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4-Methoxyamphetamine (hydrochloride)

Item № 12041
CAS № 3706-26-1
Purity ≥98%

Formulation:  A crystalline solid

SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL
     5 mg $35.00 0.00
     10 mg $67.00 0.00
     50 mg $280.00 0.00

Pricing updated 2019-03-26. Prices are subject to change without notice.

Description
Synonyms
  • 4-MA
  • p-MA
  • para-Methoxyamphetamine
  • PMA

4-Methoxyamphetamine (4-MA), is a serotonergic drug of the amphetamine class.1 4-MA exhibits both structural and pharmacological similarity to 3,4-methylenedioxymethamphetamine and may be a more potent hallucinogen, particularly through its effects on serotonergic transmission and through reversible inhibition of the enzyme MAO-A.1,2,3,4 This product is intended for research and forensic applications.

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Technical Information
Formal Name
4-methoxy-α-methyl-benzeneethanamine, monohydrochloride
CAS Number
3706-26-1
Synonyms
  • 4-MA
  • p-MA
  • para-Methoxyamphetamine
  • PMA
Molecular Formula
C10H15NO • HCl
Formula Weight
201.7
Purity
≥98%
Formulation
A crystalline solid
λmax
225, 277, 283 nm
SMILES
COC1=CC=C(CC(C)N)C=C1.Cl
InChI Code
InChI=1S/C10H15NO.ClH/c1-8(11)7-9-3-5-10(12-2)6-4-9;/h3-6,8H,7,11H2,1-2H3;1H
InChI Key
VSHZXOLHFRVZND-UHFFFAOYSA-N
Schedule
I

Warning - this product is not for human or veterinary use.

Shipping & Storage
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Stability
≥ 2 years
Downloads & Resources
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Additional Information

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References & Product Citations
Product Description References

1. Staack, R.F., and Maurer, H.H. Metabolism of designer drugs of abuse Curr.Drug Metab. 6(3), 259-274 (2005).

2. Kraner, J.C., McCoy, D.J., Evans, M.A., et al. Fatalities caused by the MDMA-related drug paramethoxyamphetamine (PMA) J.Anal.Toxicol. 25(7), 645-648 (2001).

3. Martin-Iverson, M.T., Yamada, N., By, A.W., et al. "Designer" amphetamines: Effects on behavior and monoamines with or without reserpine and/or α-methyl-para-tyrosine pretreatment J. Psychiatr. Neurosci. 16(5), 253-261 (1991).

4. Tseng, L.F. 5-hydroxytryptamine uptake inhibitors block para-methoxyamphetamine-induced 5-HT release British Journal of Pharmacology 66(2), 185-190 (1979).

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