clamshavefeelingstoo
Rising Star
I would like to know the relative risks of working around various solvents. Given that one would take every precaution to ventilate and minimize exposure anyways, what solvents might be best in terms of efficiency in performance but also being least toxic?
A hypothetical A/B extraction would require a defat NP, an extracting NP, and optionally IPA or another solvent besides h2o for the initial stew. I've heard of DCM being relatively non-toxic for being a moderately strong-pulling solvent (high xlogp), so I'm assuming DCM could be used as the extracting NP (if you wanted to include a wider spectrum of alkaloids). What would you consider to be a good, safe defat NP? Since Limonene has a high xlogp and can be food-grade, is this ideal for defatting? Toluene, Xylene, and Naphtha are all rather toxic, and chloroform cannot be obtained readily. The rest are probably too weak, no?
A hypothetical A/B extraction would require a defat NP, an extracting NP, and optionally IPA or another solvent besides h2o for the initial stew. I've heard of DCM being relatively non-toxic for being a moderately strong-pulling solvent (high xlogp), so I'm assuming DCM could be used as the extracting NP (if you wanted to include a wider spectrum of alkaloids). What would you consider to be a good, safe defat NP? Since Limonene has a high xlogp and can be food-grade, is this ideal for defatting? Toluene, Xylene, and Naphtha are all rather toxic, and chloroform cannot be obtained readily. The rest are probably too weak, no?