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      "title": "3 Ingredient Natural Deordorant How To",
      "body": "This is a nice simple recipe for about 4 oz of natural homemade deodorant. The base recipe is only three ingredients, but I've included some common modifications for what some find a more luxurious end product. \n\n4oz Simple Natural Deodorant  (W/ Modifications):\n\n-1/2 Tablespoon Baking Soda\n-1/8 Cup Arrowroot Powder (Cornstarch works but arrowroot is preferred)\n-1/4 Cup Coconut Oil OR 1/8 Cup Cocoa Butter + 1/8 Cup Shea Butter\n(Some add about five drops of Vitamin E, but I tend not to. You can also use up to 40 drops of essential oil depending on variety and skin type, I err on the side of less for safety and subtlety personally.)\n\nProcess:\n\n1.  In any suitable container, gently melt your chosen fat source or sources to a liquid state.\n\n2. Discontinue heating and add your Baking Soda and Arrowroot Powder (or Cornstarch).\n\n3. Evenly stir your solution as it begins to cool, adding your Vitamin E and/or essential oil now if chosen.\n\n4. Transfer your well-blended liquid to one or two containers and allowed to cool before sealing.\n\nAll of the ingredients have pretty good shelf life so you end up with a nice decently shelf-stable product which will stay workable and nice at room temperature for a good time to come.  Schmidt's natural deodorant is made using a similar formula. I use my hands to apply after showering, but a popsicle stick should work well enough if you prefer an applicator. Enjoy!",
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      "title": "Producing Pyridine via Decarboxylation of Niacin",
      "body": "![image](https://img.esteem.ws/w808e6dt0b.jpg)\n\nThe following is a plain English technique for producing pyridine via the decarboxylation of niacin in the presence of a copper catalyst based on Nile Reds Youtube video. Make sure to familiarize yourself with all steps before attempting any synthesis or process work.\n\nRequired Substances & Equipment:\n\n50 Grams Niacin \n12 Grams Copper Carbonate \n3 Grams Sodium Hydroxides \nSimple Distillation Apparatus w/ 2x 250ml Round Bottom Flasks\nStirring Mantle\nVentilation / Chemical Respirator \nAmber Bottle\nMolecular Sieves \n\n1. 12 G of Copper Carbonate along with 50 G of Niacin are added to a mortar and pestle or food processor and ground until completely homogeneous. It is important that the mixture be evenly blended.\n\n2. Transfer finely ground and evenly blended Niacin / Copper Carbonate this is what powder to a 250 ml round bottom flask. Prepare your distillation apparatus for traditional distillation, with an additional round bottom flask prepared to receive the distilled Pyridine.\n\n ![image](https://img.esteem.ws/yfc3gomc4o.jpg)\n\n3. Place a heating mantle underneath your initial flask containing the Niacin blend and insulate the rest of the flask with foil or otherwise. Begin to slowly heat the powder, make sure you do not exceed 250° C my many degrees, niacin boils at 115° C. Progress will begins slowly, and complete distillation will take place over a scale of hours. The initial distillate recovered will be mostly Water or a Water / Pyridine blend. (Pyridine has off-putting and is toxic, you will require ventilation, and a respirator if you can smell it at all.)\n \nNote: white fume is an indicator the optimal distillation temperature have been exceeded, so lower your temperature if you see it. If the distillation is too slow, insulate the distillation head.\n\n4. Eventually distillation will slow to a stop and your receiving flask will contain an impure blend of Pyridine and Water. When no more distillate is recovered, separate the receiving flask from the apparatus, add 1 G of Sodium Hydroxide (Lye) to the solution and stirrer to react. The remaining Niacin should fall out of solution and it may form an aqueous layer. Separate using separatory funnel, vacuum filter or both if required. Discard your water layer if one has separated.\n\n5. To the filtered Pyridine solution, add another 2 G of Sodium Hydroxide to react any remaining Niacin and to pull out any remaining Water. Prepare your distillation apparatus with a fresh receiving flask and heat your Pyridine solution to 115° C. Distillation should be a bit smoother this time and leave a white slurry behind in your distilling flask.\n\n6. Store in amber glass with a couple grams of molecular sieves for dryness and safekeeping.\n\nThank you for reading!\n\nNileReds Pyridine video: https://youtu.be/r-xt24lBbrs",
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      "title": "Producing Pyridine via Decarboxylation of Niacin",
      "body": "![Decarboxylation.png](https://steemitimages.com/DQmYwfSCoAZ31ceUF7wGZkq61JjXXkMjD4eC7acqDaxNEZ8/Decarboxylation.png)\n\nThe following is a plain English technique for producing pyridine via the decarboxylation of niacin in the presence of a copper catalyst based on Nile Reds Youtube video. Make sure to familiarize yourself with all steps before attempting any synthesis or process work.\n\nRequired Substances & Equipment:\n\n50 Grams Niacin \n12 Grams Copper Carbonate \n3 Grams Sodium Hydroxides \nSimple Distillation Apparatus w/ 2x 250ml Round Bottom Flasks\nStirring Mantle\nVentilation / Chemical Respirator \nAmber Bottle\nMolecular Sieves \n\n- 12 G of Copper Carbonate along with 50 G of Niacin are added to a mortar and pestle or food processor and ground until completely homogeneous. It is important that the mixture be evenly blended.\n\n- Transfer finely ground and evenly blended Niacin / Copper Carbonate this is what powder to a 250 ml round bottom flask. Prepare your distillation apparatus for traditional distillation, with an additional round bottom flask prepared to receive the distilled Pyridine.\n\n![zubrick098.gif](https://steemitimages.com/DQmZx12VHGYXyDSuy63zku7iYFtQ94r3ERMc7WQptFVRyBM/zubrick098.gif)\n\n- Place a heating mantle underneath your initial flask containing the Niacin blend and insulate the rest of the flask with foil or otherwise. Begin to slowly heat the powder, make sure you do not exceed 250° C my many degrees, niacin boils at 115° C. Progress will begins slowly, and complete distillation will take place over a scale of hours. The initial distillate recovered will be mostly Water or a Water / Pyridine blend. (Pyridine has off-putting and is toxic, you will require ventilation, and a respirator if you can smell it at all.)\n \nNote: white fume is an indicator the optimal distillation temperature have been exceeded, so lower your temperature if you see it. If the distillation is too slow, insulate the distillation head.\n\n- Eventually distillation will slow to a stop and your receiving flask will contain an impure blend of Pyridine and Water. When no more distillate is recovered, separate the receiving flask from the apparatus, add 1 G of Sodium Hydroxide (Lye) to the solution and stirrer to react. The remaining Niacin should fall out of solution and it may form an aqueous layer. Separate using separatory funnel, vacuum filter or both if required. Discard your water layer if one has separated.\n\n- To the filtered Pyridine solution, add another 2 G of Sodium Hydroxide to react any remaining Niacin and to pull out any remaining Water. Prepare your distillation apparatus with a fresh receiving flask and heat your Pyridine solution to 115° C. Distillation should be a bit smoother this time and leave a white slurry behind in your distilling flask.\n\n- Store in amber glass with a couple grams of molecular sieves for dryness and safekeeping.\n\nThank you for reading!\n\nNileReds Pyridine video: https://m.youtube.com/watch?v=r-xt24lBbrs",
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