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(±)-Methamphetamine-d9 (hydrochloride)

Item No. 22836

Restricted Product (Schedule II)
Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • DL-Methamphetamine-d9
Technical Information
Formal Name
N,α-di(methyl-d3)-benzeneethan-α,β,β-d3-amine, monohydrochloride
CAS Number
1219805-48-7
Molecular Formula
C10H6D9N • HCl
Formula Weight
194.8
Purity
≥99% deuterated forms (d1-d9)
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 3 mg/mlDMSO: 5 mg/mlEthanol: 20 mg/mlPBS (pH 7.2): 3 mg/ml
SMILES
[2H]C(NC([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])C1=CC=CC=C1.Cl
InChi Code
InChI=1S/C10H15N.ClH/c1-9(11-2)8-10-6-4-3-5-7-10;/h3-7,9,11H,8H2,1-2H3;1H/i1D3,2D3,8D2,9D;
InChi Key
TWXDDNPPQUTEOV-XJZPAETNSA-N
Regulatory Information
DEA Schedule
II
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    (±)-Methamphetamine-d9 (hydrochloride) (Item No. 22836) is intended for use as an internal standard for the quantification of (±)-methamphetamine (Item Nos. ISO60168 | 36566) by GC- or LC-MS. Methamphetamine is categorized as an amphetamine and consists of dextrorotary and levorotary enantiomers.1,2 (+)-Methamphetamine (Item No. 13997) is the more physiologically active isomer compared with (–)-methamphetamine (Item No. 13998). Methamphetamine is both neurotoxic and frequently abused.3 (±)-Methamphetamine-d9 is regulated as a Schedule II compound in the United States. 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. Jirovsky, D., Lemr, K., Sevcík, J., et al. Methamphetamine - properties and analytical methods of enantiomer determination. Forensic Sci. Int. 96(1), 61-70 (1998).

    2. Rothman, R.B., Baumann, M.H., Dersch, C.M., et al. Amphetamine-type central nervous system stimulants release norepinephrine more potently than they release dopamine and serotonin. Science 39(1), 32-41 (2001).

    3. Yu, S., Zhu, L., Shen, Q., et al. Recent advances in methamphetamine neurotoxicity mechanisms and its molecular pathophysiology. Behav. Neurol. 103969 (2015).