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| Product | Description | |
|---|---|---|
| 2,3-Dimethyl-p-benzoquinone | 2,3-Dimethyl-p-benzoquinone, a vital organic molecule in industrial applications, serves as a critical chemical precursor in the production process of several drugs and agrochemicals. Aside from its catalytic role in the said domains, this compound also displays paramount significance as a reagent in identifying and evaluating cancer therapeutic agents. Group: Pharmaceutical. CAS No. 526-86-3. Pack Sizes: 500 mg. Product ID: B0001-122179. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| Acetazolamide Impurities | Acetazolamide Impurities hold paramount importance in biomedical applications, facilitating rigorous evaluation of acetazolamide medication's purity, potency, and stability. These substances aid in contaminant identification and quantification, guaranteeing therapeutic safety and efficacy for glaucoma, epilepsy, and altitude-related conditions, thereby refining drug development processes and ensuring regulatory adherence. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ampicillin Impurities | Ampicillin Impurities play a critical role in the pharmaceutical sector, specifically in the quality control process of ampicillin synthesis. These entities aid in identifying potential degradation pathways, thereby ensuring the therapeutic effectiveness and safety of ampicillin, a vital antibiotic combatting diverse bacterial infections, including those of the respiratory and urinary tracts. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Arasertaconazole Impurities | Arasertaconazole Impurities are critical in the quality control and validation processes of antifungal medications, specifically those targeting skin infections like athlete's foot and ringworm. They aid in ensuring the efficacy and safety of arasertaconazole by monitoring and characterizing any by-products or degradation substances during drug synthesis. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Benzethonium Impurities | Benzethonium Impurities, identified in pharmaceutical research, play a critical role in the study of benzethonium chloride's safety and efficacy margins. Understanding these impurities aids in the optimization of antimicrobial formulations, ensuring therapeutic applications while minimizing potential adverse effects. They are integral to quality control investigations in drug development processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Benzopyrene Impurities | Benzopyrene Impurities, widely studied in biomedical research, are critical for investigating carcinogenic processes and drug safety evaluations. These impurities are key factors in understanding the metabolic pathways related to polycyclic aromatic hydrocarbons, which are implicated in various cancers, thereby aiding the development of targeted cancer therapies and screening methodologies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Bilastine Impurities | Bilastine Impurities are crucial for the pharmaceutical industry's quality control processes in antihistamine drug development. These impurities aid in evaluating the safety and efficacy of bilastine, a medication used to alleviate symptoms of allergic rhinitis and urticaria, ensuring the final product's optimal therapeutic performance. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Brivudine Impurities | Brivudine Impurities are instrumental in the pharmaceutical industry for quality control and research processes related to the antiviral drug Brivudine. These impurities aid in understanding the drug's stability, efficacy, and safety profile, particularly in its use against herpes zoster infections. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Bromhexine Impurities | Bromhexine Impurities possess a critical role in the biomedical realm, serving as vital evaluators of bromhexine formulation purity. These entities advance antitussive medication development, ensuring therapeutic safety and effectiveness in addressing respiratory conditions like chronic bronchitis, thereby aiding in airway clearance therapies through meticulous scrutiny and validation processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Carbidopa Impurities | Carbidopa Impurities are critical in evaluating the purity and stability of carbidopa-based medications, primarily used to manage Parkinson's disease symptoms. These impurities aid in refining drug formulation processes, ensuring therapeutic efficacy, and compliance with regulatory standards, thereby contributing significantly to the safe and effective treatment of neurological disorders. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Cefteram Impurities | Cefteram Impurities are critical in the pharmaceutical industry for ensuring the purity and efficacy of the antibiotic cefteram. These impurities are essential for analytical studies and quality control processes, aiding in the development of treatments for bacterial infections, particularly those caused by Gram-positive and Gram-negative bacteria. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Cloperastine Impurities | Cloperastine Impurities are crucial in the pharmaceutical industry for quality control and the development of Cloperastine-based drugs used to treat cough. These impurities aid researchers in refining synthesis processes and ensuring the safety and efficacy of cough suppressants by identifying and characterizing unwanted by-products during drug formulation. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Daunorubicin Impurities | Daunorubicin Impurities, critical reference standards in the biomedical sector, play a pivotal role in the quality control of daunorubicin formulations. These impurities aid in the identification and quantification processes during the production of daunorubicin, a chemotherapy drug used in the treatment of leukemia, ensuring the therapeutic efficacy and safety of the final product. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Degludec Impurities | Degludec Impurities are crucial in the biomedical industry for ensuring the purity and efficacy of insulin degludec formulations. By identifying and quantifying these impurities, researchers can refine pharmaceutical processes, ultimately aiding in the treatment of diabetes mellitus while maintaining drug safety and therapeutic effectiveness. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Demiditraz Impurities | Demiditraz Impurities are critical in the biomedical field for pharmaceutical quality control and drug development processes. These impurities aid in the characterization and refinement of Demiditraz, ensuring therapeutic efficacy and safety in treating parasitic infections, specifically targeting equine parasites, broadening advancements in anti-parasitic agent production. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Dextran | Dextrans are long-chain glucose polysaccharides of various relative molecular mass. Uses: Bacteria growing on a sucrose substrate produce this polysaccharide, which is composed of alpha-d-glucopyranosyl units with different branching and chain lengths; used in soft center confections, as a barley malt substitute, and as a plasma volume expander; mixed ethers and esters can be used in lacquers; used as a formulation and processing aid, stabilizer or thickener, surface finishing agent, and texturizer for foods. Group: Pharmaceutical. CAS No. 9004-54-0. Pack Sizes: 100 g. Product ID: B1999-079228. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Digoxin Impurities | Digoxin Impurities, integral to enhancing digoxin's quality and efficacy, play a crucial role in cardiac glycoside optimization, chiefly for heart failure and atrial fibrillation management. Their meticulous analysis not only ensures drug safety and stability but also elucidates glycoside biosynthetic processes and aids in therapeutic monitoring within cardiovascular treatment paradigms. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Dtpa Impurities | Dtpa Impurities are critical for quality control in the biomedical industry, especially in the purification processes of chelating agents like DTPA, used in MRI contrast and radiopharmaceuticals. Understanding these impurities aids in enhancing the safety and efficacy of imaging agents used in diagnostic applications for conditions like cancer and cardiovascular diseases. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ethane Impurities | Ethane Impurities, often detected in hydrocarbon processing, hold significance in biomedical research for their potential impact on respiratory health and carcinogenesis. Understanding these impurities aids in developing safety standards and evaluation guidelines for chemical exposure, highlighting their role in preventative medicine and public health initiatives. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Fexofenadine Impurities | Fexofenadine Impurities are critical in the quality control and development of the antihistamine drug fexofenadine, used to treat allergy symptoms such as hay fever and chronic urticaria. Studying these impurities aids in ensuring drug purity, efficacy, and safety during pharmaceutical manufacturing processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Fludrocortisol Impurities | Fludrocortisol Impurities are critical in the biomedical industry for the qualitative analysis of fludrocortisone acetate, a crucial medication used in treating conditions like Addison's disease and congenital adrenal hyperplasia. These impurities aid in ensuring the drug's purity and effectiveness through rigorous quality control processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Fmoc-Thr[GalNAc(Ac)3-α-D]-OH | Fmoc-Thr[GalNAc(Ac)3-α-D]-OH is a biomedical compound used for the research of diseases involving abnormal glycosylation processes. It functions as a glycosylation inhibitor, targeting enzymes responsible for glycan modification. This product aids in the study and understanding of glycosylation-related disorders. Group: Pharmaceutical. CAS No. 116783-35-8. Pack Sizes: 25 mg. Product ID: BAT-008014. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Gestonorone Impurities | Gestonorone Impurities are vital entities within the biomedical sector, crucial for rigorous quality control and validation processes of gestonorone-based hormonal therapies. These impurities aid in refining and augmenting treatments for hormone-related disorders, such as endometriosis and menopausal conditions, ensuring both therapeutic efficacy and safety. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Histidine Impurities | Histidine Impurities are critical in the biomedical field for the analysis and characterization of pharmaceuticals, especially in quality control processes. They aid in identifying degradation products in histidine-based formulations, ensuring drug efficacy and safety. Additionally, understanding these impurities supports research into amino acid metabolism disorders. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Hydroxychloroquine Impurities | Hydroxychloroquine Impurities are critical in analytical and quality control processes for ensuring the safety and efficacy of hydroxychloroquine used in treating malaria, rheumatoid arthritis, and lupus erythematosus. These impurities aid in refining hydroxychloroquine formulations and improving therapeutic performance. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Idelalisib Impurities | Idelalisib Impurities are essential for pharmaceutical research and development, offering insights into the stability and efficacy of the drug Idelalisib, used to treat chronic lymphocytic leukemia and follicular lymphoma. Analysis of these impurities aids in improving Idelalisib formulations and ensuring quality control in drug manufacturing processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Insulin Impurities | Insulin Impurities are by-products in insulin production, utilized in the biomedical field for quality control and safety assessment of insulin formulations. They play a crucial role in ensuring the therapeutic efficacy and minimizing adverse reactions in diabetes treatment. Studying these impurities aids in optimizing insulin manufacturing processes and improving diabetes management strategies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Labetalol Impurities | Labetalol Impurities are critical in the biomedical industry for ensuring the purity and efficacy of labetalol, a medication used to manage hypertension and angina. The identification and quantification of these impurities aid in drug formulation, enhancing therapeutic outcomes and ensuring patient safety through rigorous quality control processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Lanreotide Impurities | Lanreotide Impurities are instrumental in the quality control processes of lanreotide, aiding in the management of acromegaly and neuroendocrine tumor symptoms. These components are crucial for evaluating the drug's purity, stability, and safety parameters, ensuring adherence to rigorous pharmaceutical standards for therapeutic effectiveness. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Lenalidomide Impurities | Lenalidomide Impurities are crucial in the pharmaceutical analysis and quality control of lenalidomide, a drug primarily used for treating multiple myeloma and myelodysplastic syndromes. Understanding these impurities aids in refining the production process, ensuring the efficacy and safety of lenalidomide for clinical applications in oncology. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Leq-506 Impurities | Leq-506 Impurities are critical in the biomedical industry for understanding the chemical profile and stability of Leq-506, a promising investigational drug for chronic myeloid leukemia (CML) treatment. These impurities aid in refining synthesis processes and ensuring drug efficacy and safety, enhancing therapeutic applications for leukemia patients. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Levocetirizine Impurities | Levocetirizine Impurities, byproducts in the synthesis of levocetirizine, play a crucial role in assessing the drug's quality and safety for treating allergic rhinitis and chronic urticaria. Their study aids in refining purification processes, ensuring therapeutic efficacy and compliance with regulatory standards in allergy management. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Metalaxyl Impurities | Metalaxyl Impurities hold notable importance in pharmaceutical research, primarily in the context of enhancing fungicide formulations. These impurities aid scientists in deciphering the metabolic pathways and degradation processes of Metalaxyl, an essential agricultural fungicide, thereby facilitating the development of safer, more effective strategies for combating oomycete-induced crop diseases. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Methimazole impurities | Methimazole impurities are by-products found in preparations of methimazole, a crucial drug for managing hyperthyroidism. Understanding these impurities aids in ensuring drug safety and efficacy. Additionally, studying these impurities can contribute to refining synthesis processes and improving therapeutic outcomes for thyroid-related disorders. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Moexiprilat Impurities | Moexiprilat Impurities, crucial for quality control in pharmaceuticals, are studied to ensure purity in the production of moexipril, an antihypertensive medication. Understanding these impurities aids in refining the synthesis processes, significantly enhancing the safety and efficacy of drugs used to manage hypertension and cardiovascular conditions. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Mometasone Furoate Impurities | Mometasone Furoate Impurities are utilized in the pharmaceutical industry to ensure the potency and safety of mometasone-based drugs. These impurities play a crucial role in the quality control process, aiding in the treatment of inflammatory dermatological conditions, such as eczema and psoriasis, by ensuring drug efficacy and regulatory compliance. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Naftopidil Impurities | Naftopidil Impurities are essential constituents in pharmaceutical exploration, specifically targeting benign prostatic hyperplasia and hypertension treatments. These impurities unveil critical insights into naftopidil's pharmacokinetics and safety frameworks, aiding in therapeutic optimization and adverse effect reduction, thereby augmenting the efficacy of drug development processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nefopam Impurities | Nefopam Impurities, crucial in pharmaceutical quality control, aid in evaluating the purity and stability of nefopam hydrochloride, an analgesic used to treat moderate to severe pain. Understanding these impurities ensures drug safety and efficacy, providing assurance in the production process and furthering drug development for pain management therapies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nelfinavir Impurities | Nelfinavir Impurities are crucial analytical tools in the biomedical industry for ensuring the quality and safety of Nelfinavir, an antiretroviral protease inhibitor used in treating HIV-1 infections. These impurities aid in developing purification processes and conducting rigorous stability studies, thereby enhancing therapeutic efficacy and patient safety. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| NITRIC ACID 67% | A inorganic compound with the formula HNO3. It is a highly corrosive mineral acid. The compound is colourless, but older samples tend to be yellow cast due to decomposition into oxides of nitrogen. Most commercially available nitric acid has a concentration of 68% in water. When the solution contains more than 86% HNO3, it is referred to as fuming nitric acid. Depending on the amount of nitrogen dioxide present, fuming nitric acid is further characterized as red fuming nitric acid at concentrations above 86%, or white fuming nitric acid at concentrations above 95%. Uses: Intermediate for chemical syntheses.Intermediate in manufacture of inorganic and organicchemicals incl. fertilizers.Formulation of mixtures (fertilizer, metal surfacetreatment product, cleaning product, detergent andmaintenance product).Processing aid in industry, including laboratoryapplications, such as pH regulator, neutralisationagent, oxidising agent.Reactive agent in inorganic and organic synthesis.Regeneration of ion exchange resins.pH control.Laboratory agent.Surface treatment product. In cleaning products. CAS No. 7697-37-2. |  |
| NITRIC ACID 99% (CONCENTRATED) | A inorganic compound with the formula HNO3. It is a highly corrosive mineral acid. The compound is colourless, but older samples tend to be yellow cast due to decomposition into oxides of nitrogen. Most commercially available nitric acid has a concentration of 68% in water. When the solution contains more than 86% HNO3, it is referred to as fuming nitric acid. Depending on the amount of nitrogen dioxide present, fuming nitric acid is further characterized as red fuming nitric acid at concentrations above 86%, or white fuming nitric acid at concentrations above 95%. Uses: Intermediate for chemical syntheses.Intermediate in manufacture of inorganic and organic chemicals incl. fertilizers.Formulation of mixtures (fertilizer, metal surface treatment product, cleaning product, detergentand maintenance product).Processing aid in industry, including laboratory applications, such as pH regulator, neutralisationagent, oxidising agent.Reactive agent in inorganic and organic synthesis.Regeneration of ion exchange resins.pH control.Laboratory agent.Surface treatment product.In cleaning products. CAS No. 007-004-00-1. | |
| Pelargonidin Impurities | Pelargonidin Impurities are utilized in the biomedical industry to study and analyze anthocyanin molecules. These impurities aid in the investigation of antioxidative and anti-inflammatory properties, important for developing therapeutic strategies against cardiovascular diseases and cancer. They also serve as reference standards in analytical testing and quality control processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Phenethylamine Impurities | Phenethylamine Impurities play a crucial role in drug development processes, particularly in ensuring the purity and efficacy of psychoactive medications. They are essential in the study of diseases related to neurological functions, showing potential in aiding the development of treatments for conditions like depression, ADHD, and neurodegenerative disorders. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| p-Nitrophenyl 2-Acetamido-2-deoxy-α-D-galactopyranoside | p-Nitrophenyl 2-Acetamido-2-deoxy-α-D-galactopyranoside is an essential compound in biomedicine. It is commonly utilized in the production of synthetic substrates for studying glycosidase enzymes. This compound is valuable in research concerning carbohydrate chemistry, specifically in the investigation of enzymes involved in breaking down glycosylation processes. It plays a crucial role in medicinal chemistry by aiding in the development of drugs targeting certain diseases related to carbohydrate processing and glycosylation disorders. Group: Pharmaceutical. CAS No. 23646-68-6. Pack Sizes: 25 mg. Product ID: B1370-059264. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| POLY ALUMINIUM CHLORIDE | As a highly effective coagulant and flocculant, poly aluminium chloride (PAC) is largely used in the water treatment industry and works across several different applications to include drinking water treatment, process water treatment, effluent treatment, and wastewater treatment. Poly aluminium Chloride is also used in swimming pool water treatment as a clarification and filtration aid. Uses: Laboratory chemicals, manufacture of substances. CAS No. 1327-41-9. | |
| Pravastatin Impurities | Pravastatin Impurities hold a crucial position within the biomedical sector, facilitating the analytical dissection and quality assurance of pravastatin—a pivotal cholesterol-lowering agent combating cardiovascular issues. These impurities aid in the pharmaceutical development and validation processes, thereby guaranteeing the therapeutic efficacy and safety of lipid-lowering treatments. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Prazosin Impurities | Prazosin Impurities are crucial in the biomedical industry for drug development and quality control of prazosin, an antihypertensive medication. Studying these impurities aids in understanding drug stability, refining purification processes, and ensuring safety and efficacy in treating hypertension-related disorders, including prostatic hyperplasia and congestive heart failure. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Quinagolide Impurities | Quinagolide Impurities play a profound role in the biomedical field by aiding in analytical processes crucial for the development and quality control of quinagolide, a dopamine agonist. This analysis supports research and treatment of conditions like hyperprolactinemia, thereby enhancing therapeutic precision and efficacy in clinical applications. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sucralose Impurities | Sucralose impurities play a crucial role in the biomedical industry's quality control processes for sucralose products. Monitoring these impurities ensures the safety and efficacy of sucralose, widely used in pharmaceuticals and diabetic treatment formulations, by maintaining stringent standards and aiding in the identification of any potential toxicological concerns. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Talinolol Impurities | Talinolol Impurities, trace compounds present in pharmaceutical formulations, are crucial in quality control and drug development processes related to cardiology. They aid in the analysis and refinement of talinolol, a beta-blocker used in the management of hypertension and heart disease, ensuring the drug's safety and efficacy in clinical applications. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Teclozan Impurities | Teclozan Impurities refer to trace components arising during the synthesis of the antiprotozoal drug Teclozan. Their identification and analysis are crucial in quality control processes for ensuring drug safety and efficacy, particularly in treating intestinal amebiasis. Additionally, understanding these impurities can aid in refining synthesis protocols and enhancing therapeutic outcomes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Telotristat Impurities | Telotristat Impurities are crucial in the pharmaceutical industry for quality control and development of telotristat ethyl-based medications. Identifying and analyzing these impurities ensure the safety and efficacy of treatments primarily used for managing carcinoid syndrome diarrhea, associated with neuroendocrine tumors. They aid in refining purification processes for optimal therapeutic outcomes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Terlipressin Impurities | Terlipressin Impurities, critical in quality control processes of terlipressin synthesis, aid in ensuring the efficacy and safety of this vasopressor agent. Primarily used in managing esophageal variceal hemorrhage in cirrhotic patients, it plays a vital role in understanding and minimizing adverse reactions associated with terlipressin treatment. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Vilanterol Impurities | Vilanterol Impurities are pivotal in the biomedical industry for analytical and quality control processes in drug development. These impurities aid in understanding the pharmacokinetics and stability of Vilanterol, a long-acting beta agonist used in treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Vitamin E Impurities | Vitamin E Impurities possess critical significance in the analytical realm, underpinning the validation processes of Vitamin E formulations to secure purity and therapeutic effectiveness. Integral to quality assurance, these impurities aid in evaluating oxidative stress-related conditions and cardiovascular afflictions, ultimately steering the development of safer, efficacious pharmaceutical innovations. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Walsuronoid B Impurities | Walsuronoid B Impurities are significant in the biomedical industry for understanding and ensuring the purity and efficacy of Walsuronoid B, a compound with potential therapeutic applications. Their analysis aids in drug development processes, particularly for treatments targeting inflammatory diseases and certain cancers. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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