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| | Chloropyrilene Basic information |
| Product Name: | Chloropyrilene | | Synonyms: | Ccris 4768;Chloromethapyrilene;CHLOROPYRILINE;Chlorothenylpyramine;N-(5-Chloro-2-thenyl)-N',N'-dimethyl-N-(2-pyridyl)ethylenediamine;NCI-C-60559;Pyrithen;Tagathen | | CAS: | 148-65-2 | | MF: | C14H18ClN3S | | MW: | 295.83 | | EINECS: | | | Product Categories: | | | Mol File: | 148-65-2.mol |  |
| | Chloropyrilene Chemical Properties |
| Melting point | 25°C | | Boiling point | bp1.0 155-156° | | density | 1.2682 (rough estimate) | | refractive index | 1.6100 (estimate) | | pka | pKa 8.4 (Uncertain) | | Water Solubility | 2.012g/L(37.5 ºC) | | EPA Substance Registry System | Chlorothen (148-65-2) |
| | Chloropyrilene Usage And Synthesis |
| Definition | ChEBI: Chloropyrilene is a dialkylarylamine and a tertiary amino compound. | | General Description | Colorless liquid. | | Air & Water Reactions | Slightly water soluble . | | Reactivity Profile | A base. An organosulfide and an amine. Organosulfides are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. | | Fire Hazard | Flash point data for Chloropyrilene are not available, but Chloropyrilene is probably combustible. |
| | Chloropyrilene Preparation Products And Raw materials |
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