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Dotinurad Related Impurities
As a novel urate-lowering drug, impurity control is a critical step in ensuring its pharmaceutical safety. Dotinurad-related impurities primarily stem from synthesis process byproducts and d...
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Vitamin B6 (Pyridoxine) Impurity
Vitamin B6 is not resistant to high temperatures and is easily destroyed under light and alkaline conditions, with more degradation impurities. Different impurities may also be generated during the...
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Loxoprofen Impurity
Notably, brominated intermediates from synthesis may carry potential toxicity, while impurities such as ring-opened degradants and glycerol-esterified byproducts can compromise drug e...
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Vitamin K impurity
To address pain points in procurement, SZEB offer a full life-cycle management program: We supplies a complete range of Vitamin K impurities, including:Vitamin K1 Impurity Series...
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Finerenone impurity
SZEB supplies a comprehensive portfolio of Finerenone impurity reference standards, including stereoisomers such as: (S)-Finerenone、(R)-Finerenone、Finerenone racemate,Below i...
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Lipoic Acid Impurity
SZEB supplies a full range of lipoic acid impurities in stock, including the main process impurities in the preparation of lipoic acid, such as: cyclization by-product impurity A , CAS: 12042...
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Vilanterol Impurity——in stock
SZEB provides a full suite of vilanterol impurities to accelerate generic drug bioequivalence studies and originator process optimization. Our offerings include: N-Nitroso vilanterol ...
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Eltrombopag Impurity
SZEB specializes in supplying a comprehensive range of eltrombopag impurities, including:EP-specified impurities、Eltrombopag olamine、Dimer-related impurities These referenc...
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Azithromycin Impurities——in stock
Azithromycin A 11,12-cyclic borate 3’-N-Demethyl-3’-N-(phenylsulfonyl) azithromycin 3-Hydroxy azithromycin acid For detailed impurity profiles and inquiries, visit http://www.ex-biotech.c...
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Brexpiprazole: A Third-Generation Antipsychotic...
在其实际生产工艺中,会涉及多种布瑞哌唑杂质以及相关研究分析,目前已知部分杂质包括:布瑞哌唑杂质1--50,布瑞哌唑亚砜,结构警示杂质布瑞哌唑氮氧化物等。
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Abemaciclib impurities
Abemaciclib, the third approved CDK4/6 inhibitor worldwide, was developed by Eli Lilly and Co. It has a broad indication covering early adjuvant therapy (32% reduction in risk of recurrence) ...
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Salbutamol Impurities
Impurity control is critical to ensuring Salbutamol‘s clinical safety. Impurities may originate from synthesis processes, storage degradation, or packaging materials, and their potential t...
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Vancomycin Impurity
SZEB specializes in supplying comprehensive vancomycin impurities compliant with EP/USP standards, accompanied by COA, NMR spectra, and traceability documentation. Our services include...
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Clarithromycin Impurities
Clarithromycin, the star drug in the macrolide antibiotic class, has quickly become a go-to choice in the field of anti-infectives since its successful development by Taisho in Japan back in 1984....
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Iopromide impurities
SZEB provides EP/USP certified impurities , isomers, degradation products, etc., providing complete COA, MS/NMR profiles to meet the requirements of FDA/EMA filing. Visit the ...
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Leuprorelin impurity
In 2025, Changchun Jinsai Pharmaceutical cooperated with Yida Bio to launch leuprolide injectable emulsion (Camcevi) in China, which is a 6-month long-acting, prefilled subcutaneous formulatio...
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Solution of Linaclotide impurities
As the competition for generic linaclotide has heated up,controling impurity has become the core link for companies to break through technical barriers and capture the market. ...
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Contrast Agent Medication I: Iopromide
Iopromide is a tri-iodinated, non-ionic, water-soluble X-ray contrast agent widely used in the field of medical imaging diagnostics. It enhances the imaging effects of devices like X-rays and CT...
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Cefcapene Impurity
Cefcapene, as a third-generation cephalosporin antibiotic, has become an important research target in the field of anti-infectives due to its unique chemical structure and broad-spectrum antibacteria...
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Cefprozil impurity
SZEB specialize in providing Cefprozil impurities, degradation products and related standards, strictly following USP/EP standards, with purity ≥98%, accompanied by complete COA certific...
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