Detail of > 63-92-3
- MSDS Download

- CAS Number:
- 63-92-3
- Name:
Benzenemethanamine,N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-, hydrochloride (1:1)
- Superlist Name:
- Phenoxybenzamine hydrochloride
- Formula:
- C18H22 Cl N O . Cl H
- Molecular Structure:

- Synonyms:
- Benzenemethanamine,N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-, hydrochloride (9CI);Benzylamine, N-(2-chloroethyl)-N-(1-methyl-2-phenoxyethyl)-, hydrochloride(7CI,8CI); 2-(N-Benzyl-2-chloroethylamino)-1-phenoxypropane hydrochloride;Dibenzylin; Dibenzyline chloride; Dibenzyline hydrochloride; Dibenzyran; N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzylamine,hydrochloride; N-2-Phenoxyisopropyl-N-benzyl-b-chloroethylamine hydrochloride; NSC 37448;Phenoxybenzamine chloride; Phenoxybenzamine hydrochloride
- Molecular Weight:
- 340.32
- EINECS:
- 200-569-7
- Melting Point:
- 137.5 ºC
- Boiling Point:
- 381.5 °C at 760 mmHg
- Flash Point:
- 184.5 °C
- Solubility:
- <0.01 g/100 mL at 18.5 ºC in water
- Hazard Symbols:

- Risk Codes:
- R22;R40
- Safety:
- Confirmed carcinogen with experimental carcinogenic and teratogenic data. Poison by intraperitoneal, intravenous, and subcutaneous routes. Human systemic effects by ingestion: changes in tubules, including acute renal failure, acute tubular necrosis. Moderately toxic by ingestion. Other experimental reproductive effects. Mutation data reported. A long-acting adrenergic blocker. When heated to decomposition it emits very toxic fumes of NOx and Cl−.Details
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Reference
- The effect of
- The effect of .beta.-adrenergic substances on exocrine pancreatic function. Studies in the isolated perfused cat pancreas. Heidbreder, E.; Sieber, P.; Heidland, A. (Med. Universitaetsklin. Wuerzburg, Wuerzburg, Ger.). Res. Exp. Med., 171(1), 79-92 (German) 1977. CODEN: REXMAS. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) The .beta.-sympathomimetics, isoproterenol sulfate [299-95-6], orciprenaline sulfate [5874-97-5], salbutamol [18559-94-9], fenoterol-HBr [1944-12-3], and terbutaline sulfate [23031-32-5], increased protein and enzyme secretion by isolated cat pancreas but did not affect the excretion of Ca into the juice or the rate of vol. output. The sympatholytics, phentolamine-HCl [73-05-2], phenoxybenzamine-HCl [63-92-3], L-propranolol-HCl [4199-10-4], D-propranolol-HCl [13071-11-9], prindolol [13523-86-9], oxprenolol-HCl [6452-73-9], practolol [6673-35-4], and butoxamine-HCl [5696-15-1], inhibited pancreatic enzyme and protein secretion. Tetracaine-HCl [136-47-0], atropine sulfate [55-48-1], and hemicholinium [16478-59-4] also inhibited pancreatic protein and enzyme secretion. Pretreatment with reserpine or 6-hydroxydopamine did not inhibit the pancreas response to the sympathomimetics, indicating that they influence pancreatic protein and enzyme secretion in a cholinergic way.
- Selectivity of blocking agents for pre- and postsynaptic
- Selectivity of blocking agents for pre- and postsynaptic .alpha.-adrenoceptors. Doxey, J. C.; Smith, C. F. C.; Walker, Julie M. (Pharm. Div., Reckitt Colman, Hull, Engl.). Br. J. Pharmacol., 60(1), 91-6 (English) 1977. CODEN: BJPCBM. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Low frequency (0.1 Hz) elec. stimulation of isolated rat vas deferens produced regular contractions that were inhibited by low concns. of clonidine-HCl [4205-91-8]. Clonidine inhibition was presynaptic in origin and involved .alpha.-adrenoceptors. Yohimbine-HCl [65-19-0] (100 ng/mL) and phentolamine mesylate [65-28-1] (100 ng/mL) were more potent in blocking presynaptic than postsynaptic .alpha.-adrenoceptors. Phenoxybenzamine-HCl [63-92-3] (100 ng/mL) and prazosin-HCl [19237-84-4] (10 ng/mL) blocked postsynaptic .alpha.-adrenoceptors preferentially.In this article, certain chemicals are used. One of their cas registry numbers is 32808-09-6 Presynaptic and postsynaptic .alpha.-adrenoceptors differ in their sensitivity to .alpha.-adrenoceptor antagonists. .
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