- 1,1,3-Trichloroacetone
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- $35.00 / 1kg
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2024-03-29
- CAS:921-03-9
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 1,1,3-Trichloroacetone Basic information |
| Product Name: | 1,1,3-Trichloroacetone | | Synonyms: | 1,1,3-TRICHLORO-2-PROPANONE;1,1,3-TRICHLOROACETONE;1,1,3-TCA;1,1,3-TRICHLOROACETONE, WACKER QUALITY;2-Propanone, 1,1,3-trichloro-;1,1,3-TRICHLOROPROPANONE;1,1,3-TrichL;1,1,3-trichloro-2-propanon | | CAS: | 921-03-9 | | MF: | C3H3Cl3O | | MW: | 161.41 | | EINECS: | 213-063-6 | | Product Categories: | 1 | | Mol File: | 921-03-9.mol |  |
| | 1,1,3-Trichloroacetone Chemical Properties |
| Melting point | 9-11 °C(lit.) | | Boiling point | 88-90 °C76 mm Hg(lit.) | | density | 1.512 g/mL at 20 °C(lit.) | | vapor pressure | 30-350Pa at 20-50℃ | | refractive index | n20/D 1.491 | | Fp | 80 | | storage temp. | Refrigerator, under inert atmosphere | | solubility | Chloroform, Methanol | | form | Oil | | color | Clear Colourless | | BRN | 1746647 | | InChIKey | ZWILTCXCTVMANU-UHFFFAOYSA-N | | LogP | 0.45 | | CAS DataBase Reference | 921-03-9(CAS DataBase Reference) | | NIST Chemistry Reference | 2-Propanone, 1,1,3-trichloro-(921-03-9) |
| Hazard Codes | T+,N | | Risk Statements | 25-26-34-50/53-68-21 | | Safety Statements | 26-36/37/39-45-60-61-28 | | RIDADR | UN 3390 6.1/PG 1 | | WGK Germany | 3 | | RTECS | UC3840000 | | HazardClass | 6.1(b) | | PackingGroup | III | | HS Code | 29147000 | | Toxicity | mmo-sat 50 mL/plate ENMUDM 7,163,85 |
| | 1,1,3-Trichloroacetone Usage And Synthesis |
| Description | 1,1,3-Trichloroacetone is direct-acting mutagens in the Ames/Salmonella assay. It is precursor for the generation of 1,3-dihalo oxyallyl intermediates, which undergo [4 + 3] cycloadditions with a host of 1,3-diene systems. | | Chemical Properties | Light yellow transparent liquid | | Uses | 1,1,3-Trichloroacetone is a reagent used to synthesize chlorinated 5-hydroxy-4-methyl-2(5H)-furanones and mucochloric acid. In addition, it can also be used to synthesize (+)-Phorbol. Phorbol derivatives are important for biomedical research and capable of stimulating T-cell activation, proliferation and cytokine production. | | Uses | 1,1,3-Trichloroacetone was used in base-induced solvolyses of [3.2.1]Bicyclic α,α′-dichloro ketones. | | Safety Profile | Poison by inhalation. Corrosiveand lachrymator. Mutation data reported. Combustibleliquid. When heated to decomposition it emits toxic fumesof Clí. |
| | 1,1,3-Trichloroacetone Preparation Products And Raw materials |
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