Keywords

• Methyl 2-hydroxy-3-methoxy-3,3-diphenylpropanoate
• 178306-47-3
• Ambrisentan Impurity

Quick Details

• ProName: Benzenepropanoic acid,a-hydroxy-b-met...
• CasNo: 178306-47-3
• Molecular Formula: C17H18O4
• 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

Ambrisentan Impurity Reference Standard
Utilized in pharmaceutical R&D, quality control, and regulatory submissions as an analytical standard to detect and quantify impurities in drug substances, ensuring drug safety and efficacy.

High Purity Assurance：Synthesized and purified under rigorous protocols to ensure single-component impurities.

Regulatory Compliance：Adheres to USP, EP, BP pharmacopeia standards, supporting global regulatory filings.

Stability：Stable for up to 3 years when stored at -20°C.

Storage：Store at -20°C, protected from light and moisture.

Shipping：Transported under cryogenic conditions (dry ice or cold chain) to maintain stability.

application area ：

Impurity profiling in new drug development

Process optimization and quality control in drug manufacturing

Generic drug bioequivalence studies