Trifluoroacetamide CAS 354-38-1

① Acts Trifluoroacetamide as key trifluoromethyl building block for pharmaceutical synthesis, introducing CF₃-CO-NH- group to prepare anti-tumor and antiviral drugs in fine chemical production.
② Serves Trifluoroacetamide CAS 354-38-1 as acylating reagent and fluorinating intermediate for organic synthesis, promoting amidation and trifluoromethylation reactions in agrochemical manufacturing.
③ Functions as catalyst ligand and electrolyte additive, improving reaction efficiency and battery performance in chemical catalysis and new energy fields.

Store Trifluoroacetamide CAS 354-38-1 at 5-25℃ in sealed HDPE/amber glass drums in cool, dry, well-ventilated area, away from open fire, strong oxidants, strong acids/alkalis and direct sunlight. Wear nitrile gloves, safety goggles and dust mask; avoid inhalation, skin/eye contact & ingestion (mild irritant). Reseal tightly post-use to prevent moisture absorption, caking and oxidation. Dispose as hazardous waste; transport as non-hazardous solid, moisture-proof anti-extrusion packaging, no cold chain, avoid mixing with acids/alkalis/oxidants and high-temp exposure.

✅ High Trifluoroacetamide trifluoromethyl reactivity with amide active group, excellent solubility in polar solvents, stable crystalline structure under sealed storage, no self-decomposition risk in normal conditions.
✅ High Trifluoroacetamide CAS 354-38-1 reaction selectivity, low dosage achieves efficient trifluoromethylation/amidation, no toxic by-products, broad applicability for pharmacy/agrochemicals/catalysis.
✅ Cost-effective industrial mass production, stable batch purity, easy dissolution and operation, compliant with REACH/ISO standards, ideal for fluorine chemical synthesis.

- Hazard Class：Non-hazardous | HS Code：2915900090
- Non-flammable | No UN number | Decomposes on overheating
- Hazard Statements：H315 (skin irritation), H319 (eye irritation), H335 (respiratory irritation)
- Precaution Statements：P261, P280, P305+351+338, P332+313