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HEXACHLOROACETONE |
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PRODUCT IDENTIFICATION |
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CAS NO. |
116-16-5 |
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EINECS NO. | 204-129-5 | |
FORMULA | CCl3COCCl3 | |
MOL WT. | 264.75 | |
H.S. CODE | ||
TOXICITY |
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SYNONYMS | 1,1,1,3,3,3-hexachloropropan-2-one; Perchloroacetone; | |
1,1,1,3,3,3-Hexachloro-2-propanone; 1,1,1,3,3,3-Hexachloropropanone; Hexachloro-2-propanone; Bis(trichloromethyl) ketone; Hexachloropropanone; Perchloro-2-propanone; | ||
RAW MATERIALS |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE |
Clear liquid |
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MELTING POINT | 111 - 115 C | |
BOILING POINT |
208 - 212 C |
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SPECIFIC GRAVITY |
1.735 - 1.745 |
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SOLUBILITY IN WATER |
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pH | ||
VAPOR DENSITY | ||
AUTOIGNITION |
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NFPA RATINGS |
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REFRACTIVE INDEX |
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FLASH POINT | ||
STABILITY | Stable under ordinary conditions. | |
GENERAL DESCRIPTION APPLICATIONS |
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Hexachloroacetone is a haloketone consisting of two electron withdrawing groups (a ketone group and alpha-halogen substituent). The halogen substituent makes the carbon atom of the carbonyl group more electropositive. Haloketone reacts faster than n-alkylhloride in nucleophilic aliphatic substitution. Haloketones are important in substituted heterocycle compounds synthesis. Hantzsch Pyrrole Synthesis and the Hantzsch thiazole synthesis are examples. Haloketone are reagents for the preparation of regio- and stereoselective vinylic, allylic, or enamine compounds. In the crossed aldol reaction haloketone can be converted to halohydrin which subsequently forms an epoxide in presence of a base. |
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SALES SPECIFICATION | ||
APPEARANCE |
Clear liquid |
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ASSAY |
99.0% min |
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BOILING POINT |
660C - 70 C at 6mm Hg |
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TRANSPORTATION | ||
PACKING |
250kg in drum |
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HAZARD CLASS | 6.1 (Packing Group: III) | |
UN NO. | 2661 | |
OTHER INFORMATION |
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Hazard Symbols: XN N, Risk Phrases: 22-51/53, Safety Phrases: 24/25-61 |
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