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Technical Information
Formal Name
3,4-dichloro-N-((1-(dimethylamino)cyclohexyl)methyl)benzamide-2,5,6-d3
CAS Number
2416676-30-5
Molecular Formula
C16H19Cl2D3N2O
Formula Weight
Purity
≥99% deuterated forms (d1-d3)
Formulation
A crystalline solid
Chloroform: 10 mg/ml
λmax
238 nm
SMILES
ClC1=C(Cl)C([2H])=C([2H])C(C(NCC2(N(C)C)CCCCC2)=O)=C1[2H]ClC1=C(Cl)C([2H])=C([2H])C(C(NCC2(N(C)C)CCCCC2)=O)=C1[2H]
InChi Code
InChI=1S/C16H22Cl2N2O/c1-20(2)16(8-4-3-5-9-16)11-19-15(21)12-6-7-13(17)14(18)10-12/h6-7,10H,3-5,8-9,11H2,1-2H3,(H,19,21)/i6D,7D,10D
InChi Key
JMZROFPPEXCTST-OFTYRWGKSA-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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    Product Description

    AH 7921-d3 (Item No. 33723) is intended for use as an internal standard for the quantification of AH 7921 (Item Nos. 19732 | 12036) by GC- or LC-MS. AH 7921 is categorized as an opioid.1 It is an analgesic with high addictive liability in animal models.2,3 AH 7921-d3 is regulated as a Schedule I 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. Hayes, A.G., and Tyers, M.B. Determination of receptors that mediate opiate side effects in the mouse. Br. J. Pharmacol. 79(3), 731-736 (1983).

    2. Brittain, R.T., Kellett, D.N., Neat, M.L., et alProceedings: Anti-nociceptive effects in N-substituted cyclohexylmethylbenzamides. Br. J. Pharmacol. 49(1), 158P-159P (1973).

    3. Cha, H.J., Jeon, S.Y., Jang, H.J., et alRewarding and reinforcing effects of 4-chloro-2,5-dimethoxyamphetamine and AH-7921 in rodents. Neurosci. Lett. 676, 66-70 (2018).