3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol

Phentolamine Struktur
50-60-2
CAS-Nr.
50-60-2
Bezeichnung:
3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol
Englisch Name:
Phentolamine
Synonyma:
Fentolamine;regitine;3-(((4,5-Dihydro-1H-imidazol-2-yl)methyl)(p-tolyl)amino)phenol;dibasin;regitipe;Rogitine;c7337ciba;fentolamin;phentalamine;PHENTOLAMINE
CBNumber:
CB6665216
Summenformel:
C17H19N3O
Molgewicht:
281.35
MOL-Datei:
50-60-2.mol

3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol Eigenschaften

Schmelzpunkt:
174-175°
Siedepunkt:
424.02°C (rough estimate)
Dichte
1.0510 (rough estimate)
Brechungsindex
1.6500 (estimate)
storage temp. 
Hygroscopic, -20°C Freezer, Under inert atmosphere
Löslichkeit
DMSO (Slightly), Methanol (Slightly)
Aggregatzustand
Solid
pka
pKa 7.7 (Uncertain)
Farbe
Crystals
Stabilität:
Hygroscopic
CAS Datenbank
50-60-2(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Giftige Stoffe Daten 50-60-2(Hazardous Substances Data)
Toxizität LD50 orl-rat: 1250 mg/kg PSEBAA 71,70,49
Bildanzeige (GHS) Corrosion (GHS05)Exclamation Mark (GHS07)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H314 Verursacht schwere Verätzungen der Haut und schwere Augenschäden. Ätzwirkung auf die Haut Kategorie 1B Achtung P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
Sicherheit
P260 Dampf/Aerosol/Nebel nicht einatmen.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P330+P331 BEI VERSCHLUCKEN: Mund ausspülen. KEIN Erbrechen herbeiführen.
P303+P361+P353 BEI BERÜHRUNG MIT DER HAUT (oder dem Haar): Alle kontaminierten Kleidungsstücke sofort ausziehen. Haut mit Wasser abwaschen oder duschen.
P363 Kontaminierte Kleidung vor erneutem Tragen waschen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Phentolamine is also a derivative of imidazoline that exhibits a direct α-adrenoblocking, muscle-relaxant effect on smooth muscle as well as cholinomimetic, histamine, and sympathomimetic effects. The chemical variation of its structure permits a few of its properties to be more expressed. For example, the aforementioned tolazoline, 2-benzyl-2-imidazoline, a structural analog of phentolamine, has more of an expressed muscle-relaxant effect on smooth muscle than an α-adrenoblocking effect.

Verwenden

Anti-adrenergic.
Phentolamine is used to prevent or control hypertensive episodes that occurin patients with pheochromocytoma. It also has been used incombination with papaverine to treat impotence.

Definition

ChEBI: A substituted aniline that is 3-aminophenol in which the hydrogens of the amino group are replaced by 4-methylphenyl and 4,5-dihydro-1H-imidazol-2-ylmethyl groups respectively. An alpha-adrenergic antagonist, it is used fo the treatment of hypertension.

Indications

Human erectile tissue has a population of membrane receptors that are predominantly of the -adrenoceptor subtype. Phentolamine (Vasomax) is a nonselective - adrenoceptor blocking agent (see Chapter 11), and like other such agents, it has been used to treat ED. Nonselective adrenoceptor antagonists may provoke a reflex that increases both sympathetic outflow and the release of norepinephrine.

Allgemeine Beschreibung

Phentolamine isthe more effectiveα -blocker.

Mechanism of action

Its mechanism of action is as an α-adrenergic antagonist of both α1- and α2-receptors, causing vasodilation and reduction in peripheral resistance. When administered by intracavernosal injection, it is thought to cause relaxation of the cavernous smooth muscles and vasodilation of the penile arteries. This results in increased arterial blood flow into the corpus cavernosa as well as swelling and elongation of the penis. Venous outflow also is reduced, possibly as a result of increased venous resistance. Phentolamine is slowly released into venous circulation with minimal, if any, systemic effects. Time to peak effect is within 10 minutes, and duration of action when used with papaverine is 1 to 6 hours.

Clinical Use

Phentolamine has been used orally and intracavernosally in the treatment of ED. Following oral administration, phentolamine has a plasma half-life of about 30 minutes and a duration of action of 2 to 4 hours. An intracavernosal injection of phentolamine results in the drug reaching maximum serum levels in about 20 to 30 minutes. It is rapidly metabolized. Phentolamine has been used in combination with papaverine, chlorpromazine, and vasoactive peptides in the treatment of ED.

Nebenwirkungen

Side effects of phentolamine are dose related. It may cause orthostatic hypotension, reflex tachycardia, cardiac arrhythmias, and rarely, myocardial infarction. Phentolamine also may reduce sperm motility in vitro.

Sicherheitsprofil

Poison by subcutaneous, intravenous, and intraperitoneal routes. Moderately toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.

3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 107)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
LGM Pharma 1-(800)-881-8210
inquiries@lgmpharma.com United States 2110 70
S.Z. PhyStandard Bio-Tech. Co., Ltd. 0755-83725681-603
China 4484 50
Beijing HuaMeiHuLiBiological Chemical 010-56205725
waley188@sohu.com China 12323 58
Chengdu HuaXia Chemical Reagent Co. Ltd 400-1166-196 13458535857
cdhxsj@163.com China 13323 58
Finetech Industry Limited 027-87465837 19945049750
sales@finetechnology-ind.com China 9259 58
Shanghai YuanYe Biotechnology Co., Ltd. 18916372613
yanzihan@shyuanye.com China 87240 60
Amadis Chemical Company Limited 571-89925085
sales@amadischem.com China 131885 58
Guangdong wengjiang Chemical Reagent Co., Ltd. 0751-2886750 13927877953
3005811397@qq.com China 13280 58
Shandong Ono Chemical Co., Ltd. 0539-6362799 20)
China 10007 58
Jiaxing Deyi Chemical Co., Ltd. 86-0573-85866609 18367600069
945717149@qq.com China 9730 58

50-60-2(3-((4,5-Dihydro-1H-imidazol-2-yl)-methyl)(4-methyl-phenyl)amino)phenol)Verwandte Suche:


  • 2-((n-(m-hydroxyphenyl)-p-toluidino)methyl)-
  • 2-((n-(m-hydroxyphenyl)-p-toluidino)methyl)-2-imidazolin
  • 2-((n-(m-hydroxyphenyl)-p-toluidino)methyl)-2-imidazoline
  • AKOS NCG1-0052
  • AURORA KA-7803
  • PhentolamineMesilateBase
  • m-[N-[2-Imidazolin-2-ylmethyl]-p-toluidino] phenol
  • Phentolamine mesylas
  • phenotolamine
  • phentalamine
  • regitipe
  • PHENTOLAMINE
  • Regilin/Rartin/Phentolamine mesylate
  • Phenol, 3-[[(4,5-dihydro-1H-imidazol-2-yl)methyl](4-methylphenyl)amino]-
  • Rogitine
  • phentolaMine or its Mesylate
  • 3-(N-2-imidazolin-2-ylmethyl-p-toluidino)phenol
  • 3-[(4,5-dihydro-1h-imidazol-2-yl)methyl-(4-methylphenyl)-amino]phenol
  • Phentolamine Imp.
  • 2-(m-hydroxy-n-p-tolylanilinomethyl)-2-imidazoline
  • 2-(n-(m-hydroxyphenyl)-p-toluidinomethyl)imidazoline
  • 2-(n’-p-tolyl-n’-m-hydroxyphenylaminomethyl)-2-imidazoline
  • 3-(((4,5-dihydro-1h-imidazol-2-yl)methyl)(4-methylphenyl)amino)-pheno
  • c7337ciba
  • dibasin
  • fentolamin
  • m-(n-(2-imidazolin-2-ylmethyl)-p-toluidino)-pheno
  • Phentolamine Impurity
  • Phentolamine USP/EP/BP
  • regitine
  • 3-(((4,5-Dihydro-1H-imidazol-2-yl)methyl)(p-tolyl)amino)phenol
  • erectile dysfunction,inhibit,Adrenergic Receptor,orally active,insulin secretion,Phentolamine,Inhibitor,Beta Receptor
  • Phentolamine, 10 mM in DMSO
  • Fentolamine
  • 50-60-2
  • API
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