Citalopram Hydrobromide

Citalopram hydrobromide is an orally administered selective serotonin reuptake inhibitor (SSRI) with a chemical structure unrelated to that of other SSRIs or of tricyclic, tetracyclic, or other available antidepressant agents.

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Raw Hormone Powder Citalopram Hydrobromide For Antidepressant


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Citalopram Hydrobromide Basic Info


Product NameCitalopram Hydrobromide
AliasCelexa, citalopram HBr
CAS59729-32-7
MFC20H22BrFN2O
MW405.3
EINECS261-890-6
Assay99.0%
PHYSICAL STATEwhite crystalline powder
UsageTreatment of depression
StorageStore in cool and dry places, keep away from strong light
Package methodshundreds of disgusied pacakges
After-sales serviceWarm after-sale service for you 24/7. Any of your question would be solved for the first as soon as possible.
Shipping methodFedEx,UPS,DHL,EMS, Fedex and so on, by air or sea.Will choose the best shipping way.
Delivery timedelivery quickly at the day when receive the payment, will be deliveried in 4-7days after tracking
Payment MethodsWestern union, money gram, bitcoin and bank transfer


Citalopram Hydrobromide Descrption


Citalopram hydrobromide is an orally administered selective serotonin reuptake inhibitor (SSRI) with a chemical structure unrelated to that of other SSRIs or of tricyclic, tetracyclic, or other available antidepressant agents. Citalopram Hydrobromide is a racemic bicyclic phthalane derivative designated (±)-1-(3-dimethylaminopropyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile. Citalopram is an antidepressant drug of the selective serotonin reuptake inhibitor (SSRI) class. 


Citalopram Hydrobromide Application


Citalopram hydrobromide (citalopram HBr) is an orally administered selective serotonin reuptake inhibitor (SSRI) with a chemical structure unrelated to that of other SSRIs or of tricyclic, tetracyclic, or other available antidepressant agents.


citalopram is a highly selective serotonin reuptake inhibitor (SSRI) with minimal effects on norepinephrine (NE) and dopamine (DA) neuronal reuptake. Tolerance to the inhibition of 5-HT uptake is not induced by long-term (14 day) treatment of rats with citalopram. Citalopram is a racemic mixture (50/50), and the inhibition of 5-HT reuptake by citalopram is primarily due to the (S)-enantiomer.


The advantage of Citalopram hydrobromide is that it has no effect on cholinergic muscarinic receptors, histamine receptors and α-adrenergic receptors . Because if these receptors are inhibited, a lot of side effects caused by antidepressants will produce, such as dry mouth, sedation, orthostatic hypotension.Citalopram hydrobromide is effective for not only endogenous depression patients but also non-endogenous depression patients. Its antidepressant effect is usually established after 2-4 weeks .


Citalopram hydrobromide does not affect the cardiac conduction system and blood pressure, which is particularly important for elderly patients.


Citalopram Hbr


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