Search results
Results from the WOW.Com Content Network
DCM is produced by treating either chloromethane or methane with chlorine gas at 400–500 °C. At these temperatures, both methane and chloromethane undergo a series of reactions producing progressively more chlorinated products.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Vinyl trichloride: Polycarbonate (PC) Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Polystyrene (PS) Acetone: Ethylene dichloride (EDC) Methylene chloride: Methyl ethyl ketone (MEK) Toluene: Xylene: Polyvinyl chloride (PVC) Acetone: Cyclohexane ...
Paraquat (trivial name; / ˈ p ær ə k w ɒ t /), or N,N′-dimethyl-4,4′-bipyridinium dichloride (systematic name), also known as methyl viologen, is a toxic organic compound with the chemical formula [(C 6 H 7 N) 2]Cl 2. It is classified as a viologen, a family of redox-active heterocycles of similar structure. [5]
Methyldichloroarsine, sometimes abbreviated "MD" and also known as methyl Dick, [1] is an organoarsenic compound with the formula CH 3 AsCl 2. This colourless volatile liquid is a highly toxic vesicant that has been used in chemical warfare .
Phase behavior Triple point? K (? °C), ? Pa Critical point [6]: 510 K (237 °C), 6100 kPa Std enthalpy change of fusion, Δ fus H o +6.160 kJ/mol Std entropy change
Methylphosphonyl dichloride (DC) or dichloro is an organophosphorus compound. It has commercial application in oligonucleotide synthesis, [1] but is most notable as being a precursor to several chemical weapons agents. It is a white crystalline solid that melts slightly above room temperature. [2]
This page was last edited on 19 January 2023, at 06:35 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.