S-(+)-Chlorpheniramine maleate salt
SIGMA/C4915
Synonym: (S)-γ-(4-Chlorophenyl)-N,N-dimethyl-2-pyridinepropanamine maleate salt
CAS Number: 2438-32-6
Empirical Formula (Hill Notation): C16H19ClN2 · C4H4O4
Molecular Weight: 390.86
EC Number: 219-450-6
MDL Number: MFCD00079046
Linear Formula: C16H19ClN2 · C4H4O4
Product Type: Chemical
| form | powder |
| InChI | 1S/C16H19ClN2.C4H4O4/c1-1 |
| InChI key | DBAKFASWICGISY-DASCVMRKSA |
| originator | Bayer |
| Quality Level | 200 ![]() |
| SMILES string | [H]C(=C(/[H])C(O)=O)C(O) |
| Application: | S-(+)-Chlorpheniramine maleate salt has been used to study the anticholinergic effect of Achillea millefolium and Portulaca olerace on muscarinic receptors of guinea pig tracheal smooth muscle. |
| Biochem/physiol Actions: | H1 histamine receptor antagonist; active isomer. Chlorpheniramine maleate is clinically used as a topical ointment to treat skin disorders such as sunburn, urticaria, angioedema, pruritus and insect bites. |
| Features and Benefits: | This compound is featured on the Histamine Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here . |
| Features and Benefits: | This compound was developed by Bayer . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here . |
| General description: | Chlorpheniramine maleate is a cationic amphiphilic anti-histamine agent, which is composed of a hydrophobic ring structure and a hydrophilic side chain with a charged cationic amino group. |
| Packaging: | 1, 5 g in glass bottle |
| Symbol | GHS06 |
| Signal word | Danger |
| Hazard statements | H301 |
| Precautionary statements | P301 + P310 |
| Hazard Codes | T |
| Risk Statements | 25 |
| Safety Statements | 36/37/39-45 |
| RIDADR | UN 2811 6.1 / PGIII |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| UNSPSC | 12352116 |


