FriendlyFinger
(Hive Bee) 07-21-03 04:48 No 448746 |
propionyl chloride via Cyanuric chloride. ?? | Bookmark | ||||||
What's the advantage of making acid chlorides via CC? So far I know that Thionyl chloride is available and relativly inexpensive, but corrosive and also listed as a chemical warefare agent. Phosphours tri and pentchloride have been called "anti-social" chemicals on the hive. What does that mean, too much smell or HCL? S2Cl2 look dificult. I've read about using Cyanuric cloride, but from what I understand you need equal mole amounts of TEA and the carboxylic acid and 1/2 mole of CC. I'm serching as much as I can but am a bit confused about which way to go. Regards, FF |
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Osmium (Stoni's sexual toy) 07-29-03 13:22 No 450540 |
Just guessing, but I think CC might be easier... | Bookmark | ||||||
Just guessing, but I think CC might be easier to handle and less suspicious (?). Thionyl and the P chlorides might arouse suspicions due to their possible uses in drug and chemical weapons syntheses. I'm not fat just horizontally disproportionate. http://www.whatreallyhappened.com |
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