Clemastine fumarate
Synonym(s):Clemastine fumarate salt
- CAS NO.:14976-57-9
- Empirical Formula: C25H30ClNO5
- Molecular Weight: 459.96
- MDL number: MFCD00137486
- EINECS: 239-055-2
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-14 20:10:21
What is Clemastine fumarate?
Chemical properties
White Solid
Originator
Tavegyl,Sandoz,France,1967
The Uses of Clemastine fumarate
Clemastine fumarate is a selective histamine H1 receptor antagonist (Ki = 0.26 nM) that also displays high affinity for muscarinic receptors (Ki = 16 nM). It has also recently been identified as a positive allosteric modulator of P2X7 receptor signaling. Clemastine fumarate has long been used to inhibit histamine-induced bronchoconstriction in asthma and airway hyperresponsive studies.
The Uses of Clemastine fumarate
H1 Histamine receptor antagonist. Antihistaminic.
The Uses of Clemastine fumarate
anti-inflammatory
What are the applications of Application
Clemastine fumarate is a selective histamine H1 antagonist
Definition
ChEBI: The fumaric acid salt of clemastine. An antihistamine with antimuscarinic and moderate sedative properties, it is used for the symptomatic relief of allergic conditions such as rhinitis, urticaria, conjunctivitis and in pruritic (severe itching) skin condi ions.
Manufacturing Process
9.9 g of α-methyl-p-chlorobenzhydrol are added to a suspension of 2.3 g of powdered sodamide in 30 cc of benzene. Subsequently 7.4 g of Nmethylpyrrolidyl-(2)-ethyl chloride are added and the solution is heated to the boil at reflux for 20 hours. Then shaking is first effected with water and then 4 times each time with 25 cc of 2 N hydrochloric acid. The acid extracts are made alkaline with potassium hydroxide solution while cooling strongly, and the precipitated oil is extracted with ether. After drying of the ethereal solution over potassium carbonate, the solvent is evaporated and the residue is fractionally distilled in a high vacuum, whereby N-methyl-2-[2'-(α-methyl-pchlorobenzhydryloxy)-ethyl]-pyrrolidine boils over at 154°C/0.02 mm Hg. The base is converted to the fumarate by reaction with fumaric acid.
brand name
Tavist (Novartis).
Therapeutic Function
Antihistaminic
General Description
Dextrorotatory clemastine, R,R-2[2[1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1- methylpyrrolidine hydrogen furnarate (1:1) (Tavist), has two chiral centers, each of which has the (R) absolute configuration. A comparison of the activities of the enantiomers indicates that the asymmetric center close to the terminal side chain nitrogen is of lesser importance to antihistaminic activity.
? This member of the ethanolamine series is characterized by a long duration of action, with an activity that reaches a maximum in 5 to 7 hours and persists for 10 to 12 hours. It is well absorbed when administered orally, and it is excreted primarily in the urine. The side effects are those usually encountered with this series of antihistamines. Clemastine is closely related to chlorphenoxamine, which is used for its central cholinergic-blocking activity. Therefore, it is not surprising that clemastine has significant antimuscarinic activity.
Biological Activity
H 1 -receptor antagonist. Clinically-used antihistamine.
Biochem/physiol Actions
Clemastine fumarate is an antihistamine H1-antagonist and anticholinergic that also has antipruritic activity.
Veterinary Drugs and Treatments
Clemastine may be used for symptomatic relief of histamine1-related allergic conditions.
storage
Store at RT
Properties of Clemastine fumarate
Melting point: | 158-162°C |
Boiling point: | 154°C (rough estimate) |
alpha | D21 +16.9° (methanol) |
Density | 1.0247 (rough estimate) |
refractive index | 1.5790 (estimate) |
storage temp. | 2-8°C |
solubility | DMSO: soluble5mg/mL (clear solution; warmed) |
form | powder |
color | white to beige |
optical activity | [α]/D +15 to +25°, c = 1 in methanol |
CAS DataBase Reference | 14976-57-9(CAS DataBase Reference) |
Safety information for Clemastine fumarate
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H302:Acute toxicity,oral |
Precautionary Statement Codes |
P280:Wear protective gloves/protective clothing/eye protection/face protection. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for Clemastine fumarate
InChIKey | PMGQWSIVQFOFOQ-YKVZVUFRSA-N |
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION INOSITOL PANTOPRAZOLE SODIUM SESQUIHYDRATE Metformin FLUCLOXACILLIN SODIUM STERILE NIMESULIDE BP ZONISAMIDE 1,1-Dimethylethyl 4-(2-azidoacetyl)-1-piperidinecarboxylate 2-Bromo-1-(bromomethyl)-3-iodo-5-nitrobenzene 1,2-Dibromo-3-(bromomethyl)-5-nitrobenzene 2-Cyano-5-pyrimidineacetonitrile 7-Fluoro-4-cinnolinamine 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzeneRelated products of tetrahydrofuran
You may like
-
Clemastine fumarate 95% CAS 14976-57-9View Details
14976-57-9 -
Clemastine fumarate CAS 14976-57-9View Details
14976-57-9 -
1823754-06-8 98%View Details
1823754-06-8 -
2-Chloro-5-(iodomethyl)pyrimidine 2268818-88-6 98%View Details
2268818-88-6 -
2092793-98-9 98%View Details
2092793-98-9 -
1360944-55-3 7-Methoxy-1H-indol-5-amine 98%View Details
1360944-55-3 -
2090480-14-9 98%View Details
2090480-14-9 -
1-Methyl 2-bromo-5-[(1-carboxy-1-methylethyl)amino]benzoate 1651844-56-2 98%View Details
1651844-56-2