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Chlorpheniramine is a first generation alkylamine antihistamine that inhibits H1 histamine receptors, serotonin transporters (SERT), and norepinephrine transporters (NET); it exhibits anti-allergic and antidepressant activities. Chlorpheniramine is clinically used to treat allergic rhinitis and urticaria. In animal models, chlorpheniramine displays some modulation of memory consolidation.
| Cas No. | 113-92-8 |
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| Purity | ≥98% |
| Formula | C16H19ClN2 • C4H4O4 |
| Formula Wt. | 390.87 |
| Chemical Name | ψ-(4-Chlorophenyl)-N,N-dimethyl-2-pyridine- propanamine Maleate |
| IUPAC Name | (Z)-but-2-enedioic acid;3-(4-chlorophenyl)-N,N-dimethyl-3-pyridin-2-ylpropan-1-amine |
| Synonym | Allergisan, Anntagonate, Cloropiril, Histadur, Lorphen, Teldrin |
| Melting Point | 130-135°C |
| Solubility | Soluble in water (250 mg/mL) and ethanol (100 mg/mL). |
| Appearance | White crystalline powder |
| Store Temp | Ambient |
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| Ship Temp | Ambient |
| MSDS | |
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| Info Sheet |
Gianlorenço AC, Serafim KR, Canto-de-Souza A, et al. Emotional memory consolidation impairment induced by histamine is mediated by H1 but not H2 receptors. Brain Res Bull. 2012 Dec 1;89(5-6):197-202. PMID: 22986235.
Hellbom E. Chlorpheniramine, selective serotonin-reuptake inhibitors (SSRIs) and over-the-counter (OTC) treatment. Med Hypotheses. 2006;66(4):689-90. PMID: 16413139.
