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Chemodex
Trazodone hydrochloride
As low as
45
CHF
CHF 45.00
In stock
Only %1 left
CDX-T0476-G0011 gCHF 45.00
CDX-T0476-G0055 gCHF 103.00
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Product Details | |
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Synonyms | 2-[3-[4-(3-Chlorophenyl)-1-piperazinyl]propyl]-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one hydrochloride; AF 1161; Desyrel; Molipaxin; KB 831; Pragmazone; Thombran; Trazolan; Tombran; Trittico; Bimaran; Mesyrel |
Product Type | Chemical |
Properties | |
Formula | C19H22ClN5O . HCl |
MW | 408.32 |
CAS | 25332-39-2 |
RTECS | XZ5660000 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥99% (HPLC) |
Appearance | White to off-white powder. |
Solubility | Soluble in DMSO (10mg/ml), methanol (10mg/ml) or water (1mg/ml). |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | OHHDIOKRWWOXMT-UHFFFAOYSA-N |
Smiles | ClC1=CC=CC(N(CC2)CCN2CCCN3N=C(C=CC=C4)N4C3=O)=C1.Cl |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +4°C |
Long Term Storage | -20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at -20°C. |
Documents | |
Product Specification Sheet | |
Datasheet |
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Description
Trazodone hydrochloride belongs to the class of serotonin receptor antagonists and reuptake inhibitors (SARIs). Trazodone hydrochloride has anti-depressant and neuroprotectant activity. Trazodone hydrochloride exerts antagonistic properties against α1- and α2-adrenergic receptors and histamine H1 receptors, with minimal anticholinergic effects. Shown to enhance neuronal differentiation of mouse and human neural progenitor cells. Also inhibits PERK/eIF2α-P-mediated reduction in protein synthesis and restores memory deficits in a mouse dementia model. Its broad pharmacological activity makes it a valuable tool in both neuroscience research and therapeutic development. Can be used as a reference compound.
Product References
(1) A. Georgotas, et al.; Pharmacotherapy 2, 255 (1982) | (2) S.G. Bryant & L. Ereshefsky; Clin. Pharm. 1, 406 (1982) | (3) A. Fagiolini, et al.; Review CNS Drugs 26, 1033 (2012) | (4) M. Halliday, et al.; Brain 140, 1768 (2017) | (5) V. Bortolotto, et al.; ACS Chem. Neurosci. 8, 2027 (2017)