Keywords

• 1H-Indol-5-ol,3-(2-aminoethyl)-, monohydrochloride (9CI)
• Indol-5-ol, 3-(2-aminoethyl)-,monohydrochloride (8CI)
• 3-(2-Aminoethyl)-1H-indol-5-ol hydrochloride

Quick Details

• ProName: Serotonin hydrochloride
• CasNo: 153-98-0
• Molecular Formula: C10H12N2O.HCl
• Appearance: white or almost white crystalline powd...
• Application: Pharmaceutical research
• DeliveryTime: prompt delivery
• PackAge: food packages,foil bags
• Port: shenzhen/hongkong
• ProductionCapacity: 500 Gram/Year
• Purity: 95%+
• Storage: cool and dry
• Transportation: DHL,FedEx,UPS,EMS,TNT;
• LimitNum: 10 Milligram
• 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

Melatonin EP Impurity Reference Standards

Melatonin EP impurity reference standards are essential tools in the fields of drug research and development, quality control, and impurity analysis. These reference standards cover a variety of impurities that may be generated during the production of melatonin, including Melatonin EP Impurity A (Melatonin Impurity 15), Melatonin EP Impurity C, Melatonin EP Impurity D, and others. These reference standards are characterized by high purity, stability, and sensitivity, accurately reflecting the impurity situation in drugs and providing strong support for drug quality control.

By using Melatonin EP impurity reference standards, researchers can easily identify and quantify the impurity content in drugs, thereby ensuring the safety and effectiveness of the drugs. Furthermore, these reference standards can be used to optimize drug production processes, improve drug purity and stability, and reduce production costs.

Our Melatonin EP impurity reference standards undergo rigorous quality control to ensure compliance with international pharmacopoeias and relevant regulations. We offer a range of specifications and packaging options to meet the needs of different customers.