INTRODUCTION
Trichloroacetonitrile is a halogenated organic compound belonging to nitrile family. Its strong electrophilic character makes it a valuable intermediate in organic synthesis. It readily undergoes hydrolysis, particularly under acidic or basic conditions, yielding trichloroacetamide and related derivatives.
MANUFACTURE
Trichloroacetonitrile is typically produced through controlled chlorination of acetonitrile. This involves free radical substitution, where hydrogen atoms on the methyl group are progressively replaced by chlorine. Alternative approach involves dehydration of trichloroacetamide.
| Synonyms | Cyanotrichloromethane; 2,2,2-Trichloroacetonitrile; NSC 66405 |
| CAS no. | 545-06-2 |
| EINECS no. | 208-885-7 |
| Molecular formula | C2Cl3N |
| Molecular weight | 144.39 |
| Structure |  |
APPLICATIONS
Trichloroacetonitrile is a valuable intermediate with a range of applications. Its utility comes from presence of two strong electron withdrawing groups (CCl3 and CN), which allow diverse chemical transformations.
| Pharmaceutical Intermediates: |
| • Used in the synthesis of heterocyclic compounds (e.g., imidazoles, triazines, pyrimidines, oxadiazoles, etc). |
| • Acts as a building block for API intermediates, especially where strong electron-withdrawing groups are required. |
| • Useful in cyanation reactions to introduce nitrile functionality into drug molecules. |
| Agrochemical Applications: |
| • Serves as an intermediate in the synthesis of Herbicides, Fungicides and Insecticides. |
| • Enables synthesis of chlorinated nitrile-based bioactive molecules. |
| • Used in developing crop protection agents due to its reactivity toward nucleophiles. |
| Organic Synthesis & Fine Chemicals: |
| • Functions as a reactive nitrile source in multi-step synthesis. |
| • Used in C-C and C-N bond formation reactions. |
| • Acts as a precursor for: amides, carboxylic acids (via hydrolysis), amidines and imidates. |
| Heterocyclic Chemistry: |
| Acts as a key reagent for preparation of: |
| • Nitrogen-containing heterocycles. |
| • Fused ring systems. |
| • Facilitates ring closure reactions due to its activated nitrile group. |
SPECIFICATIONS
| Test | Unit | Specification |
|---|---|---|
| Appearance | – | Colourless yellow-brown liquid, free from visible impurities |
| Identification (by IR) | – | Should conform to the structure |
| Purity (by GC): | – | |
| Trichloroacetonitrile | % | NLT 98.5 |
| Single Unknown Impurity | % | NMT 0.5 |
| Moisture (by KF) | % | NMT 0.1 |
STORAGE & PRECAUTION
Keep container tightly closed. Store in well-ventilated area.
PACKING
UN Approved drums;
Packaging quantities (net weight/volume per container): 30 kg/drum, 250 kg/drum
Primary Packaging (material of construction of packaging and closure): Plastic drums
REACH Status
Not registered
ExSyn offers Trichloroacetonitrile on a commercial scale and welcomes your enquiries. Regardless of the quantity required, our commitment to exceptional quality and reliable service makes ExSyn the preferred supplier of choice. Should you require any additional information or the SDS, please feel free to contact us.
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