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2,4,6-Trimethoxyamphetamine (hydrochloride)

Item No. 12099

Restricted Product (Schedule I)
Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • TMA-6
Technical Information
Formal Name
2,4,6-trimethoxy-α-methyl-benzeneethanamine, monohydrochloride
CAS Number
23815-74-9
Molecular Formula
C12H19NO3 • HCl
Formula Weight
261.7
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 13 mg/mlDMSO: 5 mg/mlEthanol: 14 mg/mlPBS (pH 7.2): 10 mg/ml
SMILES
COC1=CC(OC)=C(CC(C)N)C(OC)=C1.Cl
InChi Code
InChI=1S/C12H19NO3.ClH/c1-8(13)5-10-11(15-3)6-9(14-2)7-12(10)16-4;/h6-8H,5,13H2,1-4H3;1H
InChi Key
HAIHNGCKJFYVFH-UHFFFAOYSA-N
Regulatory Information
DEA Schedule
I
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    5 mg

    $90

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    Cayman Chemical
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    Product Description

    The trimethoxyamphetamines (TMA) are a family of designer drugs developed on an amphetamine base. TMA-6, known more formally as 2,4,6-trimethoxyamphetamine, is a psychedelic hallucinogen which has appeared on the illicit drug market.1,2 Unlike amphetamines and cathinones, TMA-6 has no effect on the release or re-uptake of monoamines (dopamine, serotonin, and norepinephrine).3 This product is intended for research and forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Nieddu, M., Boatto, G., Pirisi, M.A., et al. LC-MS analysis of trimethoxyamphetamine designer drugs (TMA series) from urine samples. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 867(1), 126-130 (2008).

    2. Wohlfarth, A., Weinmann, W., and Dresen, S. LC-MS/MS screening method for designer amphetamines, tryptamines, and piperazines in serum. Anal. Bioanal. Chem. 396(7), 2403-2414 (2010).

    3. Nagai, F., Nonaka, R., and Satoh Hisashi Kamimura, K. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. Eur. J. Pharmacol. 559(2-3), 132-137 (2007).