Product Details:
Payment & Shipping Terms:
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CAS Number: | 96096-55-8 | Purity: | 96% |
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Color: | White | Formula: | C28H44O2 |
Appearance: | Powder | Other Names: | 3-meo-mipt |
High Light: | psychedelic research chemicals,hallucinogenic research chemicals |
1. Details
Pro Name |
3meo
|
CAS NO
|
96096-55-8 |
IUPAC name
|
N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-methylpropan-2-amine |
Molecular Formula |
C15H22N2O
|
Appearance
|
White or Similar crystalline powder |
Delivery Time
|
Within 2 days after receive payment |
PackAge
|
Aluminum foil bag |
Port
|
Hongkong |
Production Capacity
|
500 Kilogram/Month |
Purity
|
99.5% |
Storage
|
store in dry and cool place. |
LimitNum
|
10 Gram |
Application
|
For lab research |
Color
|
White |
It is worth noting that compounds of the NBOMe class are not orally active and should, therefore, be taken sublingually by simply placing the substance into one's mouth and allowing it to absorb over a period of 30 minutes slowly.
be vaporized and inhaled; this may cause significantly quicker effects and shorter duration as is expected from that route of administration. However, this route of administration is not recommended, unless using precise liquid measurement, due to the difficulties of measuring and handling substances active in the microgram range.
In comparison to 2C-I, the addition of an NBOMe group to the structure results in a sixteen-fold increase in potency, allowing even the most extreme of dosages to fit in liquid form onto tabs and blotter paper, which people often mistake for LSD. 25i-NBOMe has a distinctly bitter and metallic taste that LSD does not have, which can be useful in determining what substance is really on the blotter.
psychedelic drug and derivative of the psychedelic phenethylamine 2C-C. 25C-NBOMe appeared on online vendor sites in 2010 but was not reported in the literature until 2011.[1] It acts as a potent partial agonist for the 5HT2A receptor,[2] and has been studied in its 11C radiolabelled form as a potential ligand for mapping the distribution of 5-HT2A receptors in the brain, using positron emission tomography (PET).
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