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| Product | Description | |
|---|---|---|
| BENCH MAT | BENCH MAT, Suppliers of UK laboratory chemicals wanted |  |
| Acepromazine Impurities | Acepromazine Impurities function as essential analytical benchmarks within the biomedical sector, ensuring the quality assurance and safety protocols of acepromazine formulations, predominantly employed as veterinary tranquilizers. These impurities facilitate precise identification and quantification, underpinning robust drug quality control and paramount regulatory adherence. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| Adamantane Impurities | Adamantane Impurities are pivotal in the pharmaceutical industry for ensuring the purity and effectiveness of antiviral drugs, particularly those targeting influenza viruses, like amantadine and rimantadine. By defining contamination benchmarks, these impurities help ascertain drug safety and efficacy, facilitating research innovation in antiviral treatment methodologies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Aflatoxin Impurities | Aflatoxin Impurities hold a crucial place in biomedical research as they elucidate foodborne contamination and detoxification paradigms. Examination of these impurities aids in setting safety benchmarks and devising targeted interventions for aflatoxin-induced hepatic afflictions like hepatocellular carcinoma, thus refining toxicological prevention and therapeutic methodologies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Aliskiren Impurities | Aliskiren Impurities act as essential analytical benchmarks, vital for the rigorous quality control assessment in the synthesis of Aliskiren, a key renin inhibitor used for hypertension treatment. By assuring purity and stability, they crucially optimize therapeutic precision and drive advancements in the development of safer cardiovascular interventions. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Amodiaquine Impurities | Amodiaquine Impurities assume vital roles as analytical benchmarks in the pharmaceutical landscape, predominantly aiding in the stringent quality control and validation protocols of amodiaquine formulations. Considered crucial antimalarial agents against Plasmodium falciparum and Plasmodium vivax, their meticulous impurity scrutiny ensures therapeutic efficacy alongside patient safety. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Anagliptin Impurities | Anagliptin Impurities, crucial in the biomedical sector, facilitate the analysis of anagliptin's purity and stability. These impurities serve as benchmarks in quality control for developing diabetes medications, ensuring effective glycemic regulation. Such analytical advancements aid in refining therapeutic strategies for type 2 diabetes management. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Arimoclomol Impurities | Arimoclomol Impurities, essential in drug formulation and quality assurance, play a crucial role in neurodegenerative research. They are instrumental in ascertaining the purity and safety of Arimoclomol, primarily used for the treatment of amyotrophic lateral sclerosis (ALS) and Niemann-Pick disease type C, thus elevating therapeutic benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Atosiban Impurities | Atosiban Impurities, fundamental to the biomedical realm, act as critical benchmarks for evaluating and synthesizing Atosiban, a drug used in managing preterm labor. By confirming purity and potency, these impurities significantly enhance therapeutic safety against early uterine contractions, thereby ensuring maternal-fetal welfare. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Buspirone Impurities | Buspirone Impurities, fundamental analytical benchmarks in the biomedical sector, are integral for the assurance of quality and reliability in buspirone synthesis. Their critical role encompasses evaluating buspirone's safety and efficacy, primarily utilized in anxiety disorder management, thus ensuring its purity and consistent therapeutic reliability. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Carbendazim Impurities | Carbendazim Impurities, meticulously examined for their biomedical implications, play a crucial role in pharmacological research. Serving as essential benchmarks, they influence drug formulation and safety evaluations, particularly in antifungal and antineoplastic contexts, thus ensuring therapeutic efficacy and safety in managing systemic mycoses and specified malignancies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Carprofen Impurities | Carprofen Impurities, quintessential in analytical research, underpin quality assessment and structural analysis of Carprofen, a nonsteroidal anti-inflammatory agent. Their examination is imperative for maintaining stringent safety, efficacy, and purity benchmarks, crucial for mitigating osteoarthritic pain and inflammation, particularly within veterinary medicine. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Cevimeline Impurities | Cevimeline Impurities, indispensable in pharmaceutical refinement, serve a critical function in the formulation of cevimeline for Sjögren's syndrome's xerostomia relief. Their presence is crucial for delineating safety frameworks, enhancing the understanding and elevation of cevimeline's therapeutic efficacy and quality benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Clofentezine Impurities | Clofentezine Impurities function as vital analytical benchmarks in the precise study and quality verification of clofentezine, an acaricide of specificity. Meticulous analysis of these impurities guarantees the pesticide's safety and efficacy, influencing environmental assessment and biomedical scrutiny related to pesticide exposure's health implications. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Danofloxacin Impurities | Danofloxacin Impurities function as essential analytical constituents, upholding the purity benchmarks of danofloxacin, a fluoroquinolone antibiotic utilized against animal bacterial afflictions. These impurities aid in discerning by-products and degradation derivatives, a crucial procedure guaranteeing the safety and efficacy of veterinary pharmaceuticals targeting respiratory and enteric maladies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Desogestrel Impurities | Desogestrel Impurities hold paramount importance in the realm of pharmaceutical quality assurance, crucial for the safety evaluation of contraceptive formulations. These impurities facilitate efficacy and stability in desogestrel-based contraceptives, essential for hormonal birth control, by ensuring adherence to regulatory benchmarks and enhancing drug formulation methodologies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Diflunisal Impurities | Diflunisal Impurities, serving as essential analytical benchmarks in the biomedical sphere, underpin the assurance of diflunisal's purity and therapeutic effectiveness, this non-steroidal anti-inflammatory agent instrumental in pain alleviation and arthritis management. They facilitate rigorous quality control protocols during the pharmaceutical production process, ensuring the highest standards in drug manufacturing. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Diosmin Impurities | Diosmin Impurities hold a vital position within pharmaceutical quality control, especially concerning chronic venous insufficiency and hemorrhoid therapies. These compounds are essential for assessing the purity and efficacy of diosmin formulations, acting as sentinels against adulterants and guaranteeing adherence to therapeutic benchmarks, thereby ensuring medicinal integrity. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| DLinDMA | DLinDMA, an ionizable cationic lipid, is a key lipid component of stable nucleic acid lipid particles (SNALPs) as a benchmark. Group: Pharmaceutical. CAS No. 871258-12-7. Pack Sizes: 100 mg. Product ID: B4059-051365. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Donepezil Impurities | Donepezil Impurities are integral to the biomedical field, serving as analytical benchmarks to ascertain the quality and efficacy of donepezil, a treatment predominantly for Alzheimers. These impurities are vital in the pharmacological analysis and refinement of donepezil formulations, contributing to the advancement of therapeutic efficacy in neurodegenerative conditions. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Dutasteride Impurities | Dutasteride Impurities are integral in ensuring the pharmaceutical fidelity and safety of Dutasteride, vital in managing benign prostatic hyperplasia. Through rigorous scrutiny of impurities, therapeutic efficacy is maintained and adverse effects mitigated, proving crucial in pharmaceutical formulation and compliance, and ultimately elevating biomedical industry benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Estradiol Impurities | Estradiol Impurities, integral to the biomedical sector, are essential benchmarks ensuring the integrity of estradiol formulations. They underlie stringent quality control processes in hormone therapy development, addressing menopausal and osteoporotic conditions while safeguarding therapeutic efficacy and safety through meticulous standardization and verification practices. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Faropenem Impurities | Faropenem Impurities occupy a critical niche in the biomedical realm, acting as benchmarks to assess the purity and safety of Faropenem, a broad-spectrum antibiotic. The meticulous management and control of these impurities are essential to ensure the therapeutic efficacy and safety of the drug, particularly in combating respiratory and urinary infections. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Felypressin Impurities | Felypressin impurities, serving as critical analytical benchmarks, facilitate the evaluation of purity and stability of this vasoconstrictor, often coupled with lidocaine in dental anesthetics. Scrutiny of these impurities proves essential for verifying pharmacological efficacy and safety, mitigating adverse responses in clinical settings where felypressin is employed. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Flomoxef Impurities | Flomoxef Impurities stand as essential reference benchmarks in the pharmaceutical realm, playing a crucial role in the analytical evaluation and quality assurance of Flomoxef, a cephalosporin antibiotic. Examining these impurities is pivotal for maintaining Flomoxef's therapeutic efficacy against bacterial afflictions like respiratory and urinary tract infections, thereby enhancing antimicrobial treatment strategies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Gadoteridol Impurities | Gadoteridol Impurities hold paramount importance in scrutinizing the purity and safety benchmarks of gadoteridol-based contrast media utilized in MRI. Their comprehensive analysis elevates diagnostic accuracy, diminishing adverse risk, thereby fundamentally contributing to advances in neuroimaging and vascular diagnostics. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Iminostilbene Impurities | Iminostilbene Impurities hold a critical role in the biomedical sector, serving as analytical benchmarks for purity assessment in anticonvulsant pharmaceuticals, notably carbamazepine. These impurities facilitate evaluations of drug safety, therapeutic efficacy, and stringent quality control, which are essential components in the production of epilepsy and trigeminal neuralgia treatments. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Kaempferol Impurities | Kaempferol Impurities are instrumental in the biomedical sector, functioning as reference benchmarks for the scrutiny and quality assurance of kaempferol-related pharmaceutical products. These impurities facilitate the assessment of kaempferol's purity, which is under exploration for therapeutic potential in addressing diverse inflammatory ailments and oncological conditions. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Lacosamide Impurities | Lacosamide Impurities, serving as essential analytical benchmarks, are foundational in the pharmaceutical realm to ensure the purity and efficacy of lacosamide, a vital therapeutic agent for partial-onset epileptic seizures. These impurities enable stringent quality assurance, enhancing the safety and clinical reliability of the drug while optimizing performance metrics. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Letrozole Impurities | Letrozole Impurities are crucial in the biomedical field for assessing the purity and stability of the drug Letrozole, used in the treatment of hormone receptor-positive breast cancer. These impurities aid in research to improve drug formulations and ensure their therapeutic efficacy, serving as benchmarks for quality control in pharmaceutical development. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Leucoson Impurities | Leucoson Impurities, indispensable analytical benchmarks in the biomedical sector, play an essential role in the detection and quantification of contaminants throughout Leucoson production. This pharmaceutical is crucial for dermatological disorder management. These impurities ensure drug safety and efficacy, underpinning rigorous quality control and compliance with regulatory standards. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Levomefolate Impurities | Levomefolate Impurities function as crucial benchmarks in pharmaceutical realms, underpinning the advancement and quality assurance of folate-centric medications. They are instrumental in validating the efficacy and safety profiles of therapies addressing major depressive disorder and cardiovascular conditions, offering profound insights into drug stability and bioavailability parameters. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Metolazone Impurities | Metolazone Impurities hold paramount significance in the pharmaceutical domain, meticulously scrutinizing and verifying the purity of metolazonea diuretic combating hypertension and edema linked to cardiac and renal conditions. This rigorous analysis not only advances drug safety and efficacy but also ensures adherence to stringent regulatory benchmarks, thus bolstering therapeutic efficacy. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Metoprolol Impurities | Metoprolol Impurities hold significant importance within the biomedical sector, serving as reference benchmarks essential for the rigorous quality control and analytical scrutiny of the beta-blocker Metoprolol. Employed in managing hypertension, angina, and heart failure, these impurities are vital to affirming the therapeutic formulations' efficacy and safety in clinical applications. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Miconazole Impurities | Miconazole Impurities, crucial components within the pharmaceutical realm, function as analytical benchmarks in antifungal drug quality control. They enable precise identification and quantification of active ingredients, thereby safeguarding the therapeutic efficacy and safety of treatments for fungal ailments, including athlete's foot, jock itch, and candidiasis, thus advancing clinical pharmacology. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Miglitol Impurities | Miglitol Impurities, integral to the biomedical sector, function as reference benchmarks for quality control in Miglitol production. Serving as a critical antihyperglycemic agent in type 2 diabetes management, the assurance of its purity and efficacy is paramount, underscoring the therapeutic effectiveness essential for such medical interventions. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Molnupiravir Impurities | Molnupiravir Impurities, indispensable in the realm of biomedical scrutiny, function as critical benchmarks for ascertaining the synthesis fidelity of Molnupiravir. These impurities are central to maintaining the drugs structural integrity and antiviral potency against COVID-19, restraining viral expansion while upholding stringent regulatory and pharmacological standards. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nebramine Impurities | Nebramine Impurities are critical reference standards in the biomedical industry, utilized for quality control and validation in the synthesis of antimalarial and antiparasitic drugs. These impurities assist in ensuring the purity and efficacy of pharmaceutical formulations by providing benchmarks for analytical assessment during drug development processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nifuroxazide Impurities | Nifuroxazide Impurities, quintessential in the biomedical sector, underpin quality assurance and in-depth scrutiny of nifuroxazide-based formulations. Predominantly utilized as a reference benchmark in gastrointestinal infection research, they ensure the purity and therapeutic effectiveness of the principal drug in combating bacterial diarrhea, thus fortifying clinical outcomes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Nisoldipine Impurities | Nisoldipine Impurities embody essential analytical benchmarks within pharmaceutical development, crucial for the meticulous quality control of Nisoldipine, a calcium channel antagonist addressing hypertension and angina. Their analytical utility lies in assuring Nisoldipines therapeutic efficacy and safety by rigorously assessing purity metrics throughout manufacturing paradigms. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Oxeladin Citrate Impurities | Oxeladin Citrate Impurities, esteemed reference benchmarks within the pharmaceutical sector, play an instrumental role in affirming the purity and therapeutic potency of the antitussive agent Oxeladin Citrate. Employed in alleviating persistent coughs, these impurities are vital for stringent quality control throughout drug formulation and production stages. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Oxiracetam Impurities | Oxiracetam Impurities are indispensable in the rigorous realm of pharmaceutical quality assurance for the nootropic agent oxiracetam. Through meticulous analysis, these impurities ensure the drugs purity and potency, essential for cognitive disorder treatments, including Alzheimer's. Their detection is vital for adhering to stringent regulatory safety benchmarks, safeguarding therapeutic efficacy. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Patupilone Impurities | Patupilone Impurities, essential reference benchmarks in the realm of quality control and analytical cancer research, illuminate the metabolic intricacies of Patupilone, an investigative anticancer compound. These impurities are instrumental in validating efficacy and safety, facilitating the optimization of its formulation and unveiling its pharmacokinetic characteristics. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Penehyclidine Impurities | Penehyclidine Impurities, byproducts arising from penehyclidine synthesis, undergo meticulous scrutiny within pharmaceutical realms. Their examination is vital for ensuring drug safety and therapeutic effectiveness, particularly significant in treating respiratory and neurological maladies. These analyses support stringent quality control and adhere to regulatory benchmarks in advanced drug formulation. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Pilocarpine Impurities | Pilocarpine Impurities hold a critical position in pharmaceutical research, serving as essential benchmarks for quality control in pilocarpine medications, predominantly targeting glaucoma and xerostomia conditions. These impurities facilitate rigorous analysis, ensuring both efficacy and safety, thus refining the processes of drug formulation and production for optimal therapeutic outcomes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Pralidoxime Chloride Impurities | Pralidoxime Chloride Impurities function as essential analytical benchmarks integral to assessing pralidoxime chloride's purity and therapeutic potency. Within nerve agent and organophosphate pesticide toxicity interventions, these impurities ensure rigorous safety and efficacy through precise profiling, fundamentally supporting stringent pharmaceutic quality assurance protocols. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Propiconazole Impurities | Propiconazole Impurities constitute essential reference benchmarks in pharmaceutical exploration, particularly in the synthesis and evaluation of antifungal compounds. They illuminate metabolic pathways and safety profiles of the drug, notably in addressing fungal afflictions like athlete's foot and ringworm, thereby enhancing therapeutic efficacy and minimizing adverse impacts. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Racecadotril Impurities | Racecadotril Impurities, emerging as consequential by-products in antidiarrheal production, embody a critical facet within rigorous quality control paradigms. Their meticulous monitoring is pivotal for ensuring the safety and therapeutic efficacy of racecadotril in managing acute diarrhea, thereby enhancing pharmaceutical benchmarks and assuring regulatory compliance. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Rilmenidine Impurities | Rilmenidine Impurities function as essential analytical benchmarks within the realms of quality assurance and stability evaluation for the antihypertensive agent, rilmenidine. They are instrumental in verifying the therapeutic reliability and safety of rilmenidine, enabling the detection and quantification of degradation by-products and process-related contaminants in drug formulations. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ronidazole Impurities | Ronidazole Impurities are indispensable analytical benchmarks within the biomedical sector, pivotal for ensuring Ronidazole's quality, an antimicrobial agent treating avian infections such as trichomoniasis. These impurities' quantification is integral to verifying the safety and therapeutic efficacy of Ronidazole formulations, thereby safeguarding veterinary health standards. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ruxolitinib Impurities | Ruxolitinib Impurities represent crucial reference substances within the biomedical arena, instrumental in the fabrication and innovation of therapeutic agents for myelofibrosis and polycythemia vera. These impurities are integral to quality assurance and analytical scrutiny, fortifying the efficacy and safety benchmarks of ruxolitinib, a potent JAK inhibitory compound. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Semaglutide Impurities | Semaglutide Impurities are crucial analytical benchmarks in the biomedical field, predominantly utilized in quality control for semaglutide manufacturing. They help to ensure the purity of the semaglutide used in treating type 2 diabetes and obesity, thereby safeguarding efficacy and safety in pharmaceutical applications. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sitagliptin Impurities | Sitagliptin Impurities function as essential constituents in the biomedical sector, facilitating the meticulous evaluation of Sitagliptin's purity and safety. Integral to quality assurance during drug development, they ascertain therapeutic efficacy for type 2 diabetes patients by verifying the lack of undesirable byproducts, upholding superior pharmaceutical benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sofosbuvir Impurities | Sofosbuvir Impurities hold pivotal importance within the biomedical realm, facilitating the meticulous examination of Sofosbuvir's synthesis and quality. Critical in addressing hepatitis C treatment, these impurities serve as essential benchmarks, ensuring the drugs purity, efficacy, and safety, thus underpinning rigorous pharmaceutical analysis and development. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Spironolactone Impurities | Spironolactone Impurities hold a crucial position in the biomedical sector, underpinning the stringent quality assurance and safety assessment of spironolactone. This pharmaceutical agent, utilized for hypertension, heart failure, and hyperaldosteronism management, achieves its therapeutic efficacy and safety through meticulous impurity analysis, thereby upholding superior pharmaceutical benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sugammadex Impurities | Sugammadex Impurities, integral to the biomedical realm, serve as reference benchmarks in the meticulous quality control of Sugammadex. This drug, pivotal in reversing neuromuscular blockade amid anesthesia, demands precise impurity identification and quantification to uphold medicinal safety and efficacy during surgical interventions, thereby enhancing procedural outcomes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sulbactam Impurities | Sulbactam Impurities, as critical analytical benchmarks, are integral to the biomedical sector for validating sulbactam formulation integrity. These impurities facilitate the detection of degradation byproducts in sulbactam, a beta-lactamase antagonist essential for combating bacterial infections and amplifying the efficacy of beta-lactam antibiotic therapies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sulbutiamine Impurities | Sulbutiamine Impurities, integral to pharmaceutical exploration, are essential for verifying drug safety and efficacy. These compounds facilitate the detection of degradation byproducts in stability evaluations, particularly pertinent to asthenia and central nervous system therapies. Scrutiny of such impurities is vital in upholding rigorous quality benchmarks in medication formulation. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sulfadiazine Impurities | Sulfadiazine Impurities act as essential reference benchmarks within pharmaceutical quality assurance. These impurities are central to refining and validating sulfadiazine's sulfonamide antibiotic compositions, vital for addressing urinary tract infections, toxoplasmosis, and various bacterial pathogens, thereby reinforcing pharmacotherapeutic efficacy and safety standards. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Taltirelin Impurities | Taltirelin Impurities, indispensable analytical benchmarks, critically assess pharmaceutical integrity and performance within biomedical realms. Through facilitating Taltirelin's quality assurancethis thyrotropin-releasing hormone analogue for spinocerebellar degenerationimpurities ensure uniform therapeutic results, thereby enhancing the medications safety and efficacy, and solidifying rigorous standards in drug evaluation. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Terazosin Impurities | Terazosin Impurities, vital components in pharmaceutical scrutiny, meticulously evaluate the compositional integrity and therapeutic effectiveness of Terazosin, employed against hypertension and benign prostatic hyperplasia. Rigorous analysis of these impurities secures Terazosin's safety and therapeutic fidelity, thereby refining drug production quality and elevating pharmacological benchmarks. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tiopronin Impurities | Tiopronin Impurities, serving as indispensable reference benchmarks, are crucial within pharmaceutical research. They underpin the assurance of Tiopronin formulation quality and safety by elucidating drug stability, degradation pathways, and toxicity profiles. These insights are vital for therapeutic strategies in cystinuria, simultaneously advancing diverse drug-development initiatives. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tizanidine Impurities | Tizanidine Impurities hold paramount importance as analytical benchmarks within the pharmaceutical realm, facilitating rigorous quality control and stability evaluations of Tizanidine, a muscle relaxant prescribed for spasticity in multiple sclerosis, spinal trauma, and cerebral palsy. These impurities underscore the imperative of drug safety and efficacy during both formulation and production phases. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Treprostinil Impurities | Treprostinil Impurities hold paramount importance in the realm of quality control and pharmacological exploration concerning treprostinil, a therapeutic agent targeting pulmonary arterial hypertension. These impurities furnish essential reference benchmarks, aiding in the precise identification and quantification of impurities, thereby fortifying the efficacy and safety of treprostinil formulations during drug manufacturing intricacies. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Trimeprazine Impurities | Trimeprazine Impurities function as vital analytical benchmarks within the biomedical domain, crucially facilitating the advancement and quality assurance of antihistamine pharmaceuticals. Through elucidating drug purity, these impurities enhance the therapeutic efficacy and safety of trimeprazine formulations, specifically in ameliorating conditions such as allergies and pruritic skin disorders. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Vilazodone Impurities | Vilazodone Impurities, serving as critical analytical benchmarks in the pharmaceutical sector, underpin quality control and formulation processes for vilazodone, a therapeutic agent for major depressive disorder. These impurities elucidate the drug's stability, efficacy, and safety, ensuring compliance with stringent regulatory standards and enhancing therapeutic reliability. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Vildagliptin Impurities | Vildagliptin Impurities are critical in the pharmaceutical sector for assessing the purity of Vildagliptin, a medication widely used to manage type 2 diabetes by inhibiting dipeptidyl peptidase-4 (DPP-4). These impurities serve as benchmarks to ensure drug safety and efficacy during formulation and quality control processes. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Zalcitabine Impurities | Zalcitabine Impurities are critical in the quality control analysis of antiretroviral medications used notably in HIV treatment. These impurities provide benchmarks for pharmacological safety, ensuring therapeutic efficacy and patient safety, by allowing accurate determination of degradation products and synthesis by-products in zalcitabine formulations. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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