T
theking
Guest
Hi there,
I've read a bit on the E1/E2 tests, but was after some more specifics. What I'd like to know is exactly how these tests work.
Firstly, what happens if you have a pill with a combination of chemicals in it? Say, MDxx and speed? Which turn the reagent different colours. Does the reagent become a mixture of the two different colours?
Does the dominant chemical override this turning the reagent soley that colour? Or will the result be skewed towards the dominant colour (not completely one colour or the other, and not in the middle either, but rather closer towards the colour of the dominant chemcial, with hints of the other chiemical's colour)?
(If that all makes sense
Secondly, I've seen some different info around as to what each test can identify.
One of them mentions herion, another one using the same reagent makes no mention of this, etc etc. The erowid faq on E testing has a rather extensive list of identifable substances. What I'm guessing here (And I think I read it somewhere), is that the tests test for a class of compounds rather than specific compounds, correct? And that the indetifable compounds listed are perhaps the most common ones found in each class.
eg, 2C-B...this is a phenethylamine, so if the test becomes the colour for 2C-B, does this mean 2C-B is present, or ANY phenethylamine? (Including DOB and DOM). I suspect this is the case. So acutally, the colours identify drug classes/families rather than indiviual compounds.
In this sense, the erowid faq listing lots of other compounds suggests that the colour change will be slightly different for each compound of a specific family. Which sounds like it would make sense.
Comments, suggestions, help?
Thanks,
Josh
I've read a bit on the E1/E2 tests, but was after some more specifics. What I'd like to know is exactly how these tests work.
Firstly, what happens if you have a pill with a combination of chemicals in it? Say, MDxx and speed? Which turn the reagent different colours. Does the reagent become a mixture of the two different colours?
Does the dominant chemical override this turning the reagent soley that colour? Or will the result be skewed towards the dominant colour (not completely one colour or the other, and not in the middle either, but rather closer towards the colour of the dominant chemcial, with hints of the other chiemical's colour)?
(If that all makes sense
Secondly, I've seen some different info around as to what each test can identify.
One of them mentions herion, another one using the same reagent makes no mention of this, etc etc. The erowid faq on E testing has a rather extensive list of identifable substances. What I'm guessing here (And I think I read it somewhere), is that the tests test for a class of compounds rather than specific compounds, correct? And that the indetifable compounds listed are perhaps the most common ones found in each class.
eg, 2C-B...this is a phenethylamine, so if the test becomes the colour for 2C-B, does this mean 2C-B is present, or ANY phenethylamine? (Including DOB and DOM). I suspect this is the case. So acutally, the colours identify drug classes/families rather than indiviual compounds.
In this sense, the erowid faq listing lots of other compounds suggests that the colour change will be slightly different for each compound of a specific family. Which sounds like it would make sense.
Comments, suggestions, help?
Thanks,
Josh
