CAS 946504-83-2 · Fluorinated Compound · 3 functional traits · cGMP compliant · Ships from USA in 2-3 days
benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate (CAS Number: 946504-83-2) is a fluorine-containing building block with enhanced metabolic stability featuring a Piperidine ring. ChemContract Research supplies this moderate-complexity compound in high purity from our Huntington Beach, California facility, ensuring consistent quality and reliable domestic delivery throughout the United States.
The carbon–fluorine bond is the strongest single bond to carbon (485 kJ/mol). This exceptional stability underpins the "fluorine scan" strategy used in medicinal chemistry to optimize drug candidates. The piperidine ring is the most common nitrogen heterocycle in FDA-approved drugs, appearing in over 70 marketed pharmaceuticals across CNS, cardiovascular, and oncology indications. Hydroxyl groups are critical pharmacophores — they serve as hydrogen-bond donors and acceptors, influencing drug–target binding, aqueous solubility, and metabolic susceptibility.
Primary applications include metabolic blocking strategy — fluorine substitution to improve drug half-life and cns drug scaffold (present in donepezil, methylphenidate, fentanyl class). This compound serves researchers and manufacturers across the pharmaceutical, diagnostic imaging, agrochemical sectors. Whether you require benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate for early-stage research, process development, or commercial-scale production, ChemContract Research offers flexible ordering from milligram to multi-kilogram quantities with custom synthesis options and full batch documentation including Certificates of Analysis (CoA) and Safety Data Sheets.
How benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate is used across pharmaceutical and diagnostic imaging sectors
Metabolic blocking strategy — fluorine substitution to improve drug half-life
CNS drug scaffold (present in donepezil, methylphenidate, fentanyl class)
Mitsunobu reaction substrate for stereospecific inversion at chiral centers
PET radiotracer precursor ([¹⁸F]-labeling) for diagnostic imaging
Conformationally-restricted amine for receptor binding optimization
Oxidation to aldehydes (Swern, Dess–Martin) or ketones for downstream chemistry
Detailed specifications for this fluorinated compound, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:
Handle with care in a well-ventilated fume hood. Some fluorinated compounds may release HF upon decomposition. Use chemical-resistant gloves. Handle with standard precautions. Piperidine and some derivatives have strong amine odors. Use a fume hood. Handle with standard precautions. Some alcohols are flammable. Use adequate ventilation and appropriate PPE.
Store at recommended temperature in a tightly sealed container. Protect from moisture, heat, and incompatible materials. Store at room temperature in a well-sealed container. Some N-unsubstituted piperidines are volatile. Store at room temperature in a tightly sealed container away from heat sources and oxidizers.
Fluorinated compounds require careful handling. We provide benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate with verified fluorine content, stability data, and guidance on storage to prevent decomposition.
Every batch of benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate is produced under cGMP conditions with full CoA documentation, HPLC purity verification, and lot traceability.
Ship from our Huntington Beach, CA facility with 2-3 business day domestic delivery. No import delays, no customs fees, no tariff surprises.
Need a specific grade, quantity, or derivative of benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.
Common questions about benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate
benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate is a fluorine-containing building block with enhanced metabolic stability used primarily in the pharmaceutical and diagnostic imaging industries. Key applications include metabolic blocking strategy — fluorine substitution to improve drug half-life and cns drug scaffold (present in donepezil, methylphenidate, fentanyl class).
ChemContract Research is a trusted USA-based supplier of benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.
ChemContract Research supplies benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.
Yes. ChemContract Research offers custom synthesis services for benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.
The Piperidine ring system(s) in benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate is a privileged structure in medicinal chemistry, appearing in numerous FDA-approved drugs. This scaffold is commonly used in kinase inhibitor design, GPCR modulator development, and lead optimization programs. ChemContract supplies this building block for early-stage discovery through process-scale manufacturing.
The fluorine atom(s) in benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate confer several advantages in drug design: increased metabolic stability due to the strong C–F bond (485 kJ/mol), enhanced lipophilicity for improved membrane permeability, and potential for favorable electrostatic interactions with biological targets. These properties make fluorinated compounds like benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate valuable in pharmaceutical development.
Store at recommended temperature in a tightly sealed container. Protect from moisture, heat, and incompatible materials. Store at room temperature in a well-sealed container. Some N-unsubstituted piperidines are volatile. Store at room temperature in a tightly sealed container away from heat sources and oxidizers. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.
The CAS Registry Number for benzyl 4-hydroxy-4-(trifluoromethyl)piperidine-1-carboxylate is 946504-83-2. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.
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