Inquire About a Product| Product: | Venlafaxine HCl | ||||||||
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| Catalog Number: | 5552 | ||||||||
| CAS Number: | 99300-78-4 | ||||||||
| Synonyms: |
(±)-1-[2-(Dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexanol hydrochloride; Effexor |
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| Pricing: |
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| Formula: | C17H27NO2 • HCl | ||||||||
| Chemical Purity: | >98% | ||||||||
| Molecular Weight: | 313.86 | ||||||||
| Structure: |
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| Appearance: | Powder | ||||||||
| Category: | Unlabeled Reference Standards | ||||||||
| Stability: | Stable under recommended storage conditions | ||||||||
| Storage: |
Keep container tightly closed in a dry and well ventilated place. Light sensitive |
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| Transportation: |
Non-hazardous for transport |
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| Literature References: |
Berrocoso, E., and Mico, J.A., In vivo effect of venlafaxine on locus coeruleus neurons: role of opioid, α2-adrenergic and 5-HT1A receptors. J. Pharmacol. Exp. Ther., (2007); Merck 14,9946 |
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| MSDS: | |||||||||
| Description: |
Venlafaxine is an antidepressant. The mechanism of the antidepresant action of venlafaxine in humans is associated with its potentiation of neurotransmitter activity in the CNS. Venlafaxine is a potent inhibitor of neuronal serotonin and norepinephrine reuptake and weak inhibitor of dopamine reuptake. Venlafaxine has no significant activity for muscarinic, histaminergic, or α-1 adrenergic receptors in vitro. Venlafaxine does not possess MAO inhibitor activity. |