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| TRIFLUOROACETALDEHYDE HYDRATE Basic information |
| Product Name: | TRIFLUOROACETALDEHYDE HYDRATE | | Synonyms: | Trifluoroacetaldehyde hydrate (diol), Tech.;Trifluoroethanal hydrate;TRIFLUOROACETALDEHYDE HYDRAT;Trifluoracetaldehyde monohydrate,~75% in water;Trifluoroacetaldehyde hydrate, technical, 75%;Trifluoroacetaldehyde monohydrate, 75% aqueous solution;2,2,2-Trifluoro-1,1-ethanediol (contains Total ca. 25% Water);2,2,2-Trifluoro-1,1-ethanediol (contains Total ca. 35% Water) | | CAS: | 421-53-4 | | MF: | C2H3F3O2 | | MW: | 116.04 | | EINECS: | 207-006-4 | | Product Categories: | | Mol File: | 421-53-4.mol |
| TRIFLUOROACETALDEHYDE HYDRATE Chemical Properties |
| Hazard Codes | T | | Risk Statements | 20/21/22-43-36-22-11 | | Safety Statements | 24/25-36/37-26-16 | | RIDADR | 1989 | | Hazard Note | Toxic | | TSCA | Yes | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29130000 | | Toxicity | LD50 oral in mouse: 600mg/kg |
| TRIFLUOROACETALDEHYDE HYDRATE Usage And Synthesis |
| Chemical Properties | colourless liquid | | Uses | Trifluoroacetaldehyde monohydrate is used as an agricultural
chemical, a drug and therapeutic agent, a fungicide, bactericide,
and wood preservative. | | Uses | One general application of trifluoroacetaldehyde is the preparation of trifluoroethylamino derivatives via reductive amination reaction. This synthesis includes the formation of the corresponding N,O-acetal intermediates followed by their reduction using NaBH4?or 2-picoline borane complex, affording the target trifluoroethylamino compounds in moderate to good yields. Another general application of trifluoroacetaldehyde is the synthesis of chiral α-substituted trifluoroethylamino compounds. | | Safety Profile | Moderately toxic by ingestion,intravenous, and intraperitoneal routes. When heated todecomposition it emits very toxic fumes of F??. |
| TRIFLUOROACETALDEHYDE HYDRATE Preparation Products And Raw materials |
| Raw materials | Ethanol, 2,2,2-trifluoro-1-(2,2,2-trifluoroethoxy)--->TRIFLUOROACETALDEHYDE-->1,1,1-trifluoro-3-nitropropane-->Phenyl (trifluoromethyl) sulfone-->Trifluoroacetonitrile-->1,1,1-TRIFLUOROPROPANE-->Acetaldehyde-->TRIFLUOROACETALDEHYDE ETHYL HEMIACETAL-->2,2,2-Trifluoroethanol-->Trifluoroacetic acid-->Trifluoromethane-->Formaldehyde-->Trifluoroacetic anhydride |
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