SabbathViper
Greenlighter
- Joined
- Feb 2, 2012
- Messages
- 28
My 250ul micro-pipette will be here tomorrow, and my 20mg 25C-NBOMe HCL is already here. Unfortunately it was shipped in a baggie rather than a nice glass vial, so I am worried that some residue will account for product loss overall when measured on the mg scale. Anyways!
I plan to dissolve the 20mg into 20ml of water in a 1:1 ratio, then use the micro-pipette to perfectly measure out 250ul/ug doses for placement either in microvials (for dosing intranasal) or on blotters for buccal/sublingual.
My fear is this: when dissolving the NBOMe into water, and siphoning it out - how do I know that it isn't concentrated more in particular areas of the liquid than others? For example, how do I know that one 250ul sample from the solution isn't more potent than the next? Obviously constant and vigorous stirring will keep things moving, but is it safe to assume that it is fairly evenly distributed in a 1:1 ratio in the water?
I want to be a safe, accurate, and methodical as possible for my sake and that of my friends.
I plan to dissolve the 20mg into 20ml of water in a 1:1 ratio, then use the micro-pipette to perfectly measure out 250ul/ug doses for placement either in microvials (for dosing intranasal) or on blotters for buccal/sublingual.
My fear is this: when dissolving the NBOMe into water, and siphoning it out - how do I know that it isn't concentrated more in particular areas of the liquid than others? For example, how do I know that one 250ul sample from the solution isn't more potent than the next? Obviously constant and vigorous stirring will keep things moving, but is it safe to assume that it is fairly evenly distributed in a 1:1 ratio in the water?
I want to be a safe, accurate, and methodical as possible for my sake and that of my friends.

