carbonic anhydrase inhibitor. This compound is primarily utilized in pharmaceutical research to assess the purity of Acetazolamide formulations and to study its potential effects in drug development. Understanding such impurities is critical for evaluating drug safety, efficacy, and regulatory compliance. -
Drug Impurity
Itraconazole impurity 10, also known as trans-Itraconazole, is a drug impurity associated with the antifungal agent Itraconazole. This compound serves as a valuable reference standard for analytical applications, including pharmacokinetic studies and quality control testing. Its characterization aids in understanding the stability and degradation pathways of Itraconazole in pharmaceutical formulations. Researchers can utilize this impurity to ensure compliance with regulatory standards in drug development. -
Drug Impurity
Testosterone impurity 28 is a defined impurity associated with testosterone. It serves as an important reference standard for the analysis and quality control of testosterone formulations. This impurity can be utilized in various research applications, including pharmacokinetics and toxicology studies, to ensure the integrity and safety of testosterone-related products. -
Drug Impurity
Budesonide impurity 84, also known as Di-Norbudesonide (mixture of diastereomers), serves as a relevant drug impurity in the characterization of Budesonide. This compound is utilized in pharmaceutical research for the investigation of drug stability, efficacy, and safety profiles. Its analysis is crucial for the development and quality control of corticosteroid formulations, ensuring compliance with regulatory standards. -
Drug Impurity
Levofloxacin impurity 10 is a drug impurity associated with the antibiotic levofloxacin. It serves as a key reference standard for analytical testing and quality control in pharmaceutical formulations. This compound plays a critical role in the assessment of drug purity and stability, aiding researchers in ensuring compliance with regulatory standards during drug development processes.
