Azelastine

Azelastine Basic information
Product Name:Azelastine
Synonyms:1(2h)-phthalazinone,4-((4-chlorophenyl)methyl)-2-(hexahydro-1-methyl-1h-azepin;4-(p-chlorobenzyl)-2-(hexahydro-1-methyl-1h-azepin-4-yl)-1-(2h)-phthalazinon;4-(4-chlorobenzyl)-2-(1-methylazepan-4-yl)phthalazin-1(2H)-one hydrochloride;4-(4-chlorobenzyl)-2-(1-methylazepan-4-yl)phthalazin-1-one;4-[(4-chlorophenyl)methyl]-2-(1-methyl-4-azepanyl)-1-phthalazinone;4-[(4-chlorophenyl)methyl]-2-(1-methylazepan-4-yl)phthalazin-1(2H)-one;Azelastinum [INN-Latin];KBio3_002992
CAS:58581-89-8
MF:C22H24ClN3O
MW:381.9
EINECS:253-720-4
Product Categories:TELAZOL;API
Mol File:58581-89-8.mol
Azelastine Structure
Azelastine Chemical Properties
Melting point 111 - 115°C
Boiling point 533.9±60.0 °C(Predicted)
density 1.1505 (rough estimate)
refractive index 1.5790 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly, Heated), Methanol (Slightly)
form Solid
pkapKa 9.82(H2O t=25 I=0.025) (Uncertain)
color White to Off-White
BCS Class1?
Stability:Stable under recommended storage conditions., Stable Under Recommended Storage C
CAS DataBase Reference58581-89-8(CAS DataBase Reference)
Safety Information
Hazardous Substances Data58581-89-8(Hazardous Substances Data)
ToxicityLD50 orl-rat: 310 mg/kg ARZNAD 31,1184,81
MSDS Information
Azelastine Usage And Synthesis
Usesanesthetic, anticonvulsant
DefinitionChEBI: A phthalazine compound having an oxo substituent at the 1-position, a 1-methylazepan-4-yl group at the 2-position and a 4-chlorobenzyl substituent at the 4-position.
Brand nameAstelin (Medpointe); Optivar (Medpointe).
Clinical UseAzelastine, although not a close structural analogue to the benzimidazoles, has some structural similarities to them. It is used as a nasal spray for allergic rhinitis and as eye drops for allergic conjunctivitis.Like olopatadine, azelastine also stabilizes mast cells, preventing degranulation and subsequent release of histamine, leukotrienes, and PGD2. It is available in Europe for systemic use in the treatment of asthma and seasonal allergies. Besides antihistaminic effects, it also may block release of histamine and other inflammatory mediators from mast cells. When administered orally, the N-dealkylated metabolite appears to contribute significantly to its pharmacological effects.
Safety ProfilePoison by ingestion,subcutaneous, intravenous, and intraperitoneal routes.Experimental reproductive effects. When heated todecomposition it emits toxic fumes of NOx and Cl- .
Methylparaben Methyl Bensulfuron methyl Parathion-methyl Phenylacetone Sibutramine hydrochloride Tramadol hydrochloride 2,6-DIMETHYLNAPHTHALENE 2-Methylnaphthalene Azelastine Kresoxim-methyl DBU 1-AdaMantanethylaMine Thiophanate-methyl Methyl acrylate Methyl acetate Methyl bromide METHYL THIOPHENE-2-CARBOXYLATE

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