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Tamsulosin hydrochloride

Basic information Safety Supplier Related

Tamsulosin hydrochloride Basic information

Product Name:
Tamsulosin hydrochloride
Synonyms:
  • Tamsulosinehydrochloride
  • Benzenesulfonamide, 5-[2-[[2-(2-ethoxyphenoxy)ethyl]amino]propyl]-2-methoxy-, monohydrochloride (9CI)
  • dl-Tamsulosin hydrochloride
  • (-)-(R)-5-[2-[2-(2-Ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide hydrochloride
  • Tamsulosin hydrochloride
  • Tamuzosin hydrochloride
  • EC-617
  • Racemic Tamsulosin Hydrochloride (50 mg)
CAS:
80223-99-0
MF:
C20H29ClN2O5S
MW:
444.97
Product Categories:
  • Intermediates & Fine Chemicals
  • Isotope Labelled Compounds
  • Pharmaceuticals
Mol File:
80223-99-0.mol
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Tamsulosin hydrochloride Chemical Properties

Melting point:
254-256 °C
solubility 
DMSO (Slightly), Methanol (Slightly), Water (Slightly)
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Safety Information

HS Code 
2935909550
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Tamsulosin hydrochloride Usage And Synthesis

Chemical Properties

White to Off-White Solid

Uses

Tamsulosin is a specific α1-adrenoceptor antagonist. Used in the treatment of benign prostatic hypertrophy.

Uses

Tamsulosin hydrochloride is a specific ;1-adrenoceptor antagonist. Used in the treatment of benign prostatic hypertrophy.

Clinical Use

Treatment of benign prostatic hyperplasia

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Antidepressants: enhanced hypotensive effect with MAOIs.
Antifungals: concentration increased by ketoconazole.
Avanafil, vardenafil, sildenafil and tadalafil: enhanced hypotensive effect, avoid concomitant use.
Beta-blockers: enhanced hypotensive effect; increased risk of first dose hypotensive effect.
Calcium-channel blockers: enhanced hypotensive effect; increased risk of first dose hypotensive effect.
Diuretics: enhanced hypotensive effect; increased risk of first dose hypotensive effect.
Moxisylyte: possibly severe postural hypotension.

Metabolism

Tamsulosin is metabolised slowly in the liver primarily by the cytochrome P450 isoenzymes CYP2D6 and CYP3A4; it is excreted mainly in the urine as metabolites and some unchanged drug

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