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Unlabeled Version(s)
9001142Norsufentanil
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Norsufentanil-d3

Item No. 9001143

Synonyms
Synonyms
  • R 30451-d3
Technical Information
Formal Name
N-[4-(methoxy-d3-methyl)-4-piperidinyl]-N-phenyl-propanamide
CAS Number
1204688-16-3
Molecular Formula
C16H21D3N2O2
Formula Weight
Purity
≥99% deuterated forms (d1-d3)
Formulation
A solution in methyl acetate
DMF: 30 mg/mlDMSO: 20 mg/mlEthanol: 30 mg/mlPBS (pH 7.2): 0.16 mg/ml
SMILES
O=C(CC)N(C1=CC=CC=C1)C2(COC([2H])([2H])[2H])CCNCC2
InChi Code
InChI=1S/C16H24N2O2/c1-3-15(19)18(14-7-5-4-6-8-14)16(13-20-2)9-11-17-12-10-16/h4-8,17H,3,9-13H2,1-2H3/i2D3
InChi Key
ULOZGJWEIWAWML-BMSJAHLVSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Norsufentanil-d3 contains three deuterium atoms. It is intended for use as an internal standard for the quantification of norsufentanil by GC- or LC-mass spectrometry. Sufentanil is a powerful synthetic opioid analgesic that is used in anesthesia and palliative care.1,2,3 Norsufentanil is a metabolite of sufentanil, produced by oxidative N-dealkylation in the liver by cytochrome P450 isoforms.4 The physiological and toxicological properties of this compound are unknown. This product is intended for forensic applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Bovill, J.G., Sebel, P.S., and Stanley, T.H. Opioid analgesics in anesthesia: With special reference to their use in cardiovascular anesthesia. Anesthesiology 61(6), 731-755 (1984).

    2. Hodgson, P.S., Neal, J.M., Pollock, J.E., et alThe neurotoxicity of drugs given intrathecally (spinal). Anesth. Analg. 88(4), 797-809 (1999).

    3. King, S., Forbes, K., Hanks, G.W., et alA systematic review of the use of opioid medication for those with moderate to severe cancer pain and renal impirment: A European Palliative Care Research Collaborative opioid guidelines project. Palliat. Med. 25(5), 525-552 (2011).

    4. Tateishi, T., Krivoruk, Y., Ueng, Y.F., et alIdentification of human liver cytochrome P-450 3A4 as the enzyme responsible for fentanyl and sufentanil N-dealkylation. Anesth. Analg. 82(1), 167-172 (1996).