2-Bromobenzotrifluoride

Min.Order / FOB Price:Get Latest Price

1 Kilogram	FOB Price: USD 10.0000

1 Kilogram

FOB Price: USD 10.0000

Min.Order :1 Kilogram
Purity: 95%+
Payment Terms : T/T,Other

Keywords

o-Bromobenzotrifluoride Toluene, alpha,alpha,alpha-trifluoro-2-bromo- 2-Brombenzotrifluorid [Czech]

Quick Details

Appearance:White solid
Application:Pharmaceutical research
PackAge:Screw bottle,foil bags,Reagent bottles
ProductionCapacity:5000|Metric Ton|Year
Storage:cool and dry
Transportation: DHL,FedEx,UPS,EMS,TNT;

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:

Corporate Strengths

Technical Expertise: In-house R&D center and laboratories with over a decade of experience in impurity R&D.
Product Portfolio: Over 20,000 in-stock impurity reference standards covering 98%+ of cutting-edge generic drug projects.
Quality Assurance: Stringent QC system with optional third-party testing (e.g., QNMR, TGA).
Service Capabilities: Custom synthesis, impurity isolation, and process optimization supporting the entire drug development lifecycle.

Applications

Drug Development: Impurity profiling, structural verification, and quality standard establishment.
Consistency Evaluation: Meeting CDE requirements for post-approval changes, accelerating generic drug approvals.
Process Optimization: Impurity source analysis and critical process parameter validation.

Collaboration Support

Technical Assistance: Spectra interpretation, synthetic route design, and other value-added services.
Logistics: Cold-chain shipping to maintain product stability.
Custom Solutions: Tailored services for novel molecules and complex impurities.

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