Keywords

• N-(-2-[3,4-Dimethoxyphenyl]ethyl)-3,4-dimethoxy-N-methylbenzeneethanamine
• Dobutamine Impurity
• 33978-72-2

Quick Details

• ProName: YS-035 HCL
• CasNo: 33978-72-2
• Molecular Formula: C21H29NO4
• Appearance: off-white powder
• Application: Pharmaceutical research
• DeliveryTime: prompt delivery
• PackAge: Screw bottle,foil bags,Reagent bottles
• Port: shenzhen/hongkong
• ProductionCapacity: 5000 Metric Ton/Year
• Purity: 95%+
• Storage: cool and dry
• Transportation: DHL,FedEx,UPS,EMS,TNT;
• LimitNum: 1 Kilogram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

We supply over 20000 types of spot impurity reference materials, with sufficient supply and same day delivery to meet customers' urgent needs for replenishment at any time. The company has its own research and development center and laboratory, and the team members have over ten years of experience in developing drug impurity reference standards. Our website www.molcoo.com covers over 98% of cutting-edge generic drug projects, with complete structural formulas that greatly save customers time in impurity structure analysis and inference. All products undergo strict quality control testing and provide relevant information such as COA, H-NMR, C-NMR, MS/GC-MS, HPLC/GC purity, QNMR quantification, TGA thermogravimetric analysis, IR infrared, UV ultraviolet, two-dimensional (COSY, NOESY, HMBC, HMQC), etc. These structural confirmation spectra ensure quality and reliability. Our products have a wide range of categories, fast delivery time, good quality, and low prices, which can quickly solve various customer needs such as replenishment and consistency evaluation.

Details

Dobutamine impurity reference standards are crucial tools for drug development and quality control. These reference standards ensure that the impurity levels in dobutamine drugs comply with international standards and regulations, thereby guaranteeing the safety and effectiveness of the drugs.

We offer a variety of dobutamine impurity reference standards, including but not limited to Dobutamine Impurity 5, DOBUTAMINE EP Impurity C, and others. These reference standards have undergone rigorous quality control to ensure their purity and stability.

By using dobutamine impurity reference standards, drug developers and quality control personnel can accurately identify and quantify impurities in the drugs, ensuring that their quality meets relevant standards and regulations.

We are committed to providing our customers with high-quality dobutamine impurity reference standards to meet their needs in drug development and quality control. Please feel free to contact us with any questions or requirements.