Haloperidol decanoate

CAT:
804-HY-107969-01
Size:
5 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Haloperidol decanoate - image 1

Haloperidol decanoate

  • Description:

    Haloperidol decanoate is a depot preparation of haloperidol, a commonly used butyrophenone derivative with antipsychotic activity. Haloperidol decanoate can increase the striatal D2 receptor in rat. Haloperidol decanoate can improve conditions of psychoses (mainly schizophrenia) . Haloperidol decanoate can lead to increased accumulation of the dopamine metabolites homo-vanillic acid. Haloperidol decanoate can reduce intestinal transport, increase gastric emptying and reduce acid output in rat model[1][4].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H413
  • Target:

    COX; Dopamine Receptor; NO Synthase
  • Type:

    Reference compound
  • Related Pathways:

    GPCR/G Protein; Immunology/Inflammation; Neuronal Signaling
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Neurological Disease; Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/haloperidol-decanoate.html
  • Purity:

    99.67
  • Solubility:

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles:

    CCCCCCCCCC (OC1 (C2=CC=C (Cl) C=C2) CCN (CCCC (C3=CC=C (F) C=C3) =O) CC1) =O
  • Molecular Formula:

    C31H41ClFNO3
  • Molecular Weight:

    530.11
  • Precautions:

    H302, H413
  • References & Citations:

    [1]R Beresford, et al. Haloperidol decanoate. A preliminary review of its pharmacodynamic and pharmacokinetic properties and therapeutic use in psychosis. Drugs. 1987 Jan;33 (1) :31-49.|[2]Schmitz, I., et al., (2025) . A single dose of haloperidol decanoate induces short-term hippocampal neuroinflammation: focus on the glial response. Pharmacological reports : PR, 77 (3), 800–808. |[3]Oh-e, Y., et al., (1991) . Pharmacokinetics of haloperidol decanoate in rats. Journal of pharmacobio-dynamics, 14 (11), 615–622.|[4]Akiyama, K., et al., (1987) . Effect of chronic administration of haloperidol (intermittently) and haloperidol-decanoate (continuously) on D2 dopamine and muscarinic cholinergic receptors and on carbachol-stimulated phosphoinositide hydrolysis in the rat striatum. The Japanese journal of psychiatry and neurology, 41 (2), 311–320.
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

    -20°C, 3 years (Powder)
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • CAS Number:

    74050-97-8