An Analytical Reference Material
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  • This product is qualified as a Reference Material that has been manufactured and tested to meet ISO/IEC 17025 and ISO 17034 international standards
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for qualified institutions; please contact our sales department for pricing
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Citalopram (hydrobromide)

Item No. 23252

Synonyms
Synonyms
  • Bonitrile
  • Lu 10-171B
  • Nitalapram
Technical Information
Formal Name
1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile, monohydrobromide
CAS Number
59729-32-7
Molecular Formula
C20H21FN2O • HBr
Formula Weight
Purity
≥98%
Formulation
A solid
SMILES
CN(C)CCCC1(C2=CC=C(F)C=C2)OCC3=CC(C#N)=CC=C31.Br
InChi Code
InChI=1S/C20H21FN2O.BrH/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20;/h4-9,12H,3,10-11,14H2,1-2H3;1H
InChi Key
WIHMBLDNRMIGDW-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Citalopram (hydrobromide) (Item No. 23252) is an analytical reference material categorized as an antidepressant.1,2,3 This product is intended for use in analytical forensic applications. This product is also available as a general research tool (Item No. 14572).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Millan, M.J., Gobert, A., Rivet, J.-M., et alMirtazapine enhances frontocortical dopaminergic and corticolimbic adrenergic, but not serotonergic, transmission by blockade of α2-adrenergic and serotonin2C receptors: A comparison with citalopram. Eur. J. Neurosci. 12(3), 1079-1095 (2000).

    2. Boothman, L.J., Mitchell, S.N., and Sharp, T. Investigation of the SSRI augmentation properties of 5-HT2 receptor antagonists using in vivo microdialysis. Neuropharmacology 50(6), 726-732 (2006).

    3. Bymaster, F.P., Zhang, W., Carter, P.A., et alFluoxetine, but not other selective serotonin uptake inhibitors, increases norepinephrine and dopamine extracellular levels in prefrontal cortex. Psychopharmacology (Berl) 160(4), 353-361 (2002).